<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1405-9940</journal-id>
<journal-title><![CDATA[Archivos de cardiología de México]]></journal-title>
<abbrev-journal-title><![CDATA[Arch. Cardiol. Méx.]]></abbrev-journal-title>
<issn>1405-9940</issn>
<publisher>
<publisher-name><![CDATA[Instituto Nacional de Cardiología Ignacio Chávez]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-99402005000100007</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Análisis de la utilidad de ecocardiografía de contraste y medicina nuclear en afección cardiovascular de origen autoinmune]]></article-title>
<article-title xml:lang="en"><![CDATA[Analysis of the usefulness of contrast echocardiography and nuclear medicine in cardiovascular affection due to autoimmune diseases]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Espinóla Zavaleta]]></surname>
<given-names><![CDATA[Nilda]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Alexánderson]]></surname>
<given-names><![CDATA[Erick]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Soto]]></surname>
<given-names><![CDATA[María Elena]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Flores]]></surname>
<given-names><![CDATA[Maricela]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Amigo]]></surname>
<given-names><![CDATA[Mary-Carmen]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
</contrib-group>
<aff id="A02">
<institution><![CDATA[,INCICH Departamento de Medicina Nuclear ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,INCICH Departamento de Inmunología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A04">
<institution><![CDATA[,INCICH Departamento de Reumatología de Consulta Externa ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A01">
<institution><![CDATA[,Instituto Nacional de Cardiología Ignacio Chávez  ]]></institution>
<addr-line><![CDATA[México D.F.]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>03</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>03</month>
<year>2005</year>
</pub-date>
<volume>75</volume>
<numero>1</numero>
<fpage>42</fpage>
<lpage>48</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-99402005000100007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-99402005000100007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-99402005000100007&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Actualmente, 1 de cada 3 hombres y 1 de cada 10 mujeres desarrolla un evento cardiovascular ateroesclerótico mayor antes de los 60 años, por lo que la enfermedad arterial coronaria continúa siendo un problema de salud pública. Existe una asociación significativa entre enfermedades autoinmunes tales como lupus eritematoso sistémico, artritis reumatoide y ateroesclerosis coronaria prematura o acelerada. Los objetivos del estudio fueron: a) Valorar la perfusión miocárdica en pacientes con enfermedades reumatológicas, mediante ecocardiografia de contraste (EC) y establecer su utilidad comparando con los resultados obtenidos por medicina nuclear como método de referencia (MN). b) Evaluar la prevalencia de alteraciones en la perfusión miocárdica subclínica en enfermedades autoinmunes y establecer una estrategia para evaluar los cambios cardiovasculares en este padecimiento. Se estudiaron mediante EC en reposo y en el pico máximo del estrés y MN a 37 pacientes pertenecientes a la Consulta externa del Departamento de Reumatología para valorar la perfusión miocárdica del ventrículo izquierdo. La prevalencia de alteraciones en la perfusión miocárdica en síndrome antifosfolípido primario (SAFP), lupus eritematoso y artritis reumatoide por EC y MN, cuando estos métodos se analizaron en forma independiente o juntos fue del 27%. El valor predictivo positivo de ambas pruebas fue del 80%, la sensibilidad del 80% y la especificidad del 93%. En los pacientes con SAFP se encontró que cuando se realizan ambas pruebas diagnósticas la MN alcanza una sensibilidad del 100% si el EC es positivo y una especificidad del 100% cuando el EC negativo. Podemos concluir que es importante determinar la existencia de enfermedad coronaria subclínica en los pacientes con enfermedades inmunológicas mediante estudios no invasivos (Sestamibi SPECT y/o ecocardiografía de contraste) que permiten valorar la perfusión miocárdica.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[A significant correlation between autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and premature or accelerated coronary atherosclerosis was found. The objectives of the study were: a) evaluate myocardial perfusion in patients with rheumatic diseases by means of contrast echocardiography (CE) and to establish its usefulness as compared to the results obtained by nuclear medicine (NM) (reference method), b) evaluate the prevalence of alterations in subclinical myocardial perfusion in autoimmune diseases and to establish a strategy to evaluate the cardiovascular changes in this disease. Myocardial perfusion in 37 outpatients of the rheumatology department was evaluated by CE at rest and with pharmacological stress (dobutamine) and NM. The prevalence of alterations in the myocardial perfusion in autoimmune diseases by CE and NM, when these methods were analyzed independently or when both methods were used was 27%. The positive predictive value (PPV) and negative predictive value (NPV) of both tests was 80% and 93%, respectively, the sensitivity was 80% and the specificity was 93%. The prevalence of alterations of perfusion in the primary antiphospholipid syndrome (PAPS) was of 30%. In this patients it was found that when both diagnostic tests are performed, NM reaches a sensitivity of 100% if the CE is positive and an specificity of 100% when the CE is negative. We can conclude that it is important to determine the presence of subclinic coronary artery disease in patients with autoimmune disease by noninvasive studies such as Sestamibi SPECT and/or CE for assessment of myocardial perfusion in order to plan an adequate treatment and follow-up.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Enfermedad autoinmune]]></kwd>
<kwd lng="es"><![CDATA[Ecocardiografía de contraste]]></kwd>
<kwd lng="es"><![CDATA[Sestamibi SPECT]]></kwd>
<kwd lng="en"><![CDATA[Autoimmune disease]]></kwd>
<kwd lng="en"><![CDATA[Contrast echocardiography]]></kwd>
<kwd lng="en"><![CDATA[SPECT Sestamibi]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="4">Investigaci&oacute;n cl&iacute;nica</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="4"><b><i>An&aacute;lisis de la utilidad de ecocardiograf&iacute;a de contraste y medicina nuclear en afecci&oacute;n cardiovascular de origen autoinmune</i></b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="3"><b>Analysis of the usefulness of contrast echocardiography and nuclear medicine in cardiovascular affection due to autoimmune diseases</b></font></p>     <p align="center"><font face="verdana" size="2">&nbsp;</font></p>     <p align="center"><font face="verdana" size="2"><b>Nilda Espin&oacute;la Zavaleta,* Erick Alex&aacute;nderson ,** Mar&iacute;a Elena Soto,*** Maricela Flores,* Mary&#150;Carmen Amigo****</b></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><i>* Departamento de Ecocardiograf&iacute;a de Consulta Externa, INCICH.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i>** Departamento de Medicina Nuclear, INCICH.</i></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><i>*** Departamento de Inmunolog&iacute;a, INCICH.</i></font></p>     <p align="justify"><font face="verdana" size="2"><i>**** Departamento de Reumatolog&iacute;a de Consulta Externa, INCICH.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Correspondencia:    <br> </b><i>Nilda Espin&oacute;la Zavaleta, MD.    <br> Instituto Nacional de Cardiolog&iacute;a Ignacio Ch&aacute;vez.    <br> (INCICH, Juan Badiano No. 1, Col. Secci&oacute;n XVI, Tlalpan 14080 M&eacute;xico, D.F.). Tel&eacute;fono: 55732911 ext 1196.    <br> E&#150;mail: <a href="mailto:niesza2001@hotmail.com">niesza2001@hotmail.com</a></i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2">Recibido: 27 de enero de 2005    ]]></body>
<body><![CDATA[<br> Aceptado: 3 de febrero de 2005</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resumen</b></font></p>     <p align="justify"><font face="verdana" size="2">Actualmente, 1 de cada 3 hombres y 1 de cada 10 mujeres desarrolla un evento cardiovascular ateroescler&oacute;tico mayor antes de los 60 a&ntilde;os, por lo que la enfermedad arterial coronaria contin&uacute;a siendo un problema de salud p&uacute;blica. Existe una asociaci&oacute;n significativa entre enfermedades autoinmunes tales como lupus eritematoso sist&eacute;mico, artritis reumatoide y ateroesclerosis coronaria prematura o acelerada. Los objetivos del estudio fueron: a) Valorar la perfusi&oacute;n mioc&aacute;rdica en pacientes con enfermedades reumatol&oacute;gicas, mediante ecocardiografia de contraste (EC) y establecer su utilidad comparando con los resultados obtenidos por medicina nuclear como m&eacute;todo de referencia (MN). b) Evaluar la prevalencia de alteraciones en la perfusi&oacute;n mioc&aacute;rdica subcl&iacute;nica en enfermedades autoinmunes y establecer una estrategia para evaluar los cambios cardiovasculares en este padecimiento. Se estudiaron mediante EC en reposo y en el pico m&aacute;ximo del estr&eacute;s y MN a 37 pacientes pertenecientes a la Consulta externa del Departamento de Reumatolog&iacute;a para valorar la perfusi&oacute;n mioc&aacute;rdica del ventr&iacute;culo izquierdo. La prevalencia de alteraciones en la perfusi&oacute;n mioc&aacute;rdica en s&iacute;ndrome antifosfol&iacute;pido primario (SAFP), lupus eritematoso y artritis reumatoide por EC y MN, cuando estos m&eacute;todos se analizaron en forma independiente o juntos fue del 27%. El valor predictivo positivo de ambas pruebas fue del 80%, la sensibilidad del 80% y la especificidad del 93%. En los pacientes con SAFP se encontr&oacute; que cuando se realizan ambas pruebas diagn&oacute;sticas la MN alcanza una sensibilidad del 100% si el EC es positivo y una especificidad del 100% cuando el EC negativo. Podemos concluir que es importante determinar la existencia de enfermedad coronaria subcl&iacute;nica en los pacientes con enfermedades inmunol&oacute;gicas mediante estudios no invasivos (Sestamibi SPECT y/o ecocardiograf&iacute;a de contraste) que permiten valorar la perfusi&oacute;n mioc&aacute;rdica.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Palabras clave: </b>Enfermedad autoinmune. Ecocardiograf&iacute;a de contraste. Sestamibi SPECT.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Summary</b></font></p>     <p align="justify"><font face="verdana" size="2">A significant correlation between autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and premature or accelerated coronary atherosclerosis was found. The objectives of the study were: a) evaluate myocardial perfusion in patients with rheumatic diseases by means of contrast echocardiography (CE) and to establish its usefulness as compared to the results obtained by nuclear medicine (NM) (reference method), b) evaluate the prevalence of alterations in subclinical myocardial perfusion in autoimmune diseases and to establish a strategy to evaluate the cardiovascular changes in this disease. Myocardial perfusion in 37 outpatients of the rheumatology department was evaluated by CE at rest and with pharmacological stress (dobutamine) and NM. The prevalence of alterations in the myocardial perfusion in autoimmune diseases by CE and NM, when these methods were analyzed independently or when both methods were used was 27%. The positive predictive value (PPV) and negative predictive value (NPV) of both tests was 80% and 93%, respectively, the sensitivity was 80% and the specificity was 93%. The prevalence of alterations of perfusion in the primary antiphospholipid syndrome (PAPS) was of 30%. In this patients it was found that when both diagnostic tests are performed, NM reaches a sensitivity of 100% if the CE is positive and an specificity of 100% when the CE is negative. We can conclude that it is important to determine the presence of subclinic coronary artery disease in patients with autoimmune disease by noninvasive studies such as Sestamibi SPECT and/or CE for assessment of myocardial perfusion in order to plan an adequate treatment and follow&#150;up.</font></p>     <p align="justify"><font face="verdana" size="2"><b>Keywords: </b>Autoimmune disease. Contrast echocardiography. SPECT Sestamibi.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Introducci&oacute;n</b></font></p>     <p align="justify"><font face="verdana" size="2">En Estados Unidos, aproximadamente 900,000 personas sufren un infarto mioc&aacute;rdico cada a&ntilde;o y 350,000 mueren como resultado de complicaciones agudas y cr&oacute;nicas de enfermedad arterial coronaria, siendo &eacute;sta la principal causa de morbilidad y mortalidad. Actualmente, 1 de cada 3 hombres y 1 de cada 10 mujeres desarrolla un evento cardiovascular ateroescler&oacute;tico mayor antes de los 60 a&ntilde;os, por lo que la enfermedad arterial coronaria contin&uacute;a siendo un problema de salud p&uacute;blica.<sup>1&#150;6</sup></font></p>     <p align="justify"><font face="verdana" size="2">Existe una asociaci&oacute;n significativa entre enfermedades autoinmunes tales como lupus eritematoso sist&eacute;mico, artritis reumatoide y ateroesclerosis coronaria prematura o acelerada.<sup>7,8</sup> Eventos tromboemb&oacute;licos vasculares perif&eacute;ricos, coronarios y cerebrales son la mayor causa de morbilidad y mortalidad en pacientes con LES. Factores implicados en ateroesclerosis prematura y arteritis oclusiva incluyen da&ntilde;o endotelial mediado por inmunidad, hipertensi&oacute;n arterial sist&eacute;mica, hiperlipidemia, obesidad m&oacute;rbida, duraci&oacute;n de terapia conglucocorticoides, espasmo arterial coronario, hipercoagulabilidad relacionada a anticuerpos anticardiolipina, y niveles plasm&aacute;ticos elevados de homociste&iacute;na.<sup>9&#150;16</sup></font></p>     <p align="justify"><font face="verdana" size="2">Las pruebas cl&iacute;nicas rutinariamente disponibles usadas para detectar enfermedad ateromatosa temprana son frecuentemente invasivas (angiograf&iacute;a coronaria) o poco confiables en este grupo de pacientes (mujeres j&oacute;venes), quienes frecuentemente tienen otras anormalidades m&uacute;sculo&#150;esquel&eacute;ticas o cardiopulmonares, lo que puede limitar la precisi&oacute;n de la prueba.<sup>17,18</sup></font></p>     <p align="justify"><font face="verdana" size="2">En la actualidad se han desarrollado nuevas t&eacute;cnicas para la detecci&oacute;n de enfermedad ateroescler&oacute;tica subcl&iacute;nica como la ecocardiograf&iacute;a de contraste, que permite valorar la microcirculaci&oacute;n coronaria.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Objetivo</b></font></p>     <p align="justify"><font face="verdana" size="2">Los objetivos del estudio fueron:</font></p>     <p align="justify"><font face="verdana" size="2">Valorar la perfusi&oacute;n mioc&aacute;rdica en pacientes con enfermedades reumatol&oacute;gicas, mediante ecocardiograf&iacute;a de contraste y establecer su utilidad comparando con los resultados obtenidos por medicina nuclear (m&eacute;todo de referencia).</font></p>     <p align="justify"><font face="verdana" size="2">Evaluar la prevalencia de alteraciones en la perfusi&oacute;n mioc&aacute;rdica subcl&iacute;nica en enfermedades autoinmunes y establecer una estrategia para evaluar los cambios cardiovasculares en este padecimiento.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Pacientes y m&eacute;todos</b></font></p>     <p align="justify"><font face="verdana" size="2">Se estudiaron 37 pacientes pertenecientes a la Consulta externa del Departamento de Reumatolog&iacute;a del Instituto Nacional de Cardiolog&iacute;a "Ignacio Ch&aacute;vez", con edades comprendidas entre 18&#150;59 a&ntilde;os, que cumpl&iacute;an con los criterios diagn&oacute;sticos establecidos por la ACR para artritis reumatoide<sup>19</sup>y LES,<sup>20</sup> as&iacute; como los criterios de Sapporo para SAF primario.<sup>21</sup> Todos los pacientes incluidos firmaron hoja de consentimiento informado.</font></p>     <p align="justify"><font face="verdana" size="2">Se excluyeron mujeres embarazadas o lactantes, con enfermedad valvular severa, hipertensi&oacute;n arterial no controlada, angina inestable, o trastornos importantes del ritmo como fibrilaci&oacute;n atrial. Se eliminaron los pacientes que no tuvieron completos los estudios con los 2 m&eacute;todos diagn&oacute;sticos.</font></p>     <p align="justify"><font face="verdana" size="2">Los pacientes fueron evaluados cl&iacute;nicamente registrando sus factores de riesgo cardiovascular. Se evalu&oacute; la presencia de isquemia mioc&aacute;rdica mediante dos m&eacute;todos:</font></p>     <blockquote>       <p align="justify"><font face="verdana" size="2">1. Ecocardiograf&iacute;a con medio de contraste en reposo y con estr&eacute;s farmacol&oacute;gico (dobutamina).<sup>22</sup><sup>&#150;25</sup></font></p>       <p align="justify"><font face="verdana" size="2">2. Centelleograf&iacute;a con radion&uacute;clidos.</font></p> </blockquote>     <p align="justify"><font face="verdana" size="2">El estudio ecocardiogr&aacute;fico con dobutamina se realiz&oacute; con un equipo Philips Sonos 5500 provisto de un programa de estr&eacute;s digitalizado. La dobutamina se administr&oacute; en infusi&oacute;n, iniciando con dosis de 5 <i>&micro;</i>g/kg/min con incrementos progresivos cada 3 minutos hasta 40 <i>&micro;</i>g/kg/min. Cuando no se logr&oacute; alcanzar el 85% de la frecuencia m&aacute;xima esperada para la edad del paciente, se administr&oacute; atropina intravenosa a dosis de 0.5 mg hasta una dosis total de 2.0 mg. Las im&aacute;genes se tomaron en un formato de 4 y &eacute;stas incluyeron los ejes largo y corto parasternal y apical de 4 y 2 c&aacute;maras en condiciones b&aacute;sales, dosis bajas (5 <i>&micro;</i>g/kg/min), dosis intermedias (20 <i>&micro;</i>g/kg/min) y dosis m&aacute;ximas (40 <i>&micro;</i>g/kg/ miny atropina). La segmentaci&oacute;n del ventr&iacute;culo izquierdo se hizo de acuerdo a la establecida por la Sociedad Americana de Ecocardiograf&iacute;a (16 segmentos).<sup>26</sup></font></p>     <p align="justify"><font face="verdana" size="2">El contraste (optison) se administr&oacute; en forma intravenosa, en condiciones b&aacute;sales y en el pico m&aacute;ximo del estr&eacute;s farmacol&oacute;gico, previa activaci&oacute;n de las arm&oacute;nicas de perfusi&oacute;n y el Doppler angio. Se utiliz&oacute; 1.2 ml de Optison por paciente y cada dosis fue de 0.3 ml en bolo e inmediatamente despu&eacute;s 5 a 10 ml de soluci&oacute;n salina o glucosada en 1 minuto. Se utiliz&oacute; el eje apical de 4 y 2 c&aacute;maras y los disparos fueron 1:1, 1:3 y 1:5. El miocardio se consider&oacute; bien perfundido cuando se observ&oacute; una distribuci&oacute;n homog&eacute;nea de las microburbujas. La ausencia de contraste en una determinada zona se denomin&oacute; defecto de perfusi&oacute;n.</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Para el estudio de perfusi&oacute;n mioc&aacute;rdica con radion&uacute;clidos se utiliz&oacute; el protocolo &lt;&lt;reposo&#150;esfuerzo en un d&iacute;a&gt;&gt;, con tecnecio <sup>99m</sup> &#150; Hexakis 2&#150; metoxi2&#150;isobutil isonitrilo (Sesta MIBI), el cual es un agente que pertenece a la familia de los isonitrilos. El Sesta MIBI posee energ&iacute;a ideal para tomar im&aacute;genes con la c&aacute;mara de 140 KeV y tiene una vida media de 6 horas. Se utilizaron 8&#150;10 mCi en reposo y de 22 a 30 mCi en esfuerzo (3 veces la dosis en reposo). La dosis de esfuerzo se inyect&oacute; en el pico m&aacute;ximo. El ejercicio se continu&oacute; por lo menos un minuto m&aacute;s despu&eacute;s de la inyecci&oacute;n. La adquisici&oacute;n de las im&aacute;genes se efectu&oacute; 30 a 60 minutos despu&eacute;s de la inyecci&oacute;n. El estudio ecocardiogr&aacute;fico se consider&oacute; positivo, cuando se observ&oacute; alg&uacute;n defecto de perfusi&oacute;n ya sea en reposo, o en esfuerzo m&aacute;ximo. El estudio con radion&uacute;clidos se consider&oacute; positivo cuando se visualizaron defectos de perfusi&oacute;n en reposo o en esfuerzo m&aacute;ximo <i><a href="/img/revistas/acm/v75n1/a7f1.jpg" target="_blank">(Fig. 1)</a>.</i></font></p>     <p align="justify"><font face="verdana" size="2">Los estudios ecocardiogr&aacute;ficos y gammagr&aacute;ficos fueron realizados por un solo operador. Tanto los investigadores del servicio de ecocardiograf&iacute;a como los del servicio de medicina nuclear desconoc&iacute;an los resultados de los diferentes m&eacute;todos.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>An&aacute;lisis estad&iacute;stico</b></font></p>     <p align="justify"><font face="verdana" size="2">Las variables param&eacute;tricas se expresaron en medias y desviaci&oacute;n est&aacute;ndar, y las variables no param&eacute;tricas en frecuencias y porcentajes. Se evalu&oacute; en ambos estudios el valor predictivo positivo, el valor predictivo negativo, la sensibilidad y la especificidad y an&aacute;lisis para utilidad por pruebas diagn&oacute;sticas; se realiz&oacute; tambi&eacute;n &aacute;rbol de decisiones. Los resultados de ambas pruebas se expresaron en tablas de 2 x 2, consider&aacute;ndose como est&aacute;ndar de oro, el resultado del estudio con radion&uacute;clidos.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Resultados</b></font></p>     <p align="justify"><font face="verdana" size="2">De los 37 pacientes estudiados, el 81% pertenec&iacute;a al g&eacute;nero femenino, con una edad media de 35.5 &plusmn; 9.9 a&ntilde;os (18&#150;59). La edad media de los hombres fue de 33.43 &plusmn; 10.97 (21&#150;51) y de las mujeres de 36.07 &plusmn; 9.77 (18&#150;59). El 38% de los pacientes ten&iacute;an AR, 32% padec&iacute;an LES y el 30% SAF primario. </font></p>     <p align="justify"><font face="verdana" size="2">El tiempo de evoluci&oacute;n desde su diagn&oacute;stico fue de 6.4 &plusmn; 5.2 a&ntilde;os en promedio.</font></p>     <p align="justify"><font face="verdana" size="2">Los niveles de colesterol total fueron de 162 &plusmn; 39.8 mg/dl y los de triglic&eacute;ridos de 128.9 &plusmn; 58.1 <i>mg/dl <a href="/img/revistas/acm/v75n1/a7t1.jpg" target="_blank">(Tabla I)</a>.</i></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Alteraciones en la perfusi&oacute;n</b></font></p>     <p align="justify"><font face="verdana" size="2">La prevalencia de alteraciones en la perfusi&oacute;n mioc&aacute;rdica en S AFP, lupus y artritis reumatoide por ecocardiograf&iacute;a de contraste y medicina nuclear, cuando estos m&eacute;todos se analizaron en forma independiente fue del 27% (10/37) <i><a href="/img/revistas/acm/v75n1/a7t2.jpg" target="_blank">(Tabla II)</a>. </i>Cuando los pacientes se analizan utilizando los dos m&eacute;todos, la prevalencia de las alteraciones en la perfusi&oacute;n mioc&aacute;rdica es la misma, pero el valor predictivo positivo de ambas pruebas fue del 80%, la sensibilidad del 80% y la especificidad del 93%. El cambio de probabilidad pre&#150;prueba o ganancia es de + 53%.</font></p>     <p align="justify"><font face="verdana" size="2">Cuando la prueba es positiva por ecocardiograf&iacute;a de contraste en pacientes con enfermedades inmunol&oacute;gicas tiene 10 veces la probabilidad de confirmar la presencia de alteraciones en la perfusi&oacute;n micoc&aacute;rdica y la prevalencia pre&#150;prueba es del 27% y la prevalencia post&#150;prueba es del 92%. La prevalencia de las alteraciones de la perfusi&oacute;n en el SAFP es del 30%. En este estudio se encontr&oacute; que cuando se realizan ambas pruebas diagn&oacute;sticas la medicina nuclear alcanza una sensibilidad del 100% si el ecocardiograma de contraste es positivo y una especificidad del 100% cuando el ecocardiograma de contraste es negativo. Cuando ambas pruebas diagn&oacute;sticas son positivas el valor predictivo positivo (VPP) es del 63%, lo que indica que la prevalencia pre&#150;prueba es de + 33%, en cambio cuando s&oacute;lo una prueba es positiva el VPP disminuye al 58% y la prevalencia post&#150;prueba es del 58%.</font></p>     <p align="justify"><font face="verdana" size="2">Cuando el ecocardiograma de contraste se realiza en forma independiente, la probabilidad de detectar alteraciones en la perfusi&oacute;n mioc&aacute;rdica es de 2.25 y para medicina nuclear es de 5.3 3. Cuando se realizan los dos estudios y uno o ambos son positivos, la sensibilidad es de 64% y la especificidad de 81% y si uno o ambos son negativos, la sensibilidad es de 45% y la especificidad de 88%.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Discusi&oacute;n</b></font></p>     <p align="justify"><font face="verdana" size="2">Por m&aacute;s de 20 a&ntilde;os la enfermedad coronaria prematura se ha reconocido como el mayor determinante de morbilidad y mortalidad en pacientes con LES. A pesar de la clara distinci&oacute;n en la fisiopatolog&iacute;a, la disfunci&oacute;n inmune resulta en un estado inflamatorio cr&oacute;nico, que puede tener implicaciones para la aterog&eacute;nesis en los pacientes j&oacute;venes.<sup>27</sup> Las mujeres con LES tienen alta incidencia de enfermedad coronaria. Varios investigadores han demostrado que la mujeres con LES menores de 45 a&ntilde;os tiene sustancialmente incrementado el riesgo de enfermedad coronaria. Se ha reportado que las mujeres l&uacute;picas con edades entre 35 a 44 a&ntilde;os tienen m&aacute;s de 50 veces la posibilidad de desarrollar infarto del miocardio que las mujeres controles pareadas por edad. En cambio las mujeres l&uacute;picas con edades entre 45 y 64 a&ntilde;os la posibilidad de desarrollar infarto es 2 a 4 veces mayor que el grupo control.<sup>28&#150;29 </sup>La artritis reumatoide se asocia con tasas mayores de enfermedad cardiovascular.</font></p>     <p align="justify"><font face="verdana" size="2">La tasa de mortalidad estandarizada oscila entre 1.13 a 5.25 en pacientes con AR que mueren por causas circulatorias con mayor riesgo en mujeres y la sobrevida promedio es 17 a&ntilde;os menor que la sobrevida en poblaci&oacute;n general.<sup>29&#150;31</sup> La disfunci&oacute;n endotelial es un evento temprano en la patog&eacute;nesis de la ateroesclerosis en estos pacientes. Se ha encontrado que la funci&oacute;n vascular es anormal en AR con elasticidad de las arterias de peque&ntilde;o calibre y de gran calibre disminuida e incremento de la resistencia vascular. Existe una relaci&oacute;n inversa entre la elasticidad arterial y los par&aacute;metros de inflamaci&oacute;n.<sup>32,33</sup></font></p>     <p align="justify"><font face="verdana" size="2">A pesar de que muchos factores causan ateroesclerosis, la inflamaci&oacute;n vascular es probablemente el mediador principal de la aterog&eacute;nesis en enfermedades inmunol&oacute;gicas, observaciones epidemiol&oacute;gicas han relacionado la inflamaci&oacute;n con los eventos cardiovasculares. La pro te&iacute;na C reactiva, reactante de la fase aguda frecuentemente incrementada en enfermedad autoinmune activa, ha mostrado ser un factor predictor de riesgo independiente en futuros eventos de infarto agudo al miocardio e infarto cerebral. La inflamaci&oacute;n puede tener algunos efectos procoagulantes e inductores de ateroesclerosis. Las enfermedades autoinmunes tienen un impacto m&aacute;s directo en la ateroesclerosis prematura. Los mecanismos moleculares mediadores de la interacci&oacute;n entre las enfermedades autoinmunes y el metabolismo de las HDL son desconocidos, aunque existen algunas explicaciones: Primero, el proceso inflamatorio influye frecuentemente en el nivel de las lipoprote&iacute;nas, posiblemente a trav&eacute;s de la acci&oacute;n de varias citoquinas y factores de crecimiento. Los efectos de la mutaci&oacute;n gen&eacute;tica en el metabolismo de las HDL pueden ser secundarios a la inflamaci&oacute;n que acompa&ntilde;a a las enfermedades autoinmunes.<sup>34&#150;36</sup> Estudios epidemiol&oacute;gicos han establecido que niveles elevados de LDL representan uno de los factores m&aacute;s importantes para el desarrollo de ateroesclerosis.<sup>37</sup> La LDL&#150;oxidada parece tener un papel central. Observaciones recientes han mostrado la presencia de anticuerpos anti&#150;LDL&#150;oxidada en pacientes con lupus eritematoso generalizado (LEG) y s&iacute;ndrome de anticuerpos antifosfol&iacute;pidos (SAF), lo cual puede contribuir a la ateroesclerosis acelerada que se ha observado en estos pacientes.<sup>38,39</sup></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">El diagn&oacute;stico de afecci&oacute;n card&iacute;aca en enfermedades autoinmunes es dif&iacute;cil, debido a la falta de m&eacute;todos de imagen no invasivos, ya que el 30 a 45% de los pacientes tiene enfermedad coronaria subcl&iacute;nica.<sup>27</sup> Existen pocos estudios no invasivos (SPECT) que han valorado las alteraciones de la perfusi&oacute;n mioc&aacute;rdica en enfermedades autoinmunes.<sup>40</sup><sup>&#150;42</sup> En nuestro estudio valoramos la perfusi&oacute;n mioc&aacute;rdica en pacientes con enfermedades autoinmunes, utilizando dos m&eacute;todos: Sestamibi SPECT y ecocardiograf&iacute;a de contraste. La prevalencia de alteraciones en la perfusi&oacute;n, utilizando como est&aacute;ndar de oro el estudio Sestamibi SPECT en las enfermedades inmunol&oacute;gicas: SAF, AR y LES analizada en forma independiente fue del 27%, cifra similar a la reportada en la literatura. Los niveles de colesterol total en estos pacientes se encontraron dentro de rangos normales, por lo que las alteraciones de la perfusi&oacute;n detectadas en nuestros pacientes no se pueden atribuir a ateroesclerosis coronaria, sino m&aacute;s bien a la enfermedad autoinmune con todos los mecanismos explicados previamente.</font></p>     <p align="justify"><font face="verdana" size="2">Cuando se analizaron por separado AR, LES y SAFP la utilidad principal fue en pacientes con SAFP. En los pacientes con SAFP se pudo observar que ambos m&eacute;todos son &uacute;tiles en el diagn&oacute;stico de las alteraciones de la perfusi&oacute;n mioc&aacute;rdica con una sensibilidad y especificidad del 100%, situaci&oacute;n no descrita previamente, en cambio en AR y LES no se encontraron los mismos resultados y hemos considerado que quiz&aacute;s se debe a la falta de muestra, por lo que requerir&aacute; un an&aacute;lisis a futuro con m&aacute;s pacientes.</font></p>     <p align="justify"><font face="verdana" size="2">En base a nuestros resultados elaboramos un diagrama de flujo en el cual se demuestra que la utilidad esperada al realizar un estudio de perfusi&oacute;n mioc&aacute;rdica en los pacientes con SAF, LES y AR es del 86% <i>vs </i>76% cuando &eacute;ste no se realiza <i><a href="/img/revistas/acm/v75n1/a7f2.jpg" target="_blank">(Fig. 2)</a>.</i></font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Conclusiones</b></font></p>     <p align="justify"><font face="verdana" size="2">Podemos concluir que es importante determinar la existencia de enfermedad coronaria subcl&iacute;nica en los pacientes con enfermedades inmunol&oacute;gicas mediante estudios no invasivos (Sestamibi SPECT y/o ecocardiograf&iacute;a de contraste) que permiten valorar la perfusi&oacute;n mioc&aacute;rdica. Sin embargo, consideramos que habr&aacute; que analizar otro estudio incluyendo pacientes con enfermedad inmunol&oacute;gica activa e inactiva, elegidos aleatoriamente para evaluar costos y beneficios.</font></p>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>     <p align="justify"><font face="verdana" size="2"><b>Referencias</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2">1. Ghaffari Sasan MD: <i>Detection and Management of coronary artery disease in patients with rheumatologic disorders. </i>In Rheumatic diseases Clinics of North America. 1999; 25(3): 657&#150;668.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031818&pid=S1405-9940200500010000700001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">2. French WJ: <i>Trends in Acute Myocardial Infarction Management: Use of the national registry of myocardial infarction in quality improvement. </i>Am J Cardiol 2000; 85: 5B&#150;9B.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031819&pid=S1405-9940200500010000700002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">3. Rabbani R, Topol E: <i>Strategies to achieve coronary arterial plaque stabilization. </i>Cardiovasc research 1999; 41: 402&#150;417.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031820&pid=S1405-9940200500010000700003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">4. Hamm Cristhian, Braunwald Eugene: <i>A classification of Unstable angina revisited. </i>Circulation 2000;102: 118&#150;122.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031821&pid=S1405-9940200500010000700004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">5. <i>Lusis AJ: Atherosclerosis. </i>Nature 2000; 407:233&#150;241.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031822&pid=S1405-9940200500010000700005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">6. Ross R: <i>Atherosclerosis &#150;An inflammatory disease. </i>NEJM 1999; 340(2): 115&#150;125.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031823&pid=S1405-9940200500010000700006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">7. George J, Afek A, Gilburd B, Harats D, Shoenfeld Y: <i>Autoimmunity in atherosclerosis: lessons from experimental models. </i>Lupus 2000; 9:223&#150;227.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031824&pid=S1405-9940200500010000700007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">8. De Winther M, Hofker M: <i>Scavenging new insights into atherogenesis. </i>J Clin Invest 2000; 105(8): 1039&#150;1041.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031825&pid=S1405-9940200500010000700008&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">9. Wierzbicki AS: <i>Lipids, cardiovascular disease and atherosclerosis in systemic lupus erythematosus. </i>Lupus 2000; 9: 194&#150;201.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031826&pid=S1405-9940200500010000700009&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">10. Gladman DD, Urowitz MB: <i>Morbidity in systemic lupus erythematosus. </i>J Rheumatol 1987; 14(S13): 223&#150;226.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031827&pid=S1405-9940200500010000700010&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">11. Petri M, P&eacute;rez&#150;Gutthann S, Spence D, Hochberg MC: <i>Risk factor for coronary artery disease in patients &#150;with systemic lupus erythematosus. </i>Am J Med 1992;93: 513&#150;519.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031828&pid=S1405-9940200500010000700011&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">12. Sultan H, Berson J, Mrotznik J, Ginzler EM: <i>Lack of evidence for corticosteroids as a risk factor for coronary artery disease in systemic lupus erythematosus. </i>Northeast Region American College of Rheumatology Meeting, New York, June 1994.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031829&pid=S1405-9940200500010000700012&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">13. Manzi S, Meilahn EN, Rairie JE, Cont&eacute; CG, Medsger TAQ, Jansen&#150;Mc Williams L, D'Agostino RB, Kuller LH: <i>Age&#150;specific incidence rates of myocardial infarction and angina in women with Systemic Lupus Erythematosus: Comparison with the Framingham study. </i>Am J Epidemiol 1997: 145: 408&#150;415.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031830&pid=S1405-9940200500010000700013&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">14. Badui E, Garc&iacute;a&#150;Rub&iacute; D, Robles E, Jim&eacute;nez J, Juan L, Deleze M, D&iacute;az A, Mintz G: <i>Cardiovascular manifestations in systemic lupus erythematosus; prospective study of 100 patients. </i>Angiology 1985; 36: 431&#150;441.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031831&pid=S1405-9940200500010000700014&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">15. Hosenpud JD, Montanaro A, Hart MV, Haines JE, Specht HD, Bennett RM, Kloster FE: <i>Myocardial perfusion abnormalities in asymptomatic patients with systemic lupus erythematosus. </i>Am J Med 1984; 77: 286&#150;292.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031832&pid=S1405-9940200500010000700015&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">16. Ginzler E, Stein R, Solomon N, Frank F: <i>Coronary artery disease and ventricular function in long&#150;term systemic lupus erythematosus patients. </i>American Rheumatism Association Meeting, Atlanta, May 1980.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031833&pid=S1405-9940200500010000700016&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">17. Bruce IN, Burns RJ, Gladman DD, Urowitz MB: <i>High prevalence of myocardial perfusion abnormalities in women with LES. </i>Arthritis Rheum 1997; 40: S219.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031834&pid=S1405-9940200500010000700017&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">18. Bruce IN, Burns RJ, Gladman DD, Urowitz MB: <i>Single photon emission computed tomography dual isotope myocardial perfusion imaging in women with SLE. I. Prevalence and distribution of abnormalities. </i>J Rheumatol 2000; 27: 2372&#150;2377.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031835&pid=S1405-9940200500010000700018&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">19. Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR: <i>The American Rheumatism Association 1987 Criteria. </i>Arthritis Rheum 1988;31:315&#150;328.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031836&pid=S1405-9940200500010000700019&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">20. Tan EM, Cohen AS, Fries JF, Masi AT, McShane DJ, Rothfield NF, Schaller JG, Talal N, Winhester RJ: <i>The 1982 revised criteria for the classification of systematic lupus erythematosus (SLE). </i>Arthritis Rheum 1982; 25: 1271&#150;1277.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031837&pid=S1405-9940200500010000700020&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">21. Wilson WA, Gharavi AE, Koike T, Lockshin MD, Branch DW, Piette JO, Brey R, Derksen R, Harris EN, Hughes GR, Triplett DA, Khamashta M: <i>International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome: report of an international workshop. </i>Arthritis Rheum 1999; 42(7): 1309&#150;1311.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031838&pid=S1405-9940200500010000700021&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">22. Rainbird A, Mulvagh S, Oh K, McCully R, Klarich K. <i>Contrast dobutamine stress echocardiography: Clinical practice assessment in 300 consecutive patients. </i>J Am Soc Echocardiogr 2001; 14: 378&#150;85.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031839&pid=S1405-9940200500010000700022&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">23.&nbsp; Main M, Grayburn P: <i>Clinical applications of transpulmonary contrast echocardiography. </i>Am Heart J 1999; 137(1): 144&#150;153.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031840&pid=S1405-9940200500010000700023&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">24. Porter TR, Xie F, Li S, D'Sa A, Rafter P: <i>Increased ultrasound contrast and decreased microbubble destruction rates with triggered ultrasound imaging. </i>J Am Soc Echocardiogr 1996; 9: 599&#150;605.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031841&pid=S1405-9940200500010000700024&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">25. Porter TR, Xie F, Kricsfeld D, Ambrusterbe RW: <i>Improved myocardial contrast with second harmonic transient response imaging in humans using intravenous perfluorocarbon&#150;exposed sonicated dextrose albumin. </i>J Am Coll Cardiol 1996; 27: 1496&#150;501.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031842&pid=S1405-9940200500010000700025&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">26. Crouse L, Kramer P: <i>Stress echocardiography: Technical considerations. </i>Progress cardiovasc dis 2001; 43(4): 303&#150;314.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031843&pid=S1405-9940200500010000700026&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">27. Moder KG, Miller TD, Tazelaar HD: <i>Cardiac involvement in systemic lupus erythematosus. </i>Mayo Clin Proc 1999; 74: 275&#150;284.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031844&pid=S1405-9940200500010000700027&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">28. Ward MM: <i>Premature morbidity from cardiovascular and cerebrovascular diseases in women with systemic lupus erythematosus. </i>Arthritis Rheum 1999; 42: 338&#150;346.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031845&pid=S1405-9940200500010000700028&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">29. Manzi S, Wasko M&#150;C: <i>Inflammation&#150;mediated rheumatic diseases and atherosclerosis. </i>Ann Rheum Dis 2000; 59: 321&#150;325.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031846&pid=S1405-9940200500010000700029&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">30. Cisternas M, Gutierrrez MA, Klaassen J, Acosta AM, Jacobelli S: <i>Cardiovascular risk factors in Chilean patients with rheumatoid arthritis. </i>J Rheumatol 2002; 29: 1619&#150;1622.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031847&pid=S1405-9940200500010000700030&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">31. Mutru O, Laakso M, Isomaki H, Koota K: <i>Cardiovascular mortality in patients with rheumatoid arthritis. </i>Cardiology 1989; 76: 71&#150;77.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031848&pid=S1405-9940200500010000700031&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">32. Cohn JN: <i>Arterial compliance to stratify cardiovascular risk more precision in therapeutic decision making. </i>Am J Hypertens 2001; 14: 258S&#150;63S.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031849&pid=S1405-9940200500010000700032&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">33. Wong M, Toh L, Wilson A, Roeley K, Karschimkus C, Prior D, Romas E, Clemens L, Dragicevic G, Harianto H, Wicks I, Best J, Jenkins A: <i>Reduced arterial elasticity in rheumatoid arthritis and the relationship to vascular disease risk factors and inflammation. </i>Arthritis and Rheum 2003; 48: 81&#150;89.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031850&pid=S1405-9940200500010000700033&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">34. Motoyoshi K, Takaku F: <i>Serum cholesterol&#150;lowering activity of human monocytic colony&#150;stimulating factor. </i>Lancet 1989; 2: 326&#150;327.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031851&pid=S1405-9940200500010000700034&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">35. De Viliers WJ, Farser IP, Hughes DA, Doyle AG, Gordon S: <i>Macrophage&#150;colony&#150;stimulating factor selectively enhances macrophage scavenger receptor expression and function. </i>J Exp Med 1994; 180: 705&#150;709.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031852&pid=S1405-9940200500010000700035&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">36. Horkko S, Miller E, Dudl E, Reaven P, Curtiss LK, Zvaifler Nj, Terkeltaub R, Pierangeli SS, Branch DW, Palinski W, Witztum JL: <i>Antiphospholipid antibodies are directed against epitopes of oxidized phospholipids: recognition of cardiolipin by monoclonal antibodies to epitopes of oxidized low density lipoprotein. </i>J Clin Invest 1996; 98: 815&#150;825.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031853&pid=S1405-9940200500010000700036&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">37. Libby P: The pathogenesis of atherosclerosis. In: Kasper DL, Ed. <i>Harrison's Principles of Internal Medicine. </i>16<sup>th</sup> ed. United States of America, 2005. pp. 1425&#150;1430.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031854&pid=S1405-9940200500010000700037&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">38. Amengual O, Atsumi T, Khamashta MA, Tinahones F, Hughes GRV: <i>Antibodies against oxidized low&#150;density lipoprotein in antiphospholipid syndrome. </i>Br J Rheumatol 1997; 36: 964&#150;968.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031855&pid=S1405-9940200500010000700038&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">39. Vaarala O, Alfthan G, Jauhiainen M, Leirsalo&#150;Repo M, Aho K, Palosuo T: <i>Crossreaction between antibodies to oxidized lipoprotein and to cardiolipin in systemic lupus erythematosus. </i>Lancet 1993; 341: 923&#150;925.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031856&pid=S1405-9940200500010000700039&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">40. Bruce IN, Gladman DD, Iba&ntilde;ez D, Urowitz MB: <i>Single photon emission computed tomography dual isotope myocardial perfusion imaging in women with systemic lupus erythematosus. II. Predictive factors for perfusion abnormalities. </i>J Rheumatol 2003; 30: 288&#150;291.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031857&pid=S1405-9940200500010000700040&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">41. <i>Lin JJ, Hsu HB, Sun SS, Wang JJ, Ho ST, Kao CH. Single photon emission computed tomography of technetium&#150;99m tetrofosmin myocardial perfusion imaging in patients with systemic lupus erythematosus&#150; A preliminary report. </i>Jpn Heart J 2003; 44: 83&#150;89.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031858&pid=S1405-9940200500010000700041&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p align="justify"><font face="verdana" size="2">42. Schillaci O, Laga&ntilde;a B, Danieli R, Gentile R, Tubani L, Baratta L, Scopinaro F: <i>Technetium&#150;99m Sestamibi single&#150;photon emission tomography detects subclinical myocardial perfusion abnormalities in patients with systemic lupus erythematosus. </i>Eur J Nucl Med 1999; 26: 713&#150;717.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1031859&pid=S1405-9940200500010000700042&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ghaffari Sasan]]></surname>
<given-names><![CDATA[MD]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Detection and Management of coronary artery disease in patients with rheumatologic disorders]]></article-title>
<source><![CDATA[Rheumatic diseases Clinics of North America]]></source>
<year>1999</year>
<volume>25</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>657-668</page-range></nlm-citation>
</ref>
<ref id="B2">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[French]]></surname>
<given-names><![CDATA[WJ]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Trends in Acute Myocardial Infarction Management: Use of the national registry of myocardial infarction in quality improvement]]></article-title>
<source><![CDATA[Am J Cardiol]]></source>
<year>2000</year>
<numero>85</numero>
<issue>85</issue>
<page-range>5B-9B</page-range></nlm-citation>
</ref>
<ref id="B3">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rabbani]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Topol]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Strategies to achieve coronary arterial plaque stabilization]]></article-title>
<source><![CDATA[Cardiovasc research]]></source>
<year>1999</year>
<numero>41</numero>
<issue>41</issue>
<page-range>402-417</page-range></nlm-citation>
</ref>
<ref id="B4">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hamm]]></surname>
<given-names><![CDATA[Cristhian]]></given-names>
</name>
<name>
<surname><![CDATA[Braunwald]]></surname>
<given-names><![CDATA[Eugene]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[A classification of Unstable angina revisited]]></article-title>
<source><![CDATA[Circulation]]></source>
<year>2000</year>
<numero>102</numero>
<issue>102</issue>
<page-range>118-122</page-range></nlm-citation>
</ref>
<ref id="B5">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Lusis]]></surname>
<given-names><![CDATA[AJ]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Atherosclerosis]]></article-title>
<source><![CDATA[Nature]]></source>
<year>2000</year>
<numero>407</numero>
<issue>407</issue>
<page-range>233-241</page-range></nlm-citation>
</ref>
<ref id="B6">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ross]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Atherosclerosis: An inflammatory disease]]></article-title>
<source><![CDATA[NEJM]]></source>
<year>1999</year>
<volume>340</volume>
<numero>2</numero>
<issue>2</issue>
<page-range>115-125</page-range></nlm-citation>
</ref>
<ref id="B7">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[George]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Afek]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Gilburd]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Harats]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Shoenfeld]]></surname>
<given-names><![CDATA[Y]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Autoimmunity in atherosclerosis: lessons from experimental models]]></article-title>
<source><![CDATA[Lupus]]></source>
<year>2000</year>
<numero>9</numero>
<issue>9</issue>
<page-range>223-227</page-range></nlm-citation>
</ref>
<ref id="B8">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[De Winther]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Hofker]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Scavenging new insights into atherogenesis]]></article-title>
<source><![CDATA[J Clin Invest]]></source>
<year>2000</year>
<volume>105</volume>
<numero>8</numero>
<issue>8</issue>
<page-range>1039-1041</page-range></nlm-citation>
</ref>
<ref id="B9">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wierzbicki]]></surname>
<given-names><![CDATA[AS]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Lipids, cardiovascular disease and atherosclerosis in systemic lupus erythematosus]]></article-title>
<source><![CDATA[Lupus]]></source>
<year>2000</year>
<numero>9</numero>
<issue>9</issue>
<page-range>194-201</page-range></nlm-citation>
</ref>
<ref id="B10">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Gladman]]></surname>
<given-names><![CDATA[DD]]></given-names>
</name>
<name>
<surname><![CDATA[Urowitz]]></surname>
<given-names><![CDATA[MB]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Morbidity in systemic lupus erythematosus]]></article-title>
<source><![CDATA[J Rheumatol]]></source>
<year>1987</year>
<volume>14</volume>
<numero>^sS13</numero>
<issue>^sS13</issue>
<supplement>S13</supplement>
<page-range>223-226</page-range></nlm-citation>
</ref>
<ref id="B11">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Petri]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Pérez-Gutthann]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Spence]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Hochberg]]></surname>
<given-names><![CDATA[MC]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Risk factor for coronary artery disease in patients -with systemic lupus erythematosus]]></article-title>
<source><![CDATA[Am J Med]]></source>
<year>1992</year>
<numero>93</numero>
<issue>93</issue>
<page-range>513-519</page-range></nlm-citation>
</ref>
<ref id="B12">
<nlm-citation citation-type="confpro">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Sultan]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Berson]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Mrotznik]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Ginzler]]></surname>
<given-names><![CDATA[EM]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Lack of evidence for corticosteroids as a risk factor for coronary artery disease in systemic lupus erythematosus]]></article-title>
<source><![CDATA[]]></source>
<year></year>
<conf-name><![CDATA[ Northeast Region American College of Rheumatology Meeting]]></conf-name>
<conf-date>June 1994</conf-date>
<conf-loc>New York </conf-loc>
</nlm-citation>
</ref>
<ref id="B13">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Manzi]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Meilahn]]></surname>
<given-names><![CDATA[EN]]></given-names>
</name>
<name>
<surname><![CDATA[Rairie]]></surname>
<given-names><![CDATA[JE]]></given-names>
</name>
<name>
<surname><![CDATA[Conté]]></surname>
<given-names><![CDATA[CG]]></given-names>
</name>
<name>
<surname><![CDATA[Medsger]]></surname>
<given-names><![CDATA[TAQ]]></given-names>
</name>
<name>
<surname><![CDATA[Jansen-Mc Williams]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[D'Agostino]]></surname>
<given-names><![CDATA[RB]]></given-names>
</name>
<name>
<surname><![CDATA[Kuller]]></surname>
<given-names><![CDATA[LH]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Age-specific incidence rates of myocardial infarction and angina in women with Systemic Lupus Erythematosus: Comparison with the Framingham study]]></article-title>
<source><![CDATA[Am J Epidemiol]]></source>
<year>1997</year>
<numero>145</numero>
<issue>145</issue>
<page-range>408-415</page-range></nlm-citation>
</ref>
<ref id="B14">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Badui]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[García-Rubí]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Robles]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Jiménez]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Juan]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Deleze]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Díaz]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Mintz]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cardiovascular manifestations in systemic lupus erythematosus: prospective study of 100 patients]]></article-title>
<source><![CDATA[Angiology]]></source>
<year>1985</year>
<numero>36</numero>
<issue>36</issue>
<page-range>431-441</page-range></nlm-citation>
</ref>
<ref id="B15">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hosenpud]]></surname>
<given-names><![CDATA[JD]]></given-names>
</name>
<name>
<surname><![CDATA[Montanaro]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Hart]]></surname>
<given-names><![CDATA[MV]]></given-names>
</name>
<name>
<surname><![CDATA[Haines]]></surname>
<given-names><![CDATA[JE]]></given-names>
</name>
<name>
<surname><![CDATA[Specht]]></surname>
<given-names><![CDATA[HD]]></given-names>
</name>
<name>
<surname><![CDATA[Bennett]]></surname>
<given-names><![CDATA[RM]]></given-names>
</name>
<name>
<surname><![CDATA[Kloster]]></surname>
<given-names><![CDATA[FE]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Myocardial perfusion abnormalities in asymptomatic patients with systemic lupus erythematosus]]></article-title>
<source><![CDATA[Am J Med]]></source>
<year>1984</year>
<numero>77</numero>
<issue>77</issue>
<page-range>286-292</page-range></nlm-citation>
</ref>
<ref id="B16">
<nlm-citation citation-type="confpro">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ginzler]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Stein]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Solomon]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Frank]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Coronary artery disease and ventricular function in long-term systemic lupus erythematosus patients]]></article-title>
<source><![CDATA[]]></source>
<year></year>
<conf-name><![CDATA[ American Rheumatism Association Meeting]]></conf-name>
<conf-date>May 1980</conf-date>
<conf-loc>Atlanta </conf-loc>
</nlm-citation>
</ref>
<ref id="B17">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bruce]]></surname>
<given-names><![CDATA[IN]]></given-names>
</name>
<name>
<surname><![CDATA[Burns]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
<name>
<surname><![CDATA[Gladman]]></surname>
<given-names><![CDATA[DD]]></given-names>
</name>
<name>
<surname><![CDATA[Urowitz]]></surname>
<given-names><![CDATA[MB]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[High prevalence of myocardial perfusion abnormalities in women with LES]]></article-title>
<source><![CDATA[Arthritis Rheum]]></source>
<year>1997</year>
<numero>40</numero>
<issue>40</issue>
<page-range>S219</page-range></nlm-citation>
</ref>
<ref id="B18">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bruce]]></surname>
<given-names><![CDATA[IN]]></given-names>
</name>
<name>
<surname><![CDATA[Burns]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
<name>
<surname><![CDATA[Gladman]]></surname>
<given-names><![CDATA[DD]]></given-names>
</name>
<name>
<surname><![CDATA[Urowitz]]></surname>
<given-names><![CDATA[MB]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Single photon emission computed tomography dual isotope myocardial perfusion imaging in women with SLE.: I. Prevalence and distribution of abnormalities]]></article-title>
<source><![CDATA[J Rheumatol]]></source>
<year>2000</year>
<numero>27</numero>
<issue>27</issue>
<page-range>2372-2377</page-range></nlm-citation>
</ref>
<ref id="B19">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Arnett]]></surname>
<given-names><![CDATA[FC]]></given-names>
</name>
<name>
<surname><![CDATA[Edworthy]]></surname>
<given-names><![CDATA[SM]]></given-names>
</name>
<name>
<surname><![CDATA[Bloch]]></surname>
<given-names><![CDATA[DA]]></given-names>
</name>
<name>
<surname><![CDATA[McShane]]></surname>
<given-names><![CDATA[DJ]]></given-names>
</name>
<name>
<surname><![CDATA[Fries]]></surname>
<given-names><![CDATA[JF]]></given-names>
</name>
<name>
<surname><![CDATA[Cooper]]></surname>
<given-names><![CDATA[NS]]></given-names>
</name>
<name>
<surname><![CDATA[Healey]]></surname>
<given-names><![CDATA[LA]]></given-names>
</name>
<name>
<surname><![CDATA[Kaplan]]></surname>
<given-names><![CDATA[SR]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The American Rheumatism Association 1987 Criteria]]></article-title>
<source><![CDATA[Arthritis Rheum]]></source>
<year>1988</year>
<numero>31</numero>
<issue>31</issue>
<page-range>315-328</page-range></nlm-citation>
</ref>
<ref id="B20">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Tan]]></surname>
<given-names><![CDATA[EM]]></given-names>
</name>
<name>
<surname><![CDATA[Cohen]]></surname>
<given-names><![CDATA[AS]]></given-names>
</name>
<name>
<surname><![CDATA[Fries]]></surname>
<given-names><![CDATA[JF]]></given-names>
</name>
<name>
<surname><![CDATA[Masi]]></surname>
<given-names><![CDATA[AT]]></given-names>
</name>
<name>
<surname><![CDATA[McShane]]></surname>
<given-names><![CDATA[DJ]]></given-names>
</name>
<name>
<surname><![CDATA[Rothfield]]></surname>
<given-names><![CDATA[NF]]></given-names>
</name>
<name>
<surname><![CDATA[Schaller]]></surname>
<given-names><![CDATA[JG]]></given-names>
</name>
<name>
<surname><![CDATA[Talal]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Winhester]]></surname>
<given-names><![CDATA[RJ]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The 1982 revised criteria for the classification of systematic lupus erythematosus (SLE)]]></article-title>
<source><![CDATA[Arthritis Rheum]]></source>
<year>1982</year>
<numero>25</numero>
<issue>25</issue>
<page-range>1271-1277</page-range></nlm-citation>
</ref>
<ref id="B21">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wilson]]></surname>
<given-names><![CDATA[WA]]></given-names>
</name>
<name>
<surname><![CDATA[Gharavi]]></surname>
<given-names><![CDATA[AE]]></given-names>
</name>
<name>
<surname><![CDATA[Koike]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Lockshin]]></surname>
<given-names><![CDATA[MD]]></given-names>
</name>
<name>
<surname><![CDATA[Branch]]></surname>
<given-names><![CDATA[DW]]></given-names>
</name>
<name>
<surname><![CDATA[Piette]]></surname>
<given-names><![CDATA[JO]]></given-names>
</name>
<name>
<surname><![CDATA[Brey]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Derksen]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Harris]]></surname>
<given-names><![CDATA[EN]]></given-names>
</name>
<name>
<surname><![CDATA[Hughes]]></surname>
<given-names><![CDATA[GR]]></given-names>
</name>
<name>
<surname><![CDATA[Triplett]]></surname>
<given-names><![CDATA[DA]]></given-names>
</name>
<name>
<surname><![CDATA[Khamashta]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome: report of an international workshop]]></article-title>
<source><![CDATA[Arthritis Rheum]]></source>
<year>1999</year>
<volume>42</volume>
<numero>7</numero>
<issue>7</issue>
<page-range>1309-1311</page-range></nlm-citation>
</ref>
<ref id="B22">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Rainbird]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Mulvagh]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Oh]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[McCully]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Klarich]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Contrast dobutamine stress echocardiography: Clinical practice assessment in 300 consecutive patients]]></article-title>
<source><![CDATA[J Am Soc Echocardiogr]]></source>
<year>2001</year>
<numero>14</numero>
<issue>14</issue>
<page-range>378-85</page-range></nlm-citation>
</ref>
<ref id="B23">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Main]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Grayburn]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Clinical applications of transpulmonary contrast echocardiography]]></article-title>
<source><![CDATA[Am Heart J]]></source>
<year>1999</year>
<volume>137</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>144-153</page-range></nlm-citation>
</ref>
<ref id="B24">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Porter]]></surname>
<given-names><![CDATA[TR]]></given-names>
</name>
<name>
<surname><![CDATA[Xie]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Li]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[D'Sa]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Rafter]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Increased ultrasound contrast and decreased microbubble destruction rates with triggered ultrasound imaging]]></article-title>
<source><![CDATA[J Am Soc Echocardiogr]]></source>
<year>1996</year>
<numero>9</numero>
<issue>9</issue>
<page-range>599-605</page-range></nlm-citation>
</ref>
<ref id="B25">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Porter]]></surname>
<given-names><![CDATA[TR]]></given-names>
</name>
<name>
<surname><![CDATA[Xie]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Kricsfeld]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Ambrusterbe]]></surname>
<given-names><![CDATA[RW]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Improved myocardial contrast with second harmonic transient response imaging in humans using intravenous perfluorocarbon-exposed sonicated dextrose albumin]]></article-title>
<source><![CDATA[J Am Coll Cardiol]]></source>
<year>1996</year>
<numero>27</numero>
<issue>27</issue>
<page-range>1496-501</page-range></nlm-citation>
</ref>
<ref id="B26">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Crouse]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Kramer]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Stress echocardiography: Technical considerations]]></article-title>
<source><![CDATA[Progress cardiovasc dis]]></source>
<year>2001</year>
<volume>43</volume>
<numero>4</numero>
<issue>4</issue>
<page-range>303-314</page-range></nlm-citation>
</ref>
<ref id="B27">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Moder]]></surname>
<given-names><![CDATA[KG]]></given-names>
</name>
<name>
<surname><![CDATA[Miller]]></surname>
<given-names><![CDATA[TD]]></given-names>
</name>
<name>
<surname><![CDATA[Tazelaar]]></surname>
<given-names><![CDATA[HD]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cardiac involvement in systemic lupus erythematosus]]></article-title>
<source><![CDATA[Mayo Clin Proc]]></source>
<year>1999</year>
<numero>74</numero>
<issue>74</issue>
<page-range>275-284</page-range></nlm-citation>
</ref>
<ref id="B28">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ward]]></surname>
<given-names><![CDATA[MM]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Premature morbidity from cardiovascular and cerebrovascular diseases in women with systemic lupus erythematosus]]></article-title>
<source><![CDATA[Arthritis Rheum]]></source>
<year>1999</year>
<numero>42</numero>
<issue>42</issue>
<page-range>338-346</page-range></nlm-citation>
</ref>
<ref id="B29">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Manzi]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Wasko]]></surname>
<given-names><![CDATA[M-C]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Inflammation-mediated rheumatic diseases and atherosclerosis]]></article-title>
<source><![CDATA[Ann Rheum Dis]]></source>
<year>2000</year>
<numero>59</numero>
<issue>59</issue>
<page-range>321-325</page-range></nlm-citation>
</ref>
<ref id="B30">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cisternas]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Gutierrrez]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
<name>
<surname><![CDATA[Klaassen]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Acosta]]></surname>
<given-names><![CDATA[AM]]></given-names>
</name>
<name>
<surname><![CDATA[acobelli]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cardiovascular risk factors in Chilean patients with rheumatoid arthritis]]></article-title>
<source><![CDATA[J Rheumatol]]></source>
<year>2002</year>
<numero>29</numero>
<issue>29</issue>
<page-range>1619-1622</page-range></nlm-citation>
</ref>
<ref id="B31">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Mutru]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Laakso]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Isomaki]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Koota]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Cardiovascular mortality in patients with rheumatoid arthritis]]></article-title>
<source><![CDATA[Cardiology]]></source>
<year>1989</year>
<numero>76</numero>
<issue>76</issue>
<page-range>71-77</page-range></nlm-citation>
</ref>
<ref id="B32">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Cohn]]></surname>
<given-names><![CDATA[JN]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Arterial compliance to stratify cardiovascular risk more precision in therapeutic decision making]]></article-title>
<source><![CDATA[Am J Hypertens]]></source>
<year>2001</year>
<numero>14</numero>
<issue>14</issue>
<page-range>258S-63S</page-range></nlm-citation>
</ref>
<ref id="B33">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Wong]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Toh]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Wilson]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Roeley]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Karschimkus]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Prior]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Romas]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Clemens]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Dragicevic]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Harianto]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<name>
<surname><![CDATA[Wicks]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[Best]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Jenkins]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Reduced arterial elasticity in rheumatoid arthritis and the relationship to vascular disease risk factors and inflammation]]></article-title>
<source><![CDATA[Arthritis and Rheum]]></source>
<year>2003</year>
<numero>48</numero>
<issue>48</issue>
<page-range>81-89</page-range></nlm-citation>
</ref>
<ref id="B34">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Motoyoshi]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Takaku]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Serum cholesterol-lowering activity of human monocytic colony-stimulating factor]]></article-title>
<source><![CDATA[Lancet]]></source>
<year>1989</year>
<numero>2</numero>
<issue>2</issue>
<page-range>326-327</page-range></nlm-citation>
</ref>
<ref id="B35">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[De Viliers]]></surname>
<given-names><![CDATA[WJ]]></given-names>
</name>
<name>
<surname><![CDATA[Farser]]></surname>
<given-names><![CDATA[IP]]></given-names>
</name>
<name>
<surname><![CDATA[Hughes]]></surname>
<given-names><![CDATA[DA]]></given-names>
</name>
<name>
<surname><![CDATA[Doyle]]></surname>
<given-names><![CDATA[AG]]></given-names>
</name>
<name>
<surname><![CDATA[Gordon]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Macrophage-colony-stimulating factor selectively enhances macrophage scavenger receptor expression and function]]></article-title>
<source><![CDATA[J Exp Med]]></source>
<year>1994</year>
<numero>180</numero>
<issue>180</issue>
<page-range>705-709</page-range></nlm-citation>
</ref>
<ref id="B36">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Horkko]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Miller]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Dudl]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Reaven]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Curtiss]]></surname>
<given-names><![CDATA[LK]]></given-names>
</name>
<name>
<surname><![CDATA[Zvaifler]]></surname>
<given-names><![CDATA[Nj]]></given-names>
</name>
<name>
<surname><![CDATA[Terkeltaub]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Pierangeli]]></surname>
<given-names><![CDATA[SS]]></given-names>
</name>
<name>
<surname><![CDATA[Branch]]></surname>
<given-names><![CDATA[DW]]></given-names>
</name>
<name>
<surname><![CDATA[Palinski]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
<name>
<surname><![CDATA[Witztum]]></surname>
<given-names><![CDATA[JL]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antiphospholipid antibodies are directed against epitopes of oxidized phospholipids: recognition of cardiolipin by monoclonal antibodies to epitopes of oxidized low density lipoprotein]]></article-title>
<source><![CDATA[J Clin Invest]]></source>
<year>1996</year>
<numero>98</numero>
<issue>98</issue>
<page-range>815-825</page-range></nlm-citation>
</ref>
<ref id="B37">
<nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Libby]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The pathogenesis of atherosclerosis]]></article-title>
<person-group person-group-type="editor">
<name>
<surname><![CDATA[Kasper]]></surname>
<given-names><![CDATA[DL]]></given-names>
</name>
</person-group>
<source><![CDATA[Harrison's Principles of Internal Medicine]]></source>
<year>2005</year>
<edition>16</edition>
<page-range>1425-1430</page-range></nlm-citation>
</ref>
<ref id="B38">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Amengual]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Atsumi]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[Khamashta]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
<name>
<surname><![CDATA[Tinahones]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Hughes]]></surname>
<given-names><![CDATA[GRV]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Antibodies against oxidized low-density lipoprotein in antiphospholipid syndrome]]></article-title>
<source><![CDATA[Br J Rheumatol]]></source>
<year>1997</year>
<numero>36</numero>
<issue>36</issue>
<page-range>964-968</page-range></nlm-citation>
</ref>
<ref id="B39">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vaarala]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Alfthan]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Jauhiainen]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Leirsalo-Repo]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Aho]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Palosuo]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Crossreaction between antibodies to oxidized lipoprotein and to cardiolipin in systemic lupus erythematosus]]></article-title>
<source><![CDATA[Lancet]]></source>
<year>1993</year>
<numero>341</numero>
<issue>341</issue>
<page-range>923-925</page-range></nlm-citation>
</ref>
<ref id="B40">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bruce]]></surname>
<given-names><![CDATA[IN]]></given-names>
</name>
<name>
<surname><![CDATA[Gladman]]></surname>
<given-names><![CDATA[DD]]></given-names>
</name>
<name>
<surname><![CDATA[Ibañez]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Urowitz]]></surname>
<given-names><![CDATA[MB]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Single photon emission computed tomography dual isotope myocardial perfusion imaging in women with systemic lupus erythematosus: II. Predictive factors for perfusion abnormalities]]></article-title>
<source><![CDATA[J Rheumatol]]></source>
<year>2003</year>
<numero>30</numero>
<issue>30</issue>
<page-range>288-291</page-range></nlm-citation>
</ref>
<ref id="B41">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Lin]]></surname>
<given-names><![CDATA[JJ]]></given-names>
</name>
<name>
<surname><![CDATA[Hsu]]></surname>
<given-names><![CDATA[HB]]></given-names>
</name>
<name>
<surname><![CDATA[Sun]]></surname>
<given-names><![CDATA[SS]]></given-names>
</name>
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[JJ]]></given-names>
</name>
<name>
<surname><![CDATA[Ho]]></surname>
<given-names><![CDATA[ST]]></given-names>
</name>
<name>
<surname><![CDATA[Kao]]></surname>
<given-names><![CDATA[CH]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Single photon emission computed tomography of technetium-99m tetrofosmin myocardial perfusion imaging in patients with systemic lupus erythematosus: A preliminary report]]></article-title>
<source><![CDATA[Jpn Heart J]]></source>
<year>2003</year>
<numero>44</numero>
<issue>44</issue>
<page-range>83-89</page-range></nlm-citation>
</ref>
<ref id="B42">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Schillaci]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
<name>
<surname><![CDATA[Lagaña]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Danieli]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Gentile]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Tubani]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Baratta]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Scopinaro]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Technetium-99m Sestamibi single-photon emission tomography detects subclinical myocardial perfusion abnormalities in patients with systemic lupus erythematosus]]></article-title>
<source><![CDATA[Eur J Nucl Med]]></source>
<year>1999</year>
<numero>26</numero>
<issue>26</issue>
<page-range>713-717</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
