<?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>0036-3634</journal-id>
<journal-title><![CDATA[Salud Pública de México]]></journal-title>
<abbrev-journal-title><![CDATA[Salud pública Méx]]></abbrev-journal-title>
<issn>0036-3634</issn>
<publisher>
<publisher-name><![CDATA[Instituto Nacional de Salud Pública]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0036-36342009000700017</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[The definition and diagnosis of osteoporosis]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Nordin]]></surname>
<given-names><![CDATA[B. E. C.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Royal Adelaide Hospital  ]]></institution>
<addr-line><![CDATA[Adelaide South Australia 5000]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2009</year>
</pub-date>
<volume>51</volume>
<fpage>s132</fpage>
<lpage>s133</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0036-36342009000700017&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0036-36342009000700017&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0036-36342009000700017&amp;lng=en&amp;nrm=iso"></self-uri></article-meta>
</front><body><![CDATA[ <p align="right"><font size="2" face="Verdana"><b>CL&Aacute;SICO</b></font></p>     <p>&nbsp;</p>     <p><font size="4" face="verdana"><b>The definition and diagnosis of osteoporosis</b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana"><b>B. E. C. Nordin</b></font></p>     <p><font size="2" face="Verdana">Royal Adelaide Hospital, Adelaide, South Australia    5000</font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font size="2" face="Verdana">Although    we are inclined to think of osteoporosis as a modern disease, particularly in    view of its apparently greater prevalence in the more prosperous societies of    the world, the contribution of bone fragility to fractures in the elderly has    been known for at least 200 years. It is difficult to say when the term "osteoporosis"    was first used in the modern sense, but it was certainly employed by pathologists    in the mid&#45;nineteenth century and was clearly distinguished from osteomalacia    by Pommer almost exactly 100 years ago.</font></p>     ]]></body>
<body><![CDATA[<p><font size="2" face="Verdana"> At the clinical level the crush fracture syndrome    was still being confused with osteomalacia in the 1930's, but by the end of    that decade Albright had definitively identified it with osteoporosis, which    he defined as "too little calcified bone," and his teaching has been    amply confirmed. We now recognize that osteoporosis is not only the principal    cause of spontaneous vertebral compression but is also a major contributor to    most fractures in the elderly. It is also common ground that osteoporosis represents    a reduction in the volume of bony tissue relative to whole bone volume. Histomorphometry    has established this concept beyond all reasonable doubt by showing that crush    fractures in the spine are generally associated with trabecular bone volumes    in the iliac crest below about 15% compared with volumes in normal young adults    of about 20 to 30%. From this, it has become common practice to equate vertebral    compression with osteoporosis and to use it in the selection of patients for    clinical trials. It has proved a useful approach which was justified in the    1970's when bone densitometry was in its infancy but has been extrapolated to    the point where a fracture (any fracture) is considered essential to the diagnosis    of osteoporosis &#150;or even diagnostic of it.</font></p>     <p><font size="2" face="Verdana"> This practice is not only undesirable but positively    misleading. While it is true that spontaneous vertebral compression, <I>because    </I>it is spontaneous, generally denotes the presence of severe osteoporosis,    this is not true of other fractures, which nearly always involve an element    of trauma. Whether a bone breaks or not depends on the relation between the    severity of the trauma and the strength of the bone, the main determinant of    which is its "density," i.e., its relative content of bony tissue.    What osteoporosis does is to increase the fracture risk, not cause the fracture.    It is a simple matter to show, by comparing fracture and nonfracture cases,    that fracture risk is a continuous variable which rises as bone density falls,    though not, of course, in a simple linear manner. As indicated above, the invoking    of a fracture to justify a diagnosis of osteoporosis dates from the days before    high precision densitometry; it should no longer be the practice of specialists    with access to the new technology. There was a time when hyponatremia was recognized    from the state of the tongue, diabetes from the taste of the urine, and anemia    from the color of the skin. These signs, though still of clinical interest,    do not form the basis of contemporary definition and diagnosis in these fields.    Nor should analogous thinking form the basis of definition and diagnosis in    the bone field.</font></p>     <p><font size="2" face="Verdana"> Few workers would dispute Albright's definition    of osteoporosis as "too little calcified bone." Yet, many are reluctant    to follow it through to its logical conclusion. We can now easily measure the    amount of calcified bone, or at least the amount of mineral in a bone, which    is generally the same thing. If it is reduced, osteoporosis must be present    (discounting the rare case of osteomalacia), and the main problem is to define    the standard against which this reduction should be measured. For this there    are ample precedents in other fields of clinical physiology where the normal    range is usually derived from young healthy adults. The same standard should    be applied to bone. In any given laboratory, using any given technique in any    given part of the skeleton, I submit that osteoporosis is present when the concentration    of bone (mineral) lies more than two standard deviations below the mean of young    adults of the same sex. If forearm measurements are used, this implies, of course,    that some 50% of women have osteoporosis by age 65 and nearly 100% by age 80.    These figures will be rather different if vertebral densitometry, or some other    technique or site, is used. But the principle remains the same. Only whole body    measurements can overcome the problem of regional differences in the skeleton,    but they are subject to more error than regional measurements and are less generally    available.</font></p>     <p><font size="2" face="Verdana"> The concept that all women and most men become    osteoporotic, if they live long enough, is distasteful to some. Yet, the fact    that blood pressure rises with age, and that hypertension of some degree affects    virtually everyone sooner or later, has not prevented physicians from defining    normal blood pressure in terms of the young adult range. In assessing its significance    in an individual, however, age must be taken into account, and the same is true    of bone. In absolute terms, a bone density measurement below the young normal    range denotes osteoporosis and increased fracture risk &#150;at least in that bone,    if not elsewhere&#150; but the clinical significance of the measurement is also a    function of the age of the subject; a value which, though osteoporotic, lies    within the normal range for the age of the subject means something different    from a value which is low for age. By loose analogy with hypertension, the latter    may be termed, "accelerated osteoporosis," the former, "simple    osteoporosis"; bearing in mind that the measurement is only <I>strictly    </I>applicable to the measured bone. In patients with two or more crush fractures,    trabecular bone density is generally so low that it represents "accelerated    osteoporosis" at any age &#150;which is why these cases differ in so many respects    from subjects of the same age without crush fractures. But even here it is likely    that classification by fracture will yield to classification by densitometry    because of the inherently greater precision of the latter.</font></p>     <p><font size="2" face="Verdana"> It is surprising that osteoporosis research    has made the progress it has when the central object of the work lacks a common    definition. Such a definition is clearly overdue. Perhaps this Guest Editorial    will help to fill the gap.</font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <!-- ref --><p><font size="2" face="Verdana">From: Nordin BEC. The definition and diagnosis    of osteoporosis. Calcified Tissue Int 1987;40:57&#45;58.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=9284068&pid=S0036-3634200900070001700001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --> Reprinted with kind permission    of Springer Science and Business Media.</font></p>      ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Nordin]]></surname>
<given-names><![CDATA[BEC]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[The definition and diagnosis of osteoporosis]]></article-title>
<source><![CDATA[Calcified Tissue Int]]></source>
<year>1987</year>
<volume>40</volume>
<page-range>57-58</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
