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Revista mexicana de urología

versión On-line ISSN 2007-4085versión impresa ISSN 0185-4542

Rev. mex. urol. vol.82 no.1 Ciudad de México ene./feb. 2022  Epub 20-Jun-2022

https://doi.org/10.48193/revistamexicanadeurologa.v82i1.741 

Original articles

Abdominal aorta calcifications in patients with kidney stones, is there a link?

Calcificaciones de la aorta abdominal en pacientes con litiasis renal, ¿existe un vínculo?

Mario Basulto-Martínez1  * 
http://orcid.org/0000-0001-7589-8909

Guillermo José Cueto Vega1 
http://orcid.org/0000-0001-6385-2380

Amanda Elisa Arenas-Aquino1 
http://orcid.org/0000-0001-6914-7834

José Enrique Espinosa Aznar1 
http://orcid.org/0000-0001-8465-288X

Dalia Montserrat Meza-Bosquez2 
http://orcid.org/0000-0002-0174-4234

Rodrigo Ortegón-Gallareta2 
http://orcid.org/0000-0003-3348-1827

Antonio Esqueda-Mendoza1 
http://orcid.org/0000-0001-8525-9166

Juan Pablo Flores Tapia1 
http://orcid.org/0000-0002-5203-1410

1Secretaría de Salud, Hospital Regional de Alta Especialidad de la Península de Yucatán, Yucatán, México.

2Escuela de Medicina, Universidad Anáhuac Mayab, Yucatán, México.


Abstract

Objective:

To investigate the correlations between abdominal aortic calcifications (AAC) and the underlying urinary metabolic abnormalities in stone-formers (SF).

Methods:

Patients with a 24 h urinary panel and computed tomography scan were included. The Kauppila Score (KS) was used to quantitatively assess AAC; clinical data and stone information were also recorded. The Spearman correlation was utilized.

Results:

A total of 54 patients were included, the mean age was 46.4±11.2, 75.9% were female, and 59.3% had AAC. Hypertension and AAC were associated (p=0.026), and the KS was higher in patients with hypertension. Hypocitraturia (98.1%) and hypercalciuria (16.7%) were the most frequent urinary abnormalities, but they were unrelated to AAC (p>0.05). The 24 urinary panel, blood biochemistry, stone burden and hardness, and body mass index were not correlated to the KS (p>0.05).

Limitations:

This work had the following limitations: its retrospective nature, a relatively small sample, and the lack of an automated informatics-based assessment of AAC.

Conclusion:

The link between cardiovascular diseases and kidney stones is still to be elucidated. Our finding differs from the other few studies reported on the literature, as no correlation was found between AAC and the urinary metabolic abnormalities in SF.

Keywords: Kidney stones; urolithiasis; kidney calculi; hypertension; hypocitraturia

Resumen

Objetivo:

Investigar la correlación entre la calcificación aórtica abdominal (AAC) y las alteraciones urinarias metabólicas subyacentes en formadores de litiasis (SF).

Métodos:

Pacientes con perfil metabólico urinario de 24 hrs y tomografía computarizada fueron incluidos. Se utilizó el índice de Kauppila (KS) para el análisis cuantitativo de las AAC; y se recabaron datos clínicos y características del lito. Se empleó la prueba de correlación de Spearman.

Resultados:

Se incluyeron 54 pacientes, con media de edad de 46.4±11.2, 75.9% fueron mujeres y el 59.3% tuvo AAC. La hipertensión y las AAC estuvieron asociadas (p=0.026), y el KS fue mayor en pacientes hipertensos. La hipocitraturia (98.1%) e hipercalciuria (16.7%) fueron las alteraciones urinarias más frecuentes, pero no se relacionaron con las AAC (p>0.05). El perfil metabólico urinario, pruebas bioquímicas, dureza y carga litiásica y el índice de masa corporal no presentaron correlación con el KS (p>0.05).

Limitaciones del estudio:

El trabajo cursa con limitaciones tal como la naturaleza retrospectiva, una muestra pequeña y la falta evaluación automatizada de las calcificaciones en la aorta abdominal.

Conclusión:

El vínculo entre las enfermedades cardiovasculares y la litiasis renal necesita ser aclarado. Nuestros resultados contrastan con los poco reportados en la literatura, ya que no encontramos correlación entre las AAC y las alteraciones metabólicas urinarias SF.

Palabras clave: Litiasis renal; urolitiasis; cálculos renales; hipertensión; hipocitraturia

Introduction

The prevalence of kidney stones has been steadily increasing worldwide and this increase has been more pronounced in undeveloped countries.1,2 This recurrent disease has a negative impact on patients’ quality of life, and can progress to kidney function impairment. The environmental and lifestyle risk factors for the development of kidney stones have been highlighted extensively. Furthermore, genetic alterations associated with the underlying urinary metabolic abnormalities that lead to kidney stones, have also been described in recent years.3-5

Assessing the stone-formers (SF) urinary metabolism is paramount, as it reflects, to an extent, dietary habits which provide information on hydration and acid-base status. Certain substances in urine work, whether as inhibitors or facilitators of stone aggregation and nucleation, the first steps of lithogenesis. In average subjects, urine is virtually always metastable to calcium oxalate and other substances.6 Keeping those substances balanced is among the most important recurrence-prevention strategies, and these alterations can be detected trough a 24 h urinary panel (24UP), giving place to tailored managements to restore such balance based on diet, supplements and/or drugs.

On the other hand, a link between metabolic diseases and kidney stones has been suggested. Recently, the pathophysiological pathways through which type 2 diabetes and insulin resistance turn out in more acidic urine have been outlined, resulting in a higher risk for kidney stones.7,8 Mexico is considered as the country with the highest prevalence of obesity; in Southeast Mexico, the prevalence of overweight/obesity is 72.5%.9 Likewise, a high prevalence of type 2 diabetes (9.2%) and hypertension (25.5%) was reported locally in the most recent National Health and Nutrition Survey.10,11 Moreover, hypertension and coronary artery disease, which have a risk relation with obesity and type 2 diabetes, have also been related to kidney stones.8 Although the link remains unclear, hypertension is more prevalent in SF than in subjects without kidney stones.12,13

Endothelial dysfunction and atherosclerosis are associated to oxidative stress, which is a common pathway for kidney stones development.14 Furthermore, vascular calcifications, especially abdominal aortic calcifications (AAC), serves as an indicator of vascular damage and mortality.15 Recently, Patel et al. reported that SF with AAC had lower urinary citrate and pH.16 In this work we aimed to assess the relation of AAC and the 24UP in SF.

Material and methods

This study was approved by the Ethics and Research Committees from the Hospital Regional de Alta Especialidad de la Península de Yucatán. The prospectively collected database, comprising data of SF treated at the Hospital Stone Clinic was retrospectively reviewed. Patients who met the following criteria were included: (i), 18 years or older; (ii), complete medical record; (iii), digital images from a non-contrast computed tomography (NCCT) scan; (iv), a 24UP including urinary calcium, citrate and pH, and blood tests including glucose, creatinine, calcium, vitamin D and PTH.

NCCT assessment

Every NCCT scan was independently assessed by two urologists (MBM, AEAA), from which the following data was retrieved: stone burden, Hounsfield Units (HU) and whether any AAC was present. For AAC quantitative assessment, the Kauppila Score (KS) was utilized, in which the abdominal aorta is axially split into four, matching the vertebral L1-L4 levels, and then coronally into anterior and posterior, resulting in 8 sections. Each section is assesed for AAC and graded according to the calcifications observed as follows: 0, no calcifications; 1, up to 1/3 of the section; 2, beyond 1/3 of the section; 3, beyond 2/3 of the section. Finally, all of the sections’ values are added to obtain the KS, which ranges between 0-24 (figure 1).17

Eight sections are obtained by splitting the abdominal aorta axially in the L1-L4 vertebral levels,4 which are then again divided into anterior and posterior sections.8 Each of the 8 sections is assessed for calcifications, and a 0-3 score is given as follows: 0, no calcifications; 1, up to 1/3; 2, more than 1/3; 3, more than 2/3. Then, all the sections values are added to get a final score between 0 and 24. The image provides an example of a score of 1 (L2 anterior), plus 2 (L1 posterior), and 3 (L3 anterior), thus a total Kauppila Score of 6.

Figure 1 Kauppila Score for quantitative assessment of the abdominal aortic calcifications 

Biochemical analysis

Urine and blood samples from all patients were processed at the hospital clinical laboratory and the following methods were used: calcium, ionic method; pH, potentiometry; citrate and glucose, enzymatic standardized methods; vitamin D and PTH, chemiluminescent method.

Statistical analysis

All analyses were conducted through the Statistical Package for the Social Sciences (SPSS Inc., V. 21, Chicago, IL). The categorical data was presented as frequencies, whereas quantitative data was presented as mean ± standard deviation or median (percentiles 25th - 75th) according to its distribution, tested by the Kolmogorov-Smirnov method. Calcium/creatinuria and citrate/creatinuria urinary ratios were calculated to avoid the kidney function’s effect. The categorical data was compared through X2 test and the quantitative data by a T-test or U-Mann-Whitney test, as appropriate. The Spearman test was used for correlations. P values of <0.05 were considered significant.

Results

A total of 54 patients met the criteria and were included in the study. The mean age was 46.4±11.2, AAC were observed in 59.3%, and 75.9% of the patients were female. Patients’ characteristics and demographics are presented in Table 1. The KS was 3 (2-5.7) and it was moderately correlated with age (p<0.001, r=0.48). Moreover, hypertension and AAC were associated (p=0.026), as 76.5% of hypertense patients had AAC; and the KS was higher in patients with hypertension [4 (2-8) vs 2 (2-4), p=0.026].

Table 1 Initial characteristics and demographics of stone-formers 

Gender (%)
Male 24.1
Female 75.9
Age 46.4 ± 11.2
BMI (kg/m2) 31.4±5.2
Hypertension (%) 31.5
Type 2 diabetes (%) 20.4
AAC (%) 59.3
Kauppila Score 3 (2 - 5.7)
Stone burden (cm3) 8.5 (4 - 14.2)
HU 1002 (631.7 - 1279.6)
Glycemia (mg/dL) 95.9 (89.4 - 106.5)
Urea, serum (mg/dL) 38.2 (22.7 - 57.6)
Creatinine, serum (mg/dL) 1.09 (0.80 - 1.82)
Calcium, serum (mg(dL) 8.9 (8.3 - 9.4)
Urinary calcium (mg/24h) 115.4 (53.8 - 168.2)
Creatinuria (mg/24h) 65 (39.5 - 142.2)
Urinary volume (ml/24 h) 2147.5 (1697.5 - 2797.5)
PTH (pg/mL) 46.4 (25.1 - 74.9)
Vitamin D (pg/mL) 22.7 (17.4 - 31)
Urinary pH 6 (5 - 7)

AAC, Abdominal aortic calcifications; BMI, body mass index; HU, Hounsfield Units.

Hypocitraturia (<320 mg/24h) and hypercalciuria (>200 mg/24h) were observed in 98.1% and 16.7% of the patients, respectively, and no association with AAC was found (p=0.403 y p=0.620, respectively). Table 2 shows a comparison between SF with, and without AAC. No correlations between the KS and 24UP, blood analytes, stone burden, HU and body mass index (BMI) were found (all p>0.05).

Table 2 Differences between stone-formers with and without abdominal aortic calcifications 

AAC No AAC P
Age 50.5 (43.2 -57.7) 41.5 (34.7-49.2) 0.004*
Gender (%) 0.033*
- Male 34.4 9.1
- Female 65.6 90.9
BMI (Kg/m2) 31.1 (28.6-35.4) 31.6 (26.6-35.7) 0.867
Hypertension (%) 40.6 18.2 0.026*
Type 2 diabetes (%) 25 13.6 0.308
Hypocitraturia (%) 96.9 100 0.403
Hypercalciuria (%) 18.8 13.6 0.620
Stone burden (cm3) 8.6 (4.8-14.7) 8.3 (3.1-14.1) 0.712
HU 1037.5 (654.7-1315.1) 984 (626.2-1246.4) 0.460
Glycemia (mg/dL) 97.6 (91.5-107.7) 94.7 (86.3-104.6) 0.439
Urea, serum (mg/dL) 38.2 (28.3-56.6) 35.2 (20.7-69.1) 0.509
Creatinine, serum (mg/dL) 1.09 (0.82-1.69) 1.07 (0.75-2.80) 0.874
Calcium, serum(mg/dL) 8.95 (8.40-9.50) 8.65 (8.17-9.32) 0.481
Vitamin D (pg/mL) 22.7 (19-32) 22.4 (15.3-30.6) 0.470
PTH (pg/mL) 43.7 (25-80.9) 51.7 (26-69) 0.826
Urinary volume (ml/24h) 2228.5 (1900.5-2886) 2020 (1182.5-2720) 0.117
Creatinuria (mg/24h) 1.17 (0.87-1.40) 1.06 (0.85-1.18) 0.315
Urinary pH 6 (5-6.9) 6 (5-7) 0.870
Urinary citrate (mg/24h) 70 (36.5-140) 59 (40.8-165.8) 0.895
Urinary calcium (mg/24h) 123.6 (61-177.3) 95.2 (50.15- 168.2) 0.374
calcium/creatinuria ratio 0.14 (0.07-0.18) 0.10 (0.04-0.18) 0.549
citrate/creatinuria ratio 59.4 (31-119.7) 65.5 (35.7-197.1) 0.476

AAC, Abdominal aortic calcifications; BMI, body mass index; HU, Hounsfield Units.*Statistically significant

Discussion

Nephrolithiasis is a public health challenge, as it overburdens health care services due to its recurrent nature and spreading generic preventive recommendations which suit all types of stones is not always feasible, because of the phenotype complexity. Therefore, the generation of information regarding the pathophysiological pathways implied is highly appreciated, as it can serve as a beacon for guiding further research, and strategies which provide foundations for more robust and personalized recommendations. In recent years, the prevalence of kidney stones has been increasing, and it has been suggested as a result of the parallel prevalence increase of metabolic diseases, such as obesity, diabetes and hypertension.

Other studies have associated hypertension and kidney stones; a link that was first described by Tibblin in the 1960’s.18 Similarly, Borghi et al., found that patients with hypertension had higher incidence of stone episodes when compared with subjects without hypertension (14 vs 3%).19 Despite the causal relationship being unclear, shared factors between urolithiasis and hypertension have been described. Shang et al., suggested that calcium metabolism might play a role in the pathogenesis of both diseases; then, they suggested that the components of the metabolic syndrome, which are also highly prevalent in patients with urolithiasis and/or hypertension, might signal to insulin resistance as a common pathophysiological pathway. Hence, patients with urolithiasis and/or hypertension are more likely to develop chronic kidney disease. Finally, inflammation and oxidative stress have also been recently suggested as possible link.13 Inflammation can cause renal vasoconstriction, ischemia, and injury, rising blood pressure. Likewise, inflammation and oxidative stress can damage epithelial renal cells, becoming exposed to crystallization in the collecting ducts. Thus, observational studies have shown hypertension as a predictive factor for the recurrence of kidney stones.20-22

AAC are observed in over 80% of patients >65 years-old, and this condition has been proposed as a predictor for cardiovascular events and mortality, and quantitative scores have been reported. Kauppila et al., retrieved data from the Framingham cohort and developed a score based on calcification severity assessed by its extension. As this score was first reported on x-ray, no information on attenuation is considered.17

Our study showed that hypertension has a role in the risk of kidney stones development, but the causality link is yet to be elucidated. However, in SF, the prevalence of hypertension (31.5%) and type 2 diabetes (20.4%), exceeds the one reported in Mexico’s Southeast overall population (13.6% and 9.2%, respectively; both p<0.05). Moreover, the prevalence of hypertension was higher in SF with AAC (Table 2) and the KS was higher in SF with hypertension (p=0.026).

Other studies have addressed these aspects and are enlisted in table 3. A high prevalence of hypertension in SF in Ohio (67%) was reported by Patel et al., and it was also significantly higher in SF with AAC (85.5%).16 Likewise, a higher prevalence of type 2 diabetes was reported in SF with AAC, which was not observed in our study. Similarly, Shavit et al. conducted a retrospective case-control study and found that hypertension was more prevalent in SF than in non-stone-former controls (10% vs 2%, p=0.002), but the frequency of type 2 diabetes was comparable (35% vs 9%, p=0,07). Even though no sub-analysis was conducted between patients with AAC, a comparable rate was reported between SF (38%) and control subjects (35%). These outcomes showed that older age and male sex were associated with ACC. According to that, at least up to one third of SF has a previous history of hypertension, and this holds a relation with AAC, which are observed in 38-64%.23

Table 3 Findings of recent studies of abdominal aortic calcifications in stone-formers 

Population Age BMI (Kg/m2) Stone burden (mm3) HTN (%) T2D (%) Hypercalciuria (%) Hypocitraturia (%) Outcomes
Shavit et al. 2015.16 N=111 NA NA AAC severity was associated with kidney stones after sex, age, HTM, T2D, smoking and renal function adjustment.
-57 SF (38% AAC) 47±14 35 10 56 10.5
-54 Non-SF (35% AAC) 47±13 9 2 -- --
Patel et al. 2017.23 N=97 SF 59±17 31.2±8.3 179±0357 67 23.7 NA NA Older age, lower citrate and pH, higher stone burden, higher frequency of HTN and T2D in SF with AAC. 80% of uric acid SF had AAC
-64 with AAC (64%) 68.6±11.2 31.3±7.9 66±171 85.5 33.9
-33 no AAC 43.6±12.3 31.3±9.1 247±420 34.3 5.7
This work N=54 SF 46.4±11.2 31.4±5.2 850 (400-142) 31.5 20.4 16.7 98.1 HTN prevalence was higher in SF with AAC, but no correlation between urinary pH, citrate, and calcium, and AAC severity was observed.
-32 with AAC (59.3%) 50.5 (43.2-57.7) 31.1 (28.6-35.4) 860 (480-147) 40.6 25 18.8 96.9
-22 no AAC 41.5 (34.7-49.2) 31.6 (26.6-35.7) 830 (310-141) 18.2 13.6 13.6 100

AAC, abdominal aortic calcifications; BMI, body mass index; HTN, hypertension; SF, stone-formers; T2D, type 2 diabetes.

The similarities between our outcomes and those reported by Patel et al., might respond in part to the high BMI found in both populations. However, the overall lower hypertension rate might be explained by the younger population reported here (Table 3). Interestingly, our cohort had larger stone-burden, but the meaning of this finding is yet to be explored. Furthermore, we did not find any correlation between urinary metabolism and AAC. The work by Patel et al., reports that urinary pH and citrate were lower, and stone burden was higher in SF with AAC. Moreover, 80% of uric acid SF had AAC. This finding is consistent with the pathophysiological pathway of impaired ammonia excretion due to insulin resistance in obesity, which turns out in more acidic urine (low pH, low citrate), facilitating the aggregation of uric acid stones, but also calcium-containing stones. Interestingly, the higher proportion of AAC was observed among uric acid SF, suggesting a common link between vascular calcifications, hypertension and kidney stones.16

We did not find any correlation between 24UP and AAC, contrasting with the results of Patel et al., who reported a correlation with urinary citrate and pH and AAC. Regarding citrate, an explanation is the high prevalence and severity of hypocitraturia reported in Southeast Mexico. Hence, this work has a low proportion of SF without hypocitraturia (<2%), which hinders comparisons, as we mostly faced a hypocitraturic SF cohort.

A possible role of vascular diseases in kidney stones is undeniable, as cumulative evidence points toward this direction. Nevertheless, the link still needs to be explored. Obesity and vascular diseases have common backgrounds which might be evident as AAC, and somehow serve as an indicator for the urinary metabolism of SF. However, this study did not find any correlation between AAC and urinary calcium, citrate and pH, but further prospective case-control studies are warranted.

This work has the following limitations: (i), its retrospective nature; (ii), a relatively small sample; (iii), the lack of an automated informatics-based assessment of AAC.

Conclusions

The search for a pathophysiological link between obesity, cardiovascular diseases and kidney stones is sure to bring clinically impactful outcomes. As the association of these diseases increases, the causality is still to be determined. However, even if AAC, which indicate vascular disease, somehow reveal SF’s urinary metabolisms, it remains controversial and further endeavors are needed.

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Received: December 28, 2020; Accepted: January 14, 2022

*Corresponding author: Mario Basulto-Martínez. Calle 7 por 20 y 22 Núm. 433, Fraccionamiento Altabrisa, Mérida, Yucatán. C.P. 97130. Correo electrónico: basultourologia@gmail.com

Citation: Basulto-Martínez M., Cueto-Vega G. J., Arenas-Aquino A. E., Espinosa-Aznar J. E., Meza-Bosquez D. M., Ortegón-Gallareta R,, et al. Abdominal aorta calcifications in patients with kidney stones, is there a link? Rev Mex Urol. 2022;82(1):pp: 1-11.

Financing: No sponsorship was received to write this article.

Conflict of interest: The authors declare no conflicts of interest.

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License