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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Endogenous testosterone, endothelial dysfunction, and cardiovascular events in men with nondialysis chronic kidney
Mahmut Ilker Yilmaz1, Alper Sonmez, Abdul Rashid Qureshi
1Department Nephrology, School of Medicine, Ankara, Turkey. Juan.jesus.carrero@ki.se
Insights
Low testosterone levels in men with chronic kidney disease (CKD) are linked to poor vascular function and increased cardiovascular risk. Maintaining testosterone may reduce these risks in CKD patients.
Area of Science:
- Endocrinology
- Nephrology
- Cardiology
Background:
- Kidney function decline commonly impairs testosterone production, leading to hypogonadism in men with chronic kidney disease (CKD).
- Testosterone's role in atherosclerosis is suggested in non-renal populations, and low testosterone is linked to mortality in male dialysis patients.
- This study investigates the relationship between testosterone levels, vascular issues, and cardiovascular events in men with non-dialysis CKD.
Purpose of the Study:
- To examine the association between testosterone levels and endothelial dysfunction in men with nondialysis CKD.
- To determine if testosterone levels predict future cardiovascular events in this patient group.
Main Methods:
- A cross-sectional analysis of 239 male CKD patients (stages 1-5) was conducted.
- Flow-mediated dilation (FMD) was assessed, along with routine measurements and serum total and free testosterone.
- Patients were followed for cardiovascular outcomes over a median of 31 months.
Main Results:
- Testosterone levels (total and free) decreased as kidney function worsened.
- Both total and free testosterone independently explained variance in FMD.
- A 22% reduced risk of cardiovascular events was observed for each 1 nmol/L increase in total testosterone, persisting after adjustments.
Conclusions:
- Reduced endogenous testosterone in progressive CKD is associated with endothelial dysfunction.
- Lower testosterone levels exacerbate the risk of future cardiovascular events in men with nondialysis CKD.
Background And Objectives:
Deterioration of kidney function impairs testosterone production, with hypogonadism being common in men with chronic kidney disease (CKD). In nonrenal populations, testosterone is suggested to participate in the atherosclerotic process. In male dialysis patients, we showed that low testosterone increases the risk of mortality. We here studied plausible links among testosterone levels, vascular derangements, and cardiovascular events in nondialysis CKD men.
Design, Setting, Participants, & Methods:
This was a cross-sectional analysis in which flow-mediated dilation (FMD) was assessed in 239 CKD male patients (stages 1 to 5; mean age 52 ± 12 years), together with routine measurements, serum total and free testosterone, and follow-up for cardiovascular outcomes.
Results:
Total and free testosterone levels decreased in parallel with the reduction of kidney function. Multiple regression analyses showed that total and free testosterone significantly and independently contributed to explain the variance of FMD. After a median follow-up of 31 months (range 8 to 35 months), 22 fatal and 50 nonfatal cardiovascular events occurred. In Cox analysis, the risk of cardiovascular events was reduced by 22% for each nanomole-per-liter increment of total testosterone. This reduced risk persisted after adjustment for age, renal function, diabetes mellitus, previous cardiovascular history, C-reactive protein, albumin, and FMD. The same was true for free testosterone concentrations.
Conclusions:
The reduction in endogenous testosterone levels observed with progressive CKD was inversely associated with endothelial dysfunction and exacerbated the risk of future cardiovascular events in nondialysis male CKD patients.
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