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Low serum testosterone increases mortality risk among male dialysis patients
Juan Jesús Carrero1, Abdul Rashid Qureshi, Paolo Parini
1Divisions of Renal Medicine and Baxter Novum, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden. juan.jesus.carrero@ki.se
Insights
Low testosterone levels in men undergoing hemodialysis (HD) are linked to higher risks of death and cardiovascular disease (CVD). This suggests hypogonadism may be a treatable factor in chronic kidney disease patients.
Area of Science:
- Nephrology
- Endocrinology
- Cardiovascular Medicine
Background:
- Men on hemodialysis (HD) face poor prognoses and high cardiovascular disease (CVD) risk.
- Low testosterone is a potential cardiovascular risk factor in the general population.
Purpose of the Study:
- To investigate the association between testosterone concentration and mortality in men treated with HD.
- To explore the relationship between testosterone, inflammation, and CVD in this cohort.
Main Methods:
- Prospective observational study of 126 men on HD.
- Measured testosterone levels and followed participants for mortality over 41 months.
- Analyzed associations with inflammatory markers (IL-6, CRP), SHBG, creatinine, and clinical history.
Main Results:
- Testosterone levels inversely correlated with inflammatory markers IL-6 and CRP.
- Men with lower testosterone had significantly higher all-cause and CVD mortality.
- This association persisted after adjusting for multiple clinical factors but not creatinine.
Conclusions:
- Testosterone concentration is inversely associated with mortality and inflammation in men on HD.
- Hypogonadism may represent an additional, treatable risk factor for patients with chronic kidney disease.
Abstract:
Men treated with hemodialysis (HD) have a very poor prognosis and an elevated risk of premature cardiovascular disease (CVD). In the general population, associations between low testosterone concentrations and cardiovascular risk have been suggested. We performed a prospective observational study involving a well characterized cohort of 126 men treated with HD to examine the relationship between testosterone concentration and subsequent mortality during a mean follow-up period of 41 mo. Independent of age, serum creatinine, and sexual hormone binding globulin (SHBG), testosterone levels inversely and strongly associated with the inflammatory markers IL-6 and CRP. Patients with a clinical history of CVD had significantly lower testosterone levels. During follow up, 65 deaths occurred, 58% of which were a result of CVD. Men with testosterone values in the lowest tertile had increased all-cause and CVD mortality (crude hazard ratios [HRs] 2.03 [95% CI 1.24 to 3.31] and 3.19 [1.49 to 6.83], respectively), which persisted after adjustment for age, SHBG, previous CVD, diabetes, ACEi/ARB treatment, albumin, and inflammatory markers, but was lost after adjustment for creatinine. In summary, among men treated with HD, testosterone concentrations inversely correlate with all-cause and CVD-related mortality, as well as with markers of inflammation. Hypogonadism may be an additional treatable risk factor for patients with chronic kidney disease.
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