Low serum testosterone, arterial stiffness and mortality in male haemodialysis patients

John Kyriazis1, Ioannis Tzanakis, Kostas Stylianou

  • 1Department of Nephrology, General Hospital of Chios, Chios, Greece. jks@otenet.gr

Insights

Low testosterone levels in male hemodialysis patients are linked to higher risks of cardiovascular disease (CVD) and death. Increased arterial stiffness may explain this association, highlighting a potential mechanism for mortality in this population.

Area of Science:

  • Nephrology
  • Endocrinology
  • Cardiovascular Medicine

Background:

  • Low testosterone levels are associated with increased all-cause and cardiovascular disease (CVD) mortality in the general population.
  • Accelerated arterial stiffness is a recognized cardiovascular risk factor.
  • Male hemodialysis (HD) patients exhibit generalized arterial stiffening, necessitating investigation into testosterone's role in their mortality risk.

Purpose of the Study:

  • To explore the association between testosterone levels and the risk of death in male HD patients.
  • To investigate the potential role of arterial stiffness as a mediator in this association.

Main Methods:

  • A three-center prospective observational study involving 111 male HD patients.
  • Baseline assessment included measurement of male sex hormones and pulse wave velocity (PWV).
  • Patients were followed up for CVD and all-cause mortality.

Main Results:

  • Testosterone deficiency (levels <8 nmol/L) was identified in 54 patients.
  • During a median follow-up of 37 months, 49 deaths occurred (28 due to CVD).
  • Testosterone deficiency was associated with increased CVD and all-cause mortality, even after adjustments for confounders. This association with CVD mortality was attenuated after adjusting for PWV, which was inversely related to testosterone levels.

Conclusions:

  • Testosterone deficiency in male HD patients is significantly associated with increased CVD and all-cause mortality.
  • Increased arterial stiffness is identified as a potential mechanism linking testosterone deficiency to higher mortality in this cohort.
Abstract

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