Modest opposite associations of endogenous testosterone and oestradiol with left ventricular remodelling and function

J B Ruige1, E R Rietzschel, M L De Buyzere

  • 1Department of Endocrinology, Ghent University Hospital, Ghent University, Ghent, Belgium. johannes.ruige@ugent.be

Insights

In healthy men, testosterone and estradiol show opposite links to left ventricle systolic function. This may explain why testosterone doesn't increase cardiovascular disease risk in this group.

Area of Science:

  • Cardiovascular Endocrinology
  • Reproductive Endocrinology
  • Clinical Cardiology

Background:

  • Endogenous testosterone generally does not elevate cardiovascular disease (CVD) risk in healthy middle-aged men.
  • Potential explanations include differential testosterone effects or interference with estradiol's cardiovascular functions.
  • Understanding these hormonal influences on cardiac function is crucial for CVD risk assessment.

Purpose of the Study:

  • To investigate the associations between endogenous testosterone, estradiol, and left ventricular structure and function.
  • To explore the potential mechanisms behind the neutral effect of testosterone on CVD risk in healthy men.
  • To elucidate the distinct roles of testosterone and estradiol in cardiac performance.

Main Methods:

  • Cross-sectional population study of 1223 healthy men, aged 46 (6) years.
  • Echocardiography was used to assess left ventricular structure and function.
  • Linear regression analyses examined associations between sex steroid concentrations and cardiac parameters, adjusting for multiple covariates.

Main Results:

  • Testosterone was inversely associated with ejection fraction (EF) and systolic tissue Doppler imaging indices.
  • Estradiol showed a positive association with EF.
  • These associations were statistically significant and consistent for both free and total sex steroid concentrations.

Conclusions:

  • Testosterone and estradiol exhibit opposing associations with left ventricle systolic function in healthy middle-aged men.
  • These findings offer a partial explanation for the overall neutral impact of testosterone on CVD risk in this demographic.
  • Further research is warranted to fully elucidate the complex interplay of sex hormones in cardiovascular health.

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