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Low circulating androgens and mortality risk in heart failure
  1. G Güder,
  2. S Frantz,
  3. J Bauersachs,
  4. B Allolio,
  5. G Ertl,
  6. C E Angermann,
  7. S Störk
  1. Medizinische Klinik und Poliklinik I, Klinikum der Universität Würzburg, Würzburg, Germany
  1. Correspondence to Dr S Störk, Medizinische Klinik und Poliklinik I – Herz-Kreislaufzentrum, Klinikum der Universität Würzburg, Oberdürrbacher Strasse 6, D – 97080 Würzburg, Germany; stoerk_s{at}klinik.uni-wuerzburg.de

Abstract

Objective Deficiency of anabolic sex steroids is common in heart failure (HF). The pathophysiological implications of this phenomenon, however, have not been fully elucidated. This clinical study investigated the significance of low serum androgen levels in HF.

Design Prospective cohort study.

Patients and Methods In 191 consecutively recruited men with HF (mean age 64 years; New York Heart Association (NYHA) class I–IV 24%/35%/35%/6%) and reduced (ejection fraction (EF) ≤40%, n=96) or preserved (EF >40%, n=95) left ventricular function total and free serum testosterone, dehydroepiandrosterone sulfate (DHEAS) and sex hormone binding globulin (SHBG) were measured. The median observation period was 859 days.

Results During follow-up 53 patients (28%) died. Whereas total serum testosterone was normal in most patients (91%), free testosterone and DHEAS were reduced in 79% and 23%, respectively. DHEAS and free testosterone, but not total testosterone, were inversely associated with NYHA class (both p<0.01). Lower free testosterone and DHEAS and higher SHBG predicted all-cause mortality risk (hazard ratio (HR) 0.89, 95% CI 0.82 to 0.96 per 1 ng/dl free testosterone, p=0.004; HR 0.95, 95% CI 0.89 to 1.00 per 10 μg/dl DHEAS, p=0.058; and HR 1.18, 95% CI 1.05 to 1.33 per 10 nmol/l SHBG, p=0.006, respectively; adjusted for age and NYHA class). However, further adjustment for carefully selected confounding factors abolished these associations.

Conclusion In male HF patients, low serum levels of androgens are associated with adverse prognosis, but this relation is confounded by indicators of a poor health state. The results suggest that low serum androgens develop as a sequel of this progressive multifaceted systemic disorder.

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Footnotes

  • Funding Merck KGaA, Darmstadt, Germany, supported the set-up of the heart failure outpatient clinics. The data analysis was supported by the German Competence Network Heart Failure.

  • Competing interests None.

  • Ethics approval The study was approved by the Ethics Committee of the Medical Faculty of Würzburg University.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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