In older men an optimal plasma testosterone is associated with reduced all-cause mortality and higher dihydrotestosterone with reduced ischemic heart disease mortality, while estradiol levels do not predict mortality

Bu B. Yeap, Helman Alfonso, Paul Chubb, David J. Handelsman, Graeme J. Hankey, Osvaldo P. Almeida, Jonathan Golledge, Paul E. Norman, Leon Flicker

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Context: Testosterone (T) levels decline with age and lower T has been associated with increased mortality in aging men. However, the associations of its metabolites, dihydrotestosterone (DHT) and estradiol (E-2), with mortality are poorly defined.

Objective: We assessed associations of T, DHT, andE(2) with all-cause and ischemic heart disease (IHD) mortality in older men.

Participants: Participants were commun(i)ty-dwelling men aged 70 to 89 years who were residing in Perth, Western Australia.

Main Outcome Measures: Plasma total T, DHT, and E-2 were assayed using liquid chromatography-tandem mass spectrometry in early morning samples collected in 2001 to 2004 from 3690 men. Deaths to December 2010 were ascertained by data linkage.

Results: There were 974 deaths (26.4%), including 325 of IHD. Men who died had lower baseline T (12.8 +/- 5.1 vs 13.2 +/- 4.8 nmol/L [mean +/- SD], P = .013), DHT (1.4 +/- 0.7 vs 1.5 +/- 0.7 nmol/L, P = .002), and E-2 (71.6 +/- 29.3 vs 74.0 +/- 29.0 pmol/L, P = .022). After allowance for other risk factors, T and DHT were associated with all-cause mortality (T: quartile [Q] Q2:Q1, adjusted hazard ratio [HR] = 0.82, P = .033; Q3: Q1, HR = 0.78, P = .010; Q4:Q1, HR = 0.86, P = .05; DHT: Q3:Q1, HR = 0.76, P = .003; Q4:Q1, HR = 0.84, P > .05). Higher DHT was associated with lower IHD mortality (Q3:Q1, HR = 0.58, P = .002; Q4:Q1, HR = 0.69, P = .026). E-2 was not associated with either all-cause or IHD mortality.

Conclusions: Optimal androgen levels are a biomarker for survival because older men with midrange levels of T and DHT had the lowest death rates from any cause, whereas those with higher DHT had lower IHD mortality. Further investigations of the biological basis for these associations including randomized trials of T supplementation are needed.

Original languageEnglish
Pages (from-to)E9-E18
Number of pages10
JournalJournal of Clinical Endocrinology & Metabolism
Issue number1
Early online date20 Nov 2013
Publication statusPublished - Jan 2014

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