Circulating Androgen Concentrations and Risk of Incident Heart Failure in Older Men: The Cardiovascular Health Study

Author:

Njoroge Joyce N.1ORCID,Tressel William2ORCID,Biggs Mary L.2ORCID,Matsumoto Alvin M.23ORCID,Smith Nicholas L.2ORCID,Rosenberg Emily45ORCID,Hirsch Calvin H.6ORCID,Gottdiener John S.7ORCID,Mukamal Kenneth J.58ORCID,Kizer Jorge R.19ORCID

Affiliation:

1. University of California San Francisco San Francisco CA

2. University of Washington Seattle WA

3. Veterans Affairs Puget Sound Health Care System Seattle WA

4. Brigham and Women’s Hospital Boston MA

5. Harvard Medical School Boston MA

6. University of California Davis Davis CA

7. University of Maryland Baltimore MA

8. Beth Israel Deaconess Medical Center Boston MA

9. San Francisco Veterans Affairs Health Care System San Francisco CA

Abstract

Background Circulating androgen concentrations in men decline with age and have been linked to diabetes and atherosclerotic cardiovascular disease (ASCVD). A similar relationship has been reported for low total testosterone and incident heart failure (HF) but remains unstudied for free testosterone or the more potent androgen dihydrotestosterone (DHT). We hypothesized that total/free testosterone are inversely related, sex hormone–binding globulin is positively related, and total/free DHT bear a U‐shaped relationship with incident HF. Methods and Results In a sample of men from the CHS (Cardiovascular Health Study) without atherosclerotic cardiovascular disease or HF, serum testosterone and DHT concentrations were measured by liquid chromatography–tandem mass spectrometry, and sex hormone–binding globulin by immunoassay. Free testosterone or DHT was calculated from total testosterone or total DHT, sex hormone–binding globulin, and albumin. We used Cox regression to estimate relative risks of HF after adjustment for potential confounders. In 1061 men (aged 76±5 years) followed for a median of 9.6 years, there were 368 HF events. After adjustment, lower calculated free testosterone was significantly associated with higher risk of HF (hazard ratio [HR], 1.14 [95% CI, 1.01–1.28]). Risk estimates for total testosterone (HR, 1.12 [95% CI, 0.99–1.26]), total DHT (HR, 1.10 [95% CI, 0.97–1.24]), calculated free dihydrotestosterone (HR, 1.09 [95% CI, 0.97–1.23]), and sex hormone–binding globulin (HR, 1.07 [95% CI, 0.95–1.21]) were directionally similar but not statistically significant. Conclusions Calculated free testosterone was inversely associated with incident HF, suggesting a contribution of testosterone deficiency to HF incidence among older men. Additional research is necessary to determine whether testosterone replacement therapy might be an effective strategy to lower HF risk in older men.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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