Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study. Issue 4 (April 2020)

• Record Type: Journal Article
• Authors: Schederecker, Florian; Cecil, Alexander; Prehn, Cornelia; Nano, Jana; Koenig, Wolfgang; Adamski, Jerzy; Zeller, Tanja; Peters, Annette; Thorand, Barbara
• Is Part Of: Endocrine connections. Volume 9:Issue 4(2020)
• Page Start: 326
• Page End: 336
• Publication Date: 2020-04
• Subjects: SHBG -- testosterone -- DHT -- androgens -- mortality; Endocrinology -- Periodicals; 616.4005
• DOI: 10.1530/EC-20-0080
• Languages: English
• ISSNs: 2049-3614

Abstract

Abstract : Objective: Sex hormone-binding globulin (SHBG) and androgens have been associated with mortality in women and men, but controversy still exists. Our objective was to investigate associations of SHBG and androgens with all-cause and cause-specific mortality in men and women. Design: 1006 men and 709 peri- and postmenopausal women (age range: 45–82 years) from the German population-based KORA F4 cohort study were followed-up for a median of 8.7 years. Methods: SHBG was measured with an immunoassay, total testosterone (TT) and dihydrotestosterone (DHT) with mass-spectrometry in serum samples and we calculated free testosterone (cFT). To assess associations between SHBG and androgen levels and mortality, we calculated hazard ratios (HRs) with 95% CIs using Cox proportional-hazards models. Results: In the cohort, 128 men (12.7%) and 70 women (9.9%) died. In women, we observed positive associations of SHBG with all-cause (HR: 1.54, 95% CI: 1.16–2.04) and with other disease-related mortality (HR: 1.86, 95% CI: 1.08–3.20) and for DHT with all-cause mortality (HR: 1.32, 95% CI: 1.00–1.73). In men, we found a positive association of SHBG (HR: 1.24 95% CI: 1.00–1.54) and inverse associations of TT (HR: 0.87, 95% CI: 0.77–0.97) and cFT (HR: 0.84, 95% CI: 0.73–0.97) with all-cause mortality. No other associations were found for cause-specific mortality. Conclusions: Higher SHBG levels were associated with increased risk of all-cause mortality in men and women. Lower TT and cFT levels in men and higher DHT levels in women were associated with increased risk of all-cause mortality. Future, well-powered population-based studies should further investigate cause-specific mortality risk.