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Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study

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...

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Autores principales: Schederecker, Florian, Cecil, Alexander, Prehn, Cornelia, Nano, Jana, Koenig, Wolfgang, Adamski, Jerzy, Zeller, Tanja, Peters, Annette, Thorand, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219137/
https://www.ncbi.nlm.nih.gov/pubmed/32168474
http://dx.doi.org/10.1530/EC-20-0080
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author Schederecker, Florian
Cecil, Alexander
Prehn, Cornelia
Nano, Jana
Koenig, Wolfgang
Adamski, Jerzy
Zeller, Tanja
Peters, Annette
Thorand, Barbara
author_facet Schederecker, Florian
Cecil, Alexander
Prehn, Cornelia
Nano, Jana
Koenig, Wolfgang
Adamski, Jerzy
Zeller, Tanja
Peters, Annette
Thorand, Barbara
author_sort Schederecker, Florian
collection PubMed
description 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.
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spelling pubmed-72191372020-05-18 Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study Schederecker, Florian Cecil, Alexander Prehn, Cornelia Nano, Jana Koenig, Wolfgang Adamski, Jerzy Zeller, Tanja Peters, Annette Thorand, Barbara Endocr Connect Research 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. Bioscientifica Ltd 2020-03-13 /pmc/articles/PMC7219137/ /pubmed/32168474 http://dx.doi.org/10.1530/EC-20-0080 Text en © 2020 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Schederecker, Florian
Cecil, Alexander
Prehn, Cornelia
Nano, Jana
Koenig, Wolfgang
Adamski, Jerzy
Zeller, Tanja
Peters, Annette
Thorand, Barbara
Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study
title Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study
title_full Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study
title_fullStr Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study
title_full_unstemmed Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study
title_short Sex hormone-binding globulin, androgens and mortality: the KORA-F4 cohort study
title_sort sex hormone-binding globulin, androgens and mortality: the kora-f4 cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7219137/
https://www.ncbi.nlm.nih.gov/pubmed/32168474
http://dx.doi.org/10.1530/EC-20-0080
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