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Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania

OBJECTIVE: The aim of this analysis was to assess the prospective association of serum testosterone and dehydroepiandrosterone sulfate (DHEAS) levels with incident metabolic syndrome (MetS) in men. RESEARCH DESIGN AND METHODS: Data were obtained from the Study of Health in Pomerania (SHIP), a popula...

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Autores principales: Haring, Robin, Völzke, Henry, Felix, Stephan B., Schipf, Sabine, Dörr, Marcus, Rosskopf, Dieter, Nauck, Matthias, Schöfl, Christof, Wallaschofski, Henri
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731522/
https://www.ncbi.nlm.nih.gov/pubmed/19581420
http://dx.doi.org/10.2337/db09-0031
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author Haring, Robin
Völzke, Henry
Felix, Stephan B.
Schipf, Sabine
Dörr, Marcus
Rosskopf, Dieter
Nauck, Matthias
Schöfl, Christof
Wallaschofski, Henri
author_facet Haring, Robin
Völzke, Henry
Felix, Stephan B.
Schipf, Sabine
Dörr, Marcus
Rosskopf, Dieter
Nauck, Matthias
Schöfl, Christof
Wallaschofski, Henri
author_sort Haring, Robin
collection PubMed
description OBJECTIVE: The aim of this analysis was to assess the prospective association of serum testosterone and dehydroepiandrosterone sulfate (DHEAS) levels with incident metabolic syndrome (MetS) in men. RESEARCH DESIGN AND METHODS: Data were obtained from the Study of Health in Pomerania (SHIP), a population-based prospective cohort of adults aged 20–79 years. Analyses were conducted in 1,004 men without baseline MetS defined by National Cholesterol Education Program Adult Treatment Panel III guidelines. Testosterone and DHEAS were categorized by age-specific quartiles and Poisson regression models with relative risks (RRs) and 95% CIs were estimated. RESULTS: After a median follow-up time of 5.0 years, 480 men (47.8%) developed MetS. Testosterone levels decreased with increasing number of MetS components. Testosterone in the lowest quartile predicted MetS (RR 1.38 [95% CI 1.13–1.69]), particularly among men aged 20–39 years (2.06 [1.29–3.29]), even after adjustment for age, smoking, alcohol consumption, physical activity, waist circumference, self-related health, and time of blood sampling. DHEAS levels were not related to incident MetS (0.99 [0.83–1.19]). CONCLUSIONS: Low testosterone but not DHEAS predicts development of MetS in a population-based cohort of 1,004 men aged 20–79 years. Especially in young men aged 20–39 years, results suggest low testosterone as a strong predictor for incident MetS. Assessment of testosterone in young and middle-age men may allow early interventions in the general population.
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spelling pubmed-27315222010-09-01 Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania Haring, Robin Völzke, Henry Felix, Stephan B. Schipf, Sabine Dörr, Marcus Rosskopf, Dieter Nauck, Matthias Schöfl, Christof Wallaschofski, Henri Diabetes Original Article OBJECTIVE: The aim of this analysis was to assess the prospective association of serum testosterone and dehydroepiandrosterone sulfate (DHEAS) levels with incident metabolic syndrome (MetS) in men. RESEARCH DESIGN AND METHODS: Data were obtained from the Study of Health in Pomerania (SHIP), a population-based prospective cohort of adults aged 20–79 years. Analyses were conducted in 1,004 men without baseline MetS defined by National Cholesterol Education Program Adult Treatment Panel III guidelines. Testosterone and DHEAS were categorized by age-specific quartiles and Poisson regression models with relative risks (RRs) and 95% CIs were estimated. RESULTS: After a median follow-up time of 5.0 years, 480 men (47.8%) developed MetS. Testosterone levels decreased with increasing number of MetS components. Testosterone in the lowest quartile predicted MetS (RR 1.38 [95% CI 1.13–1.69]), particularly among men aged 20–39 years (2.06 [1.29–3.29]), even after adjustment for age, smoking, alcohol consumption, physical activity, waist circumference, self-related health, and time of blood sampling. DHEAS levels were not related to incident MetS (0.99 [0.83–1.19]). CONCLUSIONS: Low testosterone but not DHEAS predicts development of MetS in a population-based cohort of 1,004 men aged 20–79 years. Especially in young men aged 20–39 years, results suggest low testosterone as a strong predictor for incident MetS. Assessment of testosterone in young and middle-age men may allow early interventions in the general population. American Diabetes Association 2009-09 2009-07-06 /pmc/articles/PMC2731522/ /pubmed/19581420 http://dx.doi.org/10.2337/db09-0031 Text en © 2009 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Article
Haring, Robin
Völzke, Henry
Felix, Stephan B.
Schipf, Sabine
Dörr, Marcus
Rosskopf, Dieter
Nauck, Matthias
Schöfl, Christof
Wallaschofski, Henri
Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania
title Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania
title_full Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania
title_fullStr Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania
title_full_unstemmed Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania
title_short Prediction of Metabolic Syndrome by Low Serum Testosterone Levels in Men: Results From the Study of Health in Pomerania
title_sort prediction of metabolic syndrome by low serum testosterone levels in men: results from the study of health in pomerania
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731522/
https://www.ncbi.nlm.nih.gov/pubmed/19581420
http://dx.doi.org/10.2337/db09-0031
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