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Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men

As men grow older, circulating testosterone declines while the incidence of cardiovascular disease increases. Thus, the role of sex hormones as biomarkers, and possibly contributing factors to clinical manifestations of cardiovascular disease in the increasing demographic of aging men, has attracted...

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Autor principal: Yeap, Bu B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858092/
https://www.ncbi.nlm.nih.gov/pubmed/29199649
http://dx.doi.org/10.4103/aja.aja_50_17
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author Yeap, Bu B
author_facet Yeap, Bu B
author_sort Yeap, Bu B
collection PubMed
description As men grow older, circulating testosterone declines while the incidence of cardiovascular disease increases. Thus, the role of sex hormones as biomarkers, and possibly contributing factors to clinical manifestations of cardiovascular disease in the increasing demographic of aging men, has attracted considerable interest. This review focuses on observational studies of endogenous androgens, namely circulating testosterone and dihydrotestosterone, which have examined their associations with cardiovascular events such as myocardial infarction and stroke. Studies which have examined the associations of endogenous estrogens, namely circulating estradiol, with these outcomes are also discussed. In large prospective cohort studies of predominantly middle-aged and older men, lower circulating testosterone consistently predicts higher incidence of cardiovascular events. Of note, both lower circulating testosterone and lower dihydrotestosterone are associated with higher incidence of stroke. These associations are less apparent when myocardial infarction is considered as the outcome. Results for estradiol are inconsistent. Lower circulating testosterone has been shown to predict higher cardiovascular disease-related mortality, as has lower circulating dihydrotestosterone. It is possible that the relationship of circulating androgens to cardiovascular events or mortality outcomes may be U-shaped rather than linear, with an optimal range defining men at lowest risk. Epidemiological studies are observational in nature and do not prove causality. Associations observed in studies of endogenous androgens need not necessarily translate into similar effects of exogenous androgens. Rigorous randomized controlled trials are needed to clarify the effects of testosterone treatment on cardiovascular risk in men.
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spelling pubmed-58580922018-03-23 Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men Yeap, Bu B Asian J Androl Invited Review As men grow older, circulating testosterone declines while the incidence of cardiovascular disease increases. Thus, the role of sex hormones as biomarkers, and possibly contributing factors to clinical manifestations of cardiovascular disease in the increasing demographic of aging men, has attracted considerable interest. This review focuses on observational studies of endogenous androgens, namely circulating testosterone and dihydrotestosterone, which have examined their associations with cardiovascular events such as myocardial infarction and stroke. Studies which have examined the associations of endogenous estrogens, namely circulating estradiol, with these outcomes are also discussed. In large prospective cohort studies of predominantly middle-aged and older men, lower circulating testosterone consistently predicts higher incidence of cardiovascular events. Of note, both lower circulating testosterone and lower dihydrotestosterone are associated with higher incidence of stroke. These associations are less apparent when myocardial infarction is considered as the outcome. Results for estradiol are inconsistent. Lower circulating testosterone has been shown to predict higher cardiovascular disease-related mortality, as has lower circulating dihydrotestosterone. It is possible that the relationship of circulating androgens to cardiovascular events or mortality outcomes may be U-shaped rather than linear, with an optimal range defining men at lowest risk. Epidemiological studies are observational in nature and do not prove causality. Associations observed in studies of endogenous androgens need not necessarily translate into similar effects of exogenous androgens. Rigorous randomized controlled trials are needed to clarify the effects of testosterone treatment on cardiovascular risk in men. Medknow Publications & Media Pvt Ltd 2018 2017-12-01 /pmc/articles/PMC5858092/ /pubmed/29199649 http://dx.doi.org/10.4103/aja.aja_50_17 Text en Copyright: © The Author(s)(2018) http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Invited Review
Yeap, Bu B
Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
title Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
title_full Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
title_fullStr Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
title_full_unstemmed Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
title_short Testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
title_sort testosterone and its metabolites: differential associations with cardiovascular and cerebrovascular events in men
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858092/
https://www.ncbi.nlm.nih.gov/pubmed/29199649
http://dx.doi.org/10.4103/aja.aja_50_17
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