Sex steroids and cardiovascular disease

As men grow older, testosterone (T) levels decline and the significance of this change is debated. The evidence supporting a causal role for lower circulating T, or its metabolites dihydrotestosterone (DHT) and estradiol, in the genesis of atherosclerosis and cardiovascular disease (CVD) in men is l...

Full description

Bibliographic Details
Main Author: Bu Beng Yeap
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-04-01
Series:Asian Journal of Andrology
Subjects:
Online Access:http://www.ajandrology.com/article.asp?issn=1008-682X;year=2014;volume=16;issue=2;spage=239;epage=247;aulast=Yeap
id doaj-452648f1ab6b450bb6209b9a237f9cbb
record_format Article
spelling doaj-452648f1ab6b450bb6209b9a237f9cbb2020-11-24T23:15:48ZengWolters Kluwer Medknow PublicationsAsian Journal of Andrology1008-682X1745-72622014-04-0116223924710.4103/1008-682X.122357Sex steroids and cardiovascular diseaseBu Beng YeapAs men grow older, testosterone (T) levels decline and the significance of this change is debated. The evidence supporting a causal role for lower circulating T, or its metabolites dihydrotestosterone (DHT) and estradiol, in the genesis of atherosclerosis and cardiovascular disease (CVD) in men is limited. Observational studies associate low baseline T levels with carotid atherosclerosis, aortic and peripheral vascular disease, and with the incidence of cardiovascular events and mortality. Studies using mass spectrometry suggest that when total T is assayed optimally, calculation of free T might not necessarily improve risk stratification. There is limited evidence to support an association of estradiol with CVD. Interventional studies of T therapy in men with coronary artery disease have shown beneficial effects on exercise-induced myocardial ischemia. However, placebo-controlled, randomized clinical trials (RCTs) of T therapy in men with the prespecified outcomes of cardiovascular events or deaths are lacking. Meta-analyses of randomized controlled trials of T published up to 2010 found no increase in cardiovascular events, mortality, or prostate cancer with therapy. Recently, in a trial of older men with mobility limitations, men randomized to receive a substantial dose of T reported cardiovascular adverse effects. This phenomenon was not reported from a comparable trial where men received a more conservative dose of T, suggesting a prudent approach should be adopted when considering therapy in frail older men with existing CVD. Adequately powered RCTs of T in middle-aged and older men are needed to clarify whether or not hormonal intervention would reduce the incidence of CVD.http://www.ajandrology.com/article.asp?issn=1008-682X;year=2014;volume=16;issue=2;spage=239;epage=247;aulast=Yeapatherosclerosis; cardiovascular disease; dihydrotestosterone; estradiol; mortality; testosterone
collection DOAJ
language English
format Article
sources DOAJ
author Bu Beng Yeap
spellingShingle Bu Beng Yeap
Sex steroids and cardiovascular disease
Asian Journal of Andrology
atherosclerosis; cardiovascular disease; dihydrotestosterone; estradiol; mortality; testosterone
author_facet Bu Beng Yeap
author_sort Bu Beng Yeap
title Sex steroids and cardiovascular disease
title_short Sex steroids and cardiovascular disease
title_full Sex steroids and cardiovascular disease
title_fullStr Sex steroids and cardiovascular disease
title_full_unstemmed Sex steroids and cardiovascular disease
title_sort sex steroids and cardiovascular disease
publisher Wolters Kluwer Medknow Publications
series Asian Journal of Andrology
issn 1008-682X
1745-7262
publishDate 2014-04-01
description As men grow older, testosterone (T) levels decline and the significance of this change is debated. The evidence supporting a causal role for lower circulating T, or its metabolites dihydrotestosterone (DHT) and estradiol, in the genesis of atherosclerosis and cardiovascular disease (CVD) in men is limited. Observational studies associate low baseline T levels with carotid atherosclerosis, aortic and peripheral vascular disease, and with the incidence of cardiovascular events and mortality. Studies using mass spectrometry suggest that when total T is assayed optimally, calculation of free T might not necessarily improve risk stratification. There is limited evidence to support an association of estradiol with CVD. Interventional studies of T therapy in men with coronary artery disease have shown beneficial effects on exercise-induced myocardial ischemia. However, placebo-controlled, randomized clinical trials (RCTs) of T therapy in men with the prespecified outcomes of cardiovascular events or deaths are lacking. Meta-analyses of randomized controlled trials of T published up to 2010 found no increase in cardiovascular events, mortality, or prostate cancer with therapy. Recently, in a trial of older men with mobility limitations, men randomized to receive a substantial dose of T reported cardiovascular adverse effects. This phenomenon was not reported from a comparable trial where men received a more conservative dose of T, suggesting a prudent approach should be adopted when considering therapy in frail older men with existing CVD. Adequately powered RCTs of T in middle-aged and older men are needed to clarify whether or not hormonal intervention would reduce the incidence of CVD.
topic atherosclerosis; cardiovascular disease; dihydrotestosterone; estradiol; mortality; testosterone
url http://www.ajandrology.com/article.asp?issn=1008-682X;year=2014;volume=16;issue=2;spage=239;epage=247;aulast=Yeap
work_keys_str_mv AT bubengyeap sexsteroidsandcardiovasculardisease
_version_ 1725589580441190400