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Published on: December 10, 2013
Endogenous sex hormones and cardiovascular disease incidence in men
Johan Arnlöv1, Michael J Pencina, Shreyasee Amin
1National Heart, Lung, and Blood Institute's Framingham Heart Study, National Institutes of Health, Bethesda, Maryland, USA.
Higher estradiol levels were linked to reduced cardiovascular disease (CVD) risk in older men. This suggests a potential protective role for estrogen in men
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Epidemiology
Background:
- Endogenous sex hormones (testosterone, DHEA-S, estradiol) may influence cardiovascular disease (CVD) risk factors and vascular function.
- Previous studies on sex hormones and CVD incidence in men have produced conflicting results.
Purpose of the Study:
- To investigate the relationship between circulating sex hormone levels and the risk of developing CVD in men.
- To determine if estradiol, testosterone, or dehydroepiandrosterone sulfate (DHEA-S) levels are associated with incident CVD.
Main Methods:
- A prospective cohort study was conducted with 2084 middle-aged white men without baseline CVD.
- Multivariable Cox regression analysis was used to assess the association between baseline hormone levels (testosterone, DHEA-S, estradiol) and CVD incidence over 10 years.
- CVD outcomes included coronary, cerebrovascular, peripheral vascular disease, and heart failure.
Main Results:
- Higher serum estradiol levels were associated with a significantly lower risk of CVD events (HR per SD increment, 0.90; P = 0.035).
- This association was more pronounced in older men (median age >56 years) (HR per SD increment, 0.86; P = 0.005).
- Serum testosterone and DHEA-S levels showed no significant association with incident CVD.
Conclusions:
- Elevated serum estradiol levels are associated with a reduced risk of cardiovascular disease in older men.
- These findings support the hypothesis that endogenous estrogen may exert vasculoprotective effects in men.
- Limitations include baseline hormone measurements and potential lack of generalizability to women and nonwhite populations.
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