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Higher Serum Sex Hormone-Binding Globulin Levels Are Associated With Incident Cardiovascular Disease in Men
Prabin Gyawali1,2,3, Sean A Martin1,2,3, Leonie K Heilbronn1,3
1Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia.
Insights
Higher sex hormone-binding globulin (SHBG) and lower total testosterone (TT) are linked to increased cardiovascular disease (CVD) risk in men. This association was observed for incident CVD and, in older men, for CVD mortality.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Gerontology
Background:
- Sex hormone-binding globulin (SHBG) is linked to cardiovascular disease (CVD) risk factors.
- Prospective data on SHBG and CVD events are limited and conflicting.
Purpose of the Study:
- To investigate the association between serum SHBG, total testosterone (TT), and incident CVD.
- To examine the relationship between serum SHBG, TT, and CVD-related mortality in middle-aged to elderly men.
Main Methods:
- Analysis of 1492 men (35-80 years) from the Men Androgen Inflammation Lifestyle Environment and Stress cohort.
- Logistic regression and Cox proportional hazard models were used to assess associations, adjusting for CVD risk factors.
Main Results:
- Elevated SHBG and lower TT were independently associated with incident CVD.
- A decrease in TT over time also correlated with increased CVD risk.
- SHBG and TT were not significantly associated with all-age CVD mortality.
Conclusions:
- In middle-aged and elderly men, higher SHBG and lower TT are independently associated with a greater risk of incident CVD.
- In men over 65, these hormonal factors are also linked to increased CVD mortality risk.
Context:
Sex hormone-binding globulin (SHBG) levels are associated with cardiovascular disease (CVD) risk factors. However, prospective data on the association between SHBG levels and CVD events are sparse, with conflicting results.
Objectives:
To examine associations between serum SHBG, total testosterone (TT), and incident CVD and CVD-related mortality in middle-aged to elderly men.
Design And Methods:
Data on 2563 community-dwelling men (35 to 80 years) were obtained from participants in the Men Androgen Inflammation Lifestyle Environment and Stress cohort. The analytic sample included 1492 men without baseline (2002 to 2007) CVD and with fasted morning serum SHBG and TT available at both baseline and follow-up (2007 to 2010) and without medications affecting TT or SHBG. Associations of baseline SHBG and TT, with incident CVD and CVD mortality, were analyzed using logistic regression for incident CVD and Cox proportional hazard regression for CVD mortality, adjusting for established CVD risk factors.
Results:
In multivariable models, elevated baseline SHBG and lower baseline TT were independently associated with incident CVD (SHBG: OR, 1.54; 95% CI, 1.15 to 2.06 per SD increase in SHBG, P = 0.003; TT: OR, 0.71; 95% CI, 0.52 to 0.97 per SD decrease in TT; P = 0.03). A decrease in TT between time points was associated with incident CVD (OR, 0.72; 95% CI, 0.56 to 0.92; P = 0.01). Neither SHBG nor TT was significantly associated with all-age CVD mortality [hazard ratio (HR), 0.69; 95% CI, 0.29 to 1.63; P = 0.40; and HR, 0.60; 95% CI, 0.28 to 1.26; P = 0.18, respectively].
Conclusions:
Among all men and men >65 years, elevated SHBG and lower TT were independently associated with both a greater risk of CVD and an increased CVD mortality risk.
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