Higher Serum Sex Hormone–Binding Globulin Levels Are Associated With Incident Cardiovascular Disease in Men

Author:

Gyawali Prabin123ORCID,Martin Sean A123,Heilbronn Leonie K13,Vincent Andrew D123,Jenkins Alicia J4,Januszewski Andrzej S4,Adams Robert J T5,O’Loughlin Peter D6,Wittert Gary A123

Affiliation:

1. Adelaide Medical School, University of Adelaide, Adelaide, South Australia, Australia

2. Freemasons Foundation Centre for Men’s Health, University of Adelaide, Adelaide, South Australia, Australia

3. South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia

4. National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown, New South Wales, Australia

5. Adelaide Institute for Sleep Health, Flinders University, Adelaide, South Australia, Australia

6. Chemical Pathology, SA Pathology, Adelaide, South Australia, Australia

Abstract

AbstractContextSex 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.ObjectivesTo examine associations between serum SHBG, total testosterone (TT), and incident CVD and CVD-related mortality in middle-aged to elderly men.Design and MethodsData 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.ResultsIn 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].ConclusionsAmong 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.

Funder

National Health and Medical Research Council

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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