Changes in Visceral Adiposity, Subcutaneous Adiposity, and Sex Hormones in the Diabetes Prevention Program

Publication Description
Context: The degree to which changes in visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) relate to corresponding changes in plasma sex steroids is not known. Objective: We examined whether changes in VAT and SAT areas assessed by computed tomography were associated with changes in sex hormones (dehydroepiandrosterone [DHEAS], testosterone, estradiol, estrone, and sex hormone binding globulin [SHBG]) among Diabetes Prevention Program participants. Design: Secondary analysis of a randomized trial. Participants: Overweight and glucose-intolerant men (n=246) and women (n=309). Interventions: Intensive lifestyle change with goals of weight reduction and 150 min/week of moderate intensity exercise or metformin administered 850 mg twice a day or placebo. Main Outcome Measures: Associations between changes in VAT, SAT and sex hormone changes over one year. Results: Among men, reductions in VAT and SAT were both independently associated with significant increases in total testosterone and SHBG in fully-adjusted models. Among women, reductions in VAT and SAT were both independently associated with increases in SHBG and associations with estrone differed by menopausal status. Associations were similar by race/ethnicity and by randomization arm. No significant associations were observed between change in fat depot with change in estradiol or DHEAS. Conclusions: Among overweight adults with impaired glucose intolerance, reductions in either VAT and SAT were associated with increased total testosterone in men and higher SHBG in men and women. Weight loss may affect sex hormone profiles via reductions in visceral and subcutaneous fat.

Primary Author
Kim,C.
Dabelea,D.
Kalyani,R. R.
Christophi,C. A.
Bray,G. A.
Pi-Sunyer,X.
Darwin,C. H.
Yalamanchi,S.
Barrett-Connor,E.
Golden,S. H.
Boyko,E. J.

Author Address
Departments of Medicine, Obstetrics & Gynecology, and Epidemiology, University of Michigan, Ann Arbor, MI.; Department of Epidemiology, University of Colorado, Denver, CO.; Department of Medicine, Johns Hopkins University, Baltimore, MD.; Biosta(TRUNCATED)

Author Address
Departments of Medicine, Obstetrics & Gynecology, and Epidemiology, University of Michigan, Ann Arbor, MI.; Department of Epidemiology, University of Colorado, Denver, CO.; Department of Medicine, Johns Hopkins University, Baltimore, MD.; Biosta(TRUNCATED)

PMID
28651370

PMCID
PMC5587076



Reference Type
Journal Article

Periodical Full
The Journal of clinical endocrinology and metabolism

Publication Year
2017

Publication Date
23-Jun

Place of Publication
United States

ISSN/ISBN
1945-7197

Document Object Index
10.1210/jc.2017-00967 [doi]

Accession Number
PMID: 28651370