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Changes over 14 years in androgenicity and body mass index in a biracial cohort of reproductive-age women

  • Barbara Sternfeld
  • , Kiang Liu
  • , Charles P. Quesenberry
  • , Hua Wang
  • , Sheng Fang Jiang
  • , Martha Daviglus
  • , Myriam Fornage
  • , Cora E. Lewis
  • , John Mahan
  • , Pamela J. Schreiner
  • , Stephen M. Schwartz
  • , Stephen Sidney
  • , O. Dale Williams
  • , David S. Siscovick

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Body mass index (BMI) is directly related to testosterone (total T and free T) and inversely to SHBG cross-sectionally, but little is known about how changes in body fat and androgen markers affect each other over time. Methods: Participants included 969 White and Black women from the Coronary Artery Risk Development in Young Adults (CARDIA) cohort, who were ages 18-30 at entry into the study and were pre- or perimenopausal 16 yr later at the time of the CARDIA Women's Study (CWS). Total T and SHBG were assayed from specimens drawn at the CWS examination and stored serum from the yr 2 and 10 CARDIA exams. Free T was calculated based on total T and SHBG. BMI and waist circumference were measured at yr 2, 10, and 16. Results: Despite clinically significant increases in BMI and waist circumference, total T and free T tended to decline, whereas SHBG remained relatively constant. BMI and waist circumference were directly correlated with free T and inversely correlated with SHBG in cross-sectional analyses. In longitudinal, multivariable analyses, an annualized increase in BMI was inversely related to a concurrent annualized decrease in SHBG (β = -0.79 ng/dl, and SE = 0.22 in Blacks; β = -1.07 ng/dl; and SE = 0.31 in Whites). However, early increases in BMI were not related to later decreases in SHBG. Conclusion: Increases in adiposity are closely tied to decreases in SHBG, but changes in BMI and SHBG may occur concurrently rather than sequentially.

Original languageEnglish (US)
Pages (from-to)2158-2165
Number of pages8
JournalJournal of Clinical Endocrinology and Metabolism
Volume93
Issue number6
DOIs
StatePublished - Jun 2008

Bibliographical note

Funding Information:
This research was supported by a grant from the National Heart, Lung, and Blood Institute (R01-HL065611) and contracts N01-HC-48047, N01-HC-48048, N01-HC-48049, and N01-HC-48050.

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