1. ^*Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, and Harvard Medical School, Boston, Massachusetts
2. ^†Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts
3. ^‡Division of Endocrinology, Diabetes, & Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts

Correspondence: Shelley S. Tworoger Channing Laboratory, 181 Longwood Ave., 3rd Floor, Boston, MA 02115. E-mail: nhsst@channing.harvard.edu

^*The costs of publication of this article were defrayed, in part, by the payment of page charges. This article must, therefore, be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received 29 November 2006; Revised  0000; Accepted 29 January 2007.

Abstract

Objective: Recent studies have suggested that a relationship between adiponectin and sex hormone, prolactin, and insulin-like growth factor levels could be important for breast cancer risk and insulin sensitivity. Therefore, we assessed the relationship of adiponectin with plasma concentrations of estrone; estradiol; estrone sulfate; testosterone; androstenedione; dehydroepiandrosterone (DHEA); dehydroepiandrosterone sulfate (DHEAS); sex hormone binding globulin (SHBG); prolactin; insulin-like growth factor (IGF-1); its binding protein, IGF binding protein 3 (IGFBP-3); c-peptide; and IGF binding protein 1 (IGFBP-1) among 360 postmenopausal women not taking postmenopausal hormones from the Nurses' Health Study.

Research Methods and Procedures: Multivariate models were adjusted for physical activity, alcohol consumption, age at blood draw, age at first birth/parity, fasting status, and time of day of blood draw; a separate model was additionally adjusted for BMI at blood draw.

Results: Estrogens were inversely associated with adiponectin levels; however, except for free estradiol, these associations were substantially attenuated after adjustment for BMI. Free estradiol levels were 27% lower among women in the top vs. bottom quartile of adiponectin levels. No consistent associations were observed for the androgens, prolactin, IGF-1, and IGFBP-3. However, SHBG, c-peptide, and IGFBP-1 were strongly and independently associated with adiponectin levels (r = 0.29, - 0.30, 0.24, respectively).

Conclusion: With the exceptions of SHBG, c-peptide, and IGFBP-1, the studied analytes were modestly associated with adiponectin and the associations were, in large part, mediated by body fat.