Effects of metformin and leuprolide acetate on insulin resistance and testosterone levels in nondiabetic postmenopausal women: a randomized, placebo-controlled trial
Objective
To determine whether insulin sensitizers lower androgen levels and whether androgen suppression improves insulin resistance in nondiabetic postmenopausal women.
Design
Randomized, double-blind, placebo-controlled study.
Setting
Clinical and Translational Research Center of a university hospital.
Patient(s)
Thirty-five postmenopausal women aged 50–79 years with insulin resistance and higher T levels.
Intervention(s)
Subjects were randomized to metformin plus leuprolide acetate (LA) placebo, LA plus metformin placebo, or LA placebo plus metformin placebo in a 1:1:1 fashion during a 12-week period.
Main Outcome Measure(s)
Insulin sensitivity (M) assessed by euglycemic–hyperinsulinemic clamp and free T by equilibrium dialysis.
Result(s)
In those randomized to metformin, free T decreased by 19% compared with placebo, along with an expected improvement in M. Total T also decreased significantly, whereas sex hormone-binding globulin (SHBG) did not change. In those randomized to LA, the percent change in M was not different from placebo, despite a 48% relative decrease in free T levels.
Conclusion(s)
These data are the first to establish a causal link between insulin resistance and T in postmenopausal women. They confirm that treatment of insulin resistance decreases T production in this population and demonstrate that pharmacologic lowering of T does not affect insulin resistance.
Key Words: Testosterone, insulin resistance, polycystic ovary syndrome, metabolic syndrome, aging, elderly, women
To access this article, please choose from the options below
S.M.P. has nothing to disclose. N.I. has nothing to disclose. S.K. has nothing to disclose. S.J.R. has nothing to disclose. M.R.R. has nothing to disclose. M.P.R. has nothing to disclose. T.S. has nothing to disclose. A.B. has nothing to disclose. C.F. has nothing to disclose. A.R.C. has nothing to disclose.
Supported by K23 AG19161 from the National Institute on Aging, UL1RR024134 from the National Center for Research Resources, P30 DK19525 from the National Institute of Diabetes and Digestive and Kidney Diseases, the John A. Hartford Foundation, and the University of Pennsylvania Institute for Diabetes, Obesity, and Metabolism. The views expressed are those of the authors and do not necessarily represent the official views of the National Institutes of Health.
PII: S0015-0282(10)00139-1
doi:10.1016/j.fertnstert.2010.01.064
© 2010 American Society for Reproductive Medicine. All rights reserved.

