Postmenopausal women will be given either 3 weeks of oral 50 mg DHEA or placebo followed by a washout period and then a crossover into the opposite study arm. Insulin sensitivity will be determined by intravenous tolbutamide-augmented glucose tolerance test. Tissue sensitivity to insulin action will be determined by measuring in vitro red blood cell insulin binding.

Project Start
Project End
Budget Start
Budget End
Support Year
32
Fiscal Year
1996
Total Cost
Indirect Cost
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