R
R. E. Van Pelt
Researcher at Anschutz Medical Campus
Publications - 10
Citations - 662
R. E. Van Pelt is an academic researcher from Anschutz Medical Campus. The author has contributed to research in topics: Insulin resistance & Insulin. The author has an hindex of 9, co-authored 10 publications receiving 630 citations. Previous affiliations of R. E. Van Pelt include Washington University in St. Louis & University of Colorado Denver.
Papers
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Journal ArticleDOI
Contributions of total and regional fat mass to risk for cardiovascular disease in older women.
TL;DR: T trunk fat is a strong independent predictor of insulin resistance and dyslipidemia in postmenopausal women, whereas leg fat appears to confer protective effects against metabolic dysfunction.
Journal ArticleDOI
Lower-body adiposity and metabolic protection in postmenopausal women
R. E. Van Pelt,Catherine M. Jankowski,Wendolyn S. Gozansky,Robert S. Schwartz,Wendy M. Kohrt +4 more
TL;DR: The finding that regional adipose tissue depots have apparent independent and opposing effects on serum TG supports the need for further research into the physiological mechanisms governing these effects.
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Waist circumference vs body mass index for prediction of disease risk in postmenopausal women
TL;DR: Waist circumference, an easily obtained index of central adiposity, is a more sensitive measure of relative disease risk than is BMI in middle-aged and older women, particularly in normal-weight individuals.
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Intravenous estrogens increase insulin clearance and action in postmenopausal women.
TL;DR: It is suggested that acute CE administration increases insulin clearance and action in postmenopausal women and reduces insulin action in women not using hormone replacement.
Journal ArticleDOI
Protection of Bone Mass by Estrogens and Raloxifene during Exercise-Induced Weight Loss
Wendolyn S. Gozansky,R. E. Van Pelt,Catherine M. Jankowski,Robert S. Schwartz,Wendy M. Kohrt +4 more
TL;DR: It is suggested that weight loss, even when modest in magnitude and induced by exercise training, causes a reduction in BMD, particularly in women not taking raloxifene or HT.