The Effect of Raloxifene on Glyco-Insulinemic Homeostasis in Healthy Postmenopausal Women: A Randomized Placebo-Controlled Study
Francesco Cucinelli,
Liberato Soranna,
Daniela Romualdi,
Giuseppe Muzj,
Salvatore Mancuso and
Antonio Lanzone
Department of Obstetrics and Gynecology (F.C., D.R., G.M., S.M.), Catholic University of Sacred Heart, 00168 Rome, Italy; and OASI Institute for Research (L.S., A.L.), 94018 Troina (Enna), Italy
Address all correspondence and requests for reprints to: Antonio Lanzone, M.D., Department of Obstetrics and Gynecology, Catholic University of Sacred Heart, L. go A. Gemelli 8, 00168 Rome, Italy. E-mail: . alanzone{at}rm.unicatt.it
Abstract
The effect of raloxifene, a selective estrogen receptor modulatorrecently approved as a therapeutic agent for menopause, on glyco-insulinemicmetabolism was investigated in 40 healthy postmenopausal women.
At the baseline and after 12 wk of raloxifene (60 mg/d) or placeboadministration, all aspects of glucose metabolism were evaluatedin each subject using both an oral glucose tolerance test (OGTT;75 g) and a hyperinsulinemic euglycemic clamp to assess peripheralinsulin sensitivity. Glucose, insulin, and C-peptide, measuredin fasting conditions, as well as glucose and insulin responsesto OGTT [expressed as area under curve (AUC)] were not modifiedby raloxifene, whereas C-peptide-AUC increased significantly(P < 0.05). Furthermore, a trend toward an improvement ofperipheral insulin sensitivity and hepatic clearance of thehormone (fractional hepatic insulin extraction) was observedin the raloxifene-treated women with respect to the controlpatients. When the subjects were studied in relation to theirinsulin secretion in response to the glucose load, the patients,classified as hyperinsulinemic, showed the most significantresponse to the raloxifene treatment. In these women, the selectiveestrogen receptor modulator was able to induce a significantreduction of insulin circulating plasma values (P < 0.01)through both an increase of fractional hepatic insulin extraction(P < 0.01) and an improvement of the peripheral insulin sensitivity(P < 0.05). On the contrary, no net change of insulin dynamicswas observed in normoinsulinemic and placebo-treated women.
The present data indicate that raloxifene does not negativelyinfluence glyco-insulinemic metabolism in unselected postmenopausalwomen and may indeed improve the excessive insulin responsivenessto OGTT in a selected population of hyperinsulinemic postmenopausalwomen.
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