首页> 外文期刊>Metabolism: Clinical and Experimental >Effects of oral and transdermal 17beta-estradiol with cyclical oral norethindrone acetate on insulin sensitivity, secretion, and elimination in postmenopausal women.
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Effects of oral and transdermal 17beta-estradiol with cyclical oral norethindrone acetate on insulin sensitivity, secretion, and elimination in postmenopausal women.

机译:口服和经皮17β-雌二醇与周期性口服醋酸炔诺酮对绝经后妇女胰岛素敏感性,分泌和清除的影响。

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摘要

Few studies have examined the effects of 17beta-estradiol on parameters of insulin and glucose metabolism. We studied 42 healthy, untreated postmenopausal women seeking relief from menopausal symptoms. They were randomized to receive either oral 17beta-estradiol 2 mg daily combined with sequential oral norethindrone acetate (NETA) 1 mg daily from days 12 to 22, or transdermal 17beta-estradiol 0.05 mg daily combined with sequential oral NETA 1 mg daily from days 17 to 28. Intravenous glucose tolerance tests (IVGTTs) were performed at baseline and after 46 weeks (estrogen-alone phase) and 48 weeks (combined phase) of completed therapy. Mathematical modeling analysis of plasma glucose, insulin, and C-peptide concentration profiles provided measures of insulin resistance, secretion, and elimination. Both types of therapy were associated with a decrease in fasting insulin and glucose levels. Insulin sensitivity was increased by oral estradiol during the estrogen-alone phase but was reversed by the addition of NETA. Transdermal estradiol did not affect insulin sensitivity. Hepatic insulin uptake and insulin secretion were increased with both types of treatment. The oral regimen of estradiol therapy was favorable to both insulin elimination and sensitivity. Transdermal estradiol therapy had relatively few effects on insulin metabolism.
机译:很少有研究检查17β-雌二醇对胰岛素和葡萄糖代谢参数的影响。我们研究了42位未接受治疗的健康绝经后妇女,她们希望从绝经期症状中缓解。从第12天到第22天,他们随机接受口服每天2 mg口服17β-雌二醇联合口服醋酸炔诺酮(NETA)每天1 mg,或从每天第17天开始每天口服经皮17beta-雌二醇0.05 mg联合口服NETA 1 mg 28至28.在基线水平以及完成治疗的46周(仅雌激素阶段)和48周(联合阶段)后进行静脉葡萄糖耐量测试(IVGTT)。血浆葡萄糖,胰岛素和C肽浓度分布的数学模型分析提供了胰岛素抵抗,分泌和清除的指标。两种疗法均与空腹胰岛素和葡萄糖水平降低有关。在雌激素单药阶段,口服雌二醇可提高胰岛素敏感性,但通过添加NETA可逆转胰岛素敏感性。透皮雌二醇不影响胰岛素敏感性。两种治疗方法均增加了肝脏的胰岛素吸收和胰岛素分泌。雌二醇治疗的口服方案有利于胰岛素的消除和敏感性。透皮雌二醇疗法对胰岛素代谢的影响相对较小。

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