The effect of estradiol and a combined estradiol progestagen preparation on insulin sensitivity in healthy postmenopausal women

被引:59
作者
Duncan, AC
Lyall, H
Roberts, RN
Petrie, JR
Perera, MJ
Monaghan, S
Hart, DM
Connell, JMC
Lumsden, MA
机构
[1] Queen Mothers Hosp, Dept Obstet & Gynecol, Glasgow G3 8SJ, Lanark, Scotland
[2] Western Infirm & Associated Hosp, Dept Med & Therapeut, Glasgow G11 8NT, Lanark, Scotland
关键词
D O I
10.1210/jc.84.7.2402
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Abnormalities of carbohydrate metabolism and insulin sensitivity have been reported in estrogen deficiency. Estrogen replacement appears to result in an improvement in these parameters, although progestagens may antagonize these effects. We have examined the effects of transdermal estradiol and oral norethisterone on insulin sensitivity using the hyperinsulinemic euglycemic clamp method by performing a randomized, double blind, placebo-controlled study in 22 healthy women after a surgically induced menopause. After baseline measurements, subjects were randomized to receive either transdermal 17 beta-estradiol (50 mu g) or matching placebo patches for 6 weeks. The subjects were then further randomized to receive either estradiol in combination with oral norethisterone (1 mg) or a matching oral placebo preparation, crossing over after 6 weeks, with assessment insulin sensitivity at the end of each treatment. No significant increase in insulin sensitivity was observed after 6 weeks of transdermal 17 beta-estradiol treatment (95% confidence interval, -0.54, 1.86; P = 0.27). Addition of norethisterone for a further 6 weeks had no detectable effect on insulin sensitivity (95% confidence interval, -1.65, 1.10; P = 0.65). The results of this study using transdermal estradiol do not support previous reports that unopposed estrogens exert potentially beneficial effects on insulin sensitivity and suggest that the addition of an oral progestagen confers no clinically important risk or benefit. It is therefore unlikely that effects on insulin sensitivity contribute appreciably to the cardioprotective benefits attributed to hormone replacement therapy.
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页码:2402 / 2407
页数:6
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