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口服雌酮与17β-雌二醇对绝经后女性脂蛋白的不同影响。

Differential effects of oral estrone versus 17 beta-estradiol on lipoproteins in postmenopausal women.

作者信息

Colvin P L, Auerbach B J, Koritnik D R, Hazzard W R, Applebaum-Bowden D

机构信息

Department of Internal Medicine, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27103.

出版信息

J Clin Endocrinol Metab. 1990 Jun;70(6):1568-73. doi: 10.1210/jcem-70-6-1568.

DOI:10.1210/jcem-70-6-1568
PMID:2347894
Abstract

Toward the definition of optimal postmenopausal estrogen replacement we compared the effects of three graduated doses of two oral estrogens, estrone sulfate and 17 beta-estradiol, on the lipid profiles of two groups of six postmenopausal women. Because of metabolic interconversions equivalent serum concentrations of estrone and estradiol were produced with these regimens. However, differential effects were noted in lipoproteins. 17 beta-Estradiol caused an increase in total plasma cholesterol (from 5.71 +/- 0.36 to 5.99 +/- 0.57 mmol/L, baseline to high dose; P less than 0.02), high density lipoprotein (HDL) cholesterol (from 1.45 +/- 0.15 to 1.78 +/- 0.36 mmol/L; P less than 0.02), HDL2 cholesterol concentration (from 0.41 +/- 0.08 to 0.62 +/- 0.26 mmol/L; P less than 0.01), and triglyceride concentration (from 1.09 +/- 0.29 to 1.24 +/- 0.30 mmol/L; P less than 0.01) without affecting low density lipoprotein (LDL) cholesterol concentration. By contrast, estrone sulfate caused a decrease in total plasma cholesterol (from 6.51 +/- 0.85 to 5.87 +/- 0.41 mmol/L; P less than 0.05) and LDL cholesterol concentration (from 4.34 +/- 0.57 to 3.67 +/- 0.44 mmol/L; P less than 0.01) and an increase in HDL cholesterol (from 1.37 +/- 0.20 to 1.50 +/- 0.26 mmol/L; P less than 0.05) and HDL2 cholesterol concentration (from 0.34 +/- 0.18 to 0.49 +/- 0.18 mmol/L; P less than 0.01), but no change in total triglyceride concentration. We deduce that the differential effect of orally administered estrogens on lipoprotein metabolism in postmenopausal women may be attributed to a first pass effect on hepatic metabolism.

摘要

为了明确绝经后雌激素替代治疗的最佳方案,我们比较了两种口服雌激素(硫酸雌酮和17β - 雌二醇)的三种递增剂量对两组各六名绝经后女性血脂谱的影响。由于代谢转化,这些方案产生了等效血清浓度的雌酮和雌二醇。然而,在脂蛋白方面观察到了不同的影响。17β - 雌二醇使总血浆胆固醇升高(从基线时的5.71±0.36 mmol/L升至高剂量时的5.99±0.57 mmol/L;P<0.02),高密度脂蛋白(HDL)胆固醇升高(从1.45±0.15 mmol/L升至1.78±0.36 mmol/L;P<0.02),HDL2胆固醇浓度升高(从0.41±0.08 mmol/L升至0.62±0.26 mmol/L;P<0.01),甘油三酯浓度升高(从1.09±0.29 mmol/L升至1.24±0.30 mmol/L;P<0.01),而低密度脂蛋白(LDL)胆固醇浓度未受影响。相比之下,硫酸雌酮使总血浆胆固醇降低(从6.51±0.85 mmol/L降至5.87±0.41 mmol/L;P<0.05),LDL胆固醇浓度降低(从4.34±0.57 mmol/L降至3.67±0.44 mmol/L;P<0.01),HDL胆固醇升高(从1.37±0.20 mmol/L升至1.50±0.26 mmol/L;P<0.05),HDL2胆固醇浓度升高(从0.34±0.18 mmol/L升至0.49±0.18 mmol/L;P<0.01),但总甘油三酯浓度无变化。我们推断,口服雌激素对绝经后女性脂蛋白代谢的不同影响可能归因于对肝脏代谢的首过效应。

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Differential effects of oral estrone versus 17 beta-estradiol on lipoproteins in postmenopausal women.口服雌酮与17β-雌二醇对绝经后女性脂蛋白的不同影响。
J Clin Endocrinol Metab. 1990 Jun;70(6):1568-73. doi: 10.1210/jcem-70-6-1568.
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Effects of postmenopausal estrogen replacement on the concentrations and metabolism of plasma lipoproteins.绝经后雌激素替代疗法对血浆脂蛋白浓度及代谢的影响。
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Oral but not transdermal estrogen replacement therapy changes the composition of plasma lipoproteins.口服而非经皮雌激素替代疗法会改变血浆脂蛋白的组成。
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Oral contraceptive and postmenopausal estrogen effects on lipoprotein triglyceride and cholesterol in an adult female population: relationships to estrogen and progestin potency.口服避孕药和绝经后雌激素对成年女性人群脂蛋白甘油三酯和胆固醇的影响:与雌激素和孕激素效力的关系。
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Serum lipid profile improved by ultra-low doses of 17 beta-estradiol in elderly women.超低剂量17β-雌二醇可改善老年女性的血脂状况。
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[Plasma levels of total cholesterol, LDL-cholesterol, and HDL-cholesterol in postmenopausal women during 12 months' oral administration of dydrogesterone or medroxyprogesterone combined with continuous transdermal supplementation of 17beta-estradiol].[绝经后女性口服地屈孕酮或甲羟孕酮联合持续经皮补充17β-雌二醇12个月期间的总胆固醇、低密度脂蛋白胆固醇和高密度脂蛋白胆固醇血浆水平]
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Differential lipemic and hormonal responses to oral and parenteral 17 beta-estradiol in postmenopausal women.绝经后女性对口服和肠胃外17β-雌二醇的血脂和激素反应差异。
Am J Obstet Gynecol. 1983 Sep 1;147(1):77-81. doi: 10.1016/0002-9378(83)90088-1.
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N Engl J Med. 1983 Apr 14;308(15):862-7. doi: 10.1056/NEJM198304143081502.

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