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序贯联合经皮和口服激素替代疗法对绝经后妇女血清脂质和脂蛋白的影响。

Effects of sequential combined transdermal and oral hormone replacement therapies on serum lipid and lipoproteins in postmenopausal women.

作者信息

Sendag F, Karadadas N, Ozsener S, Bilgin O

机构信息

Department of Gynecology and Obstetrics, Ege University School of Medicine, Bornova, Izmir, Turkey.

出版信息

Arch Gynecol Obstet. 2002 Jan;266(1):38-43. doi: 10.1007/pl00007497.

Abstract

The aim of this study was to compare the effects of sequential combined transdermal and oral postmenopausal hormone replacement therapies on serum lipid-lipoprotein profiles risk markers for cardiovascular disease. A prospective randomize study was designed: Ninety-six healthy nonhysterectomised postmenopausal women were randomized to receive either transdermal continuous 17beta-estradiol, 0.05 mg/d (Estraderm TTS, Novartis, Basel, Switzerland), with transdermal sequential norethisterone acetate, 0.25 mg/d (Estragest TTS, Novartis, Basel, Switzerland), or oral continuous conjugated equine estrogens, 0.625 mg/d (Premarin 0.625 mg, Wyeth, Philadelphia, U.S.A.), with oral sequential medroxyprogesterone acetate, 10 mg/d (Farlutal 5 mg, Deva, Istanbul, Turkey). 84 women completed the trial, 42 in oral and 42 in the transdermal group. The serum levels of total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides, apolipoproteins AI and apolipoproteins B at 6 months after starting treatment were compared with baseline values for both therapies. Both oral and transdermal therapies significantly reduced serum levels of total cholesterol (208-190 mg/dL and 216-199 mg/dL, respectively, p=0.0001) and LDL-cholesterol (128-112 mg/dL and 140-127 mg/dL, respectively, p=0.001). The serum levels of triglycerides did not show any significant change with oral therapy, whereas this lipid fell (128-101 mg/dL, p=0.0001) significantly with transdermal therapy. We found significant decrease in HDL-cholesterol with transdermal therapy while there was no significant change with oral therapy. Apolipoproteins AI, the major protein component of HDL2 subfraction, was increased by oral therapy and lowered by transdermal therapy. As a conclusion, we have found that serum total cholesterol and LDL-cholesterol were lowered by both therapies, with no significant differences between treatments, whereas there were significant differences between treatments according to effects on serum triglycerides and apolipoproteins AI.

摘要

本研究的目的是比较序贯联合经皮和口服绝经后激素替代疗法对心血管疾病血清脂质 - 脂蛋白谱风险标志物的影响。设计了一项前瞻性随机研究:96名健康的未行子宫切除术的绝经后妇女被随机分为两组,一组接受经皮持续给予17β - 雌二醇,0.05 mg/d(Estraderm TTS,诺华公司,瑞士巴塞尔),同时经皮序贯给予醋酸炔诺酮,0.25 mg/d(Estragest TTS,诺华公司,瑞士巴塞尔);另一组接受口服持续给予结合马雌激素,0.625 mg/d(Premarin 0.625 mg,惠氏公司,美国费城),同时口服序贯给予醋酸甲羟孕酮,10 mg/d(Farlutal 5 mg,Deva公司,土耳其伊斯坦布尔)。84名女性完成了试验,口服组和经皮组各42名。比较了两种疗法开始治疗6个月后总胆固醇、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇、甘油三酯、载脂蛋白AI和载脂蛋白B的血清水平与基线值。口服和经皮疗法均显著降低了总胆固醇的血清水平(分别为208 - 190 mg/dL和216 - 199 mg/dL,p = 0.0001)以及低密度脂蛋白胆固醇的血清水平(分别为128 - 112 mg/dL和140 - 127 mg/dL,p = 0.001)。口服疗法时甘油三酯的血清水平未显示出任何显著变化,而经皮疗法时这种脂质显著下降(128 - 101 mg/dL,p = 0.0001)。我们发现经皮疗法使高密度脂蛋白胆固醇显著降低,而口服疗法无显著变化。载脂蛋白AI是高密度脂蛋白2亚组分的主要蛋白质成分,口服疗法使其升高,经皮疗法使其降低。总之,我们发现两种疗法均降低了血清总胆固醇和低密度脂蛋白胆固醇,治疗之间无显著差异,而根据对血清甘油三酯和载脂蛋白AI的影响,治疗之间存在显著差异。

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