Walker I D, Davidson J F, Richards A, Yates R, McEwan H P
Thromb Haemost. 1985 Jun 24;53(3):303-5.
Two groups of postmenopausal women were compared. One group of 13 was given the synthetic steroid Org OD14 to suppress climacteric symptoms and one group of 14 was given placebo. After a 2 week baseline period the subjects received daily for 12 weeks, either 2.5 mg Org OD14 or placebo. There were no significant differences between the groups pre-treatment. Compared with the placebo group, during treatment, the Org OD14 group showed the following significant differences: higher haemoglobin, haematocrit, platelet count, plasminogen, fibrinolytic activity on fibrin plates and antithrombin III and lower fibrinogen. No significant differences between the groups were found in alpha 2 antiplasmin levels, total cholesterol, total triglycerides, bilirubin or transaminase levels but the Org OD14 group had significantly lower levels of HDL cholesterol. With the exception of the haemoglobin and haematocrit levels all of the differences had disappeared by 2 weeks post treatment.
对两组绝经后女性进行了比较。一组13名女性服用合成类固醇Org OD14以抑制更年期症状,另一组14名女性服用安慰剂。在为期2周的基线期后,受试者连续12周每日服用2.5毫克Org OD14或安慰剂。治疗前两组之间无显著差异。与安慰剂组相比,治疗期间,Org OD14组出现了以下显著差异:血红蛋白、血细胞比容、血小板计数、纤溶酶原、纤维蛋白平板上的纤溶活性和抗凝血酶III更高,纤维蛋白原更低。两组在α2抗纤溶酶水平、总胆固醇、总甘油三酯、胆红素或转氨酶水平上未发现显著差异,但Org OD14组的高密度脂蛋白胆固醇水平显著更低。除血红蛋白和血细胞比容水平外,所有差异在治疗后2周时均已消失。