Dias A R, Melo R N, Gebara O C E, D'Amico E A, Nussbacher A, Halbe H W, Pinotti J A
Gynecology and Obstetrics Department School of Medicine, University of São Paulo, Brazil.
Climacteric. 2005 Mar;8(1):63-70. doi: 10.1080/13697130500042581.
To compare the effect of conjugated equine estrogens (CEE) and raloxifene on lipid profile and hemostasis.
A double-blind, randomized and parallel study was performed with 90 healthy postmenopausal women, aged 54 +/- 5 years, divided into three groups and submitted to daily therapy with either CEE 0.625 mg, raloxifene 60 mg or placebo for 4 months. The lipid profile, coagulation and fibrinolytic factors were analyzed.
CEE increased the levels of high density lipoprotein cholesterol (HDL-C) from 49.0 to 56.8 mg/dl (p < 0.001), very low density lipoprotein cholesterol (VLDL-C) from 17.2 to 22.3 mg/dl (p < 0.001), and triglycerides from 86.0 to 111.7 mg/dl (p < 0.001), and decreased the levels of low density lipoprotein cholesterol (LDL-C) from 121.0 to 106.5 mg/dl (p < 0.001). The only significant effect of raloxifene was an increase in the levels of HDL-C from 46.0 to 47.8 mg/dl (p = 0.019). There was no significant reduction in LDL-C, from 115.5 to 110.2 mg/dl (p = 0.06), VLDL-C, from 21.7 to 20.0 mg/dl (p = 0.201), and triglycerides, from 108 to 100 mg/dl (p = 0.201). CEE decreased the levels of fibrinogen, from 370.5 to 326.8 g/l (p = 0.039) and the levels of antithrombin III, from 99.5 to 93.2% (p < 0.001). Raloxifene decreased the levels of fibrinogen, from 354.7 to 302.0 g/l (p = 0.009) and the levels of antithrombin III, from 102.4 to 98.5% (p = 0.039). CEE increased levels of protein C from 103.7 to 115.3 mg/l (p < 0.001) and raloxifene did not change the levels of protein C (107.9 to 105.1 mg/l; p = 0.158). CEE decreased the antigen levels of tissue plasminogen activator (t-PA) from 8.8 to 6.8 U/ml (p < 0.001), and of plasminogen activator inhibitor (PAI-1) from 30.8 to 21.6 U/ml (p < 0.010), whereas raloxifene had no significant effect on either t-PA, from 9.6 to 9.2 U/ml (p = 0.235) or PAI-1 antigen levels, from 32.1 to 30.4 U/ml (p = 0.538). CONCLUSION Both CEE and raloxifene exert significant effects on the lipid and coagulation profile. CEE had a more significant effect on fibrinolysis than raloxifene. These effects may have a significant impact on the cardiovascular risk that needs to be confirmed in larger studies.
比较结合马雌激素(CEE)和雷洛昔芬对血脂谱和止血的影响。
对90名年龄在54±5岁的健康绝经后女性进行了一项双盲、随机平行研究,将其分为三组,分别接受每日0.625mg CEE、60mg雷洛昔芬或安慰剂治疗4个月。分析血脂谱、凝血和纤溶因子。
CEE使高密度脂蛋白胆固醇(HDL-C)水平从49.0mg/dl升至56.8mg/dl(p<0.001),极低密度脂蛋白胆固醇(VLDL-C)从17.2mg/dl升至22.3mg/dl(p<0.001),甘油三酯从86.0mg/dl升至111.7mg/dl(p<0.001),低密度脂蛋白胆固醇(LDL-C)水平从121.0mg/dl降至106.5mg/dl(p<0.001)。雷洛昔芬的唯一显著作用是使HDL-C水平从46.0mg/dl升至47.8mg/dl(p=0.019)。LDL-C从115.5mg/dl降至110.2mg/dl(p=0.06)、VLDL-C从21.7mg/dl降至20.0mg/dl(p=0.201)、甘油三酯从108mg/dl降至100mg/dl(p=0.201)均无显著降低。CEE使纤维蛋白原水平从370.5g/l降至326.8g/l(p=0.039),抗凝血酶III水平从99.5%降至93.2%(p<0.001)。雷洛昔芬使纤维蛋白原水平从354.7g/l降至302.0g/l(p=0.009)以及抗凝血酶III水平从102.4%降至98.5%(p=0.039)。CEE使蛋白C水平从103.7mg/l升至115.3mg/l(p<0.001),而雷洛昔芬未改变蛋白C水平(从107.9mg/l至105.1mg/l;p=0.158)。CEE使组织型纤溶酶原激活剂(t-PA)抗原水平从8.8U/ml降至6.8U/ml(p<0.001),纤溶酶原激活剂抑制剂(PAI-1)从30.8U/ml降至21.6U/ml(p<0.010),而雷洛昔芬对t-PA(从9.6U/ml至9.2U/ml;p=0.235)或PAI-1抗原水平(从32.1U/ml至30.4U/ml;p=0.538)均无显著影响。结论CEE和雷洛昔芬对血脂和凝血谱均有显著影响。CEE对纤溶的影响比雷洛昔芬更显著。这些影响可能对心血管风险有显著影响,需要在更大规模研究中得到证实。