Waters David D, Alderman Edwin L, Hsia Judith, Howard Barbara V, Cobb Frederick R, Rogers William J, Ouyang Pamela, Thompson Paul, Tardif Jean Claude, Higginson Lyall, Bittner Vera, Steffes Michael, Gordon David J, Proschan Michael, Younes Naji, Verter Joel I
Division of Cardiology, Room 5G1, San Francisco General Hospital, 1001 Potrero Ave, San Francisco, CA 94110, USA.
JAMA. 2002 Nov 20;288(19):2432-40. doi: 10.1001/jama.288.19.2432.
Hormone replacement therapy (HRT) and antioxidant vitamins are widely used for secondary prevention in postmenopausal women with coronary disease, but no clinical trials have demonstrated benefit to support their use.
To determine whether HRT or antioxidant vitamin supplements, alone or in combination, influence the progression of coronary artery disease in postmenopausal women, as measured by serial quantitative coronary angiography.
DESIGN, SETTING, AND PATIENTS: The Women's Angiographic Vitamin and Estrogen (WAVE) Trial, a randomized, double-blind trial of 423 postmenopausal women with at least one 15% to 75% coronary stenosis at baseline coronary angiography. The trial was conducted from July 1997 to January 2002 in 7 clinical centers in the United States and Canada.
Patients were randomly assigned in a 2 x 2 factorial design to receive either 0.625 mg/d of conjugated equine estrogen (plus 2.5 mg/d of medroxyprogesterone acetate for women who had not had a hysterectomy), or matching placebo, and 400 IU of vitamin E twice daily plus 500 mg of vitamin C twice daily, or placebo.
Annualized mean (SD) change in minimum lumen diameter (MLD) from baseline to concluding angiogram of all qualifying coronary lesions averaged for each patient. Patients with intercurrent death or myocardial infarction (MI) were imputed the worst rank of angiographic outcome.
The mean (SD) interval between angiograms was 2.8 (0.9) years. Coronary progression, measured in mean (SD) change, worsened with HRT by 0.047 (0.15) mm/y and by 0.024 (0.15) mm/y with HRT placebo (P =.17); and for antioxidant vitamins by 0.044 (0.15) mm/y and with vitamin placebo by 0.028 (0.15) mm/y (P =.32). When patients with intercurrent death or MI were included, the primary outcome showed an increased risk for women in the active HRT group (P =.045), and suggested an increased risk in the active vitamin group (P =.09). Fourteen patients died in the HRT group and 8 in the HRT placebo group (hazard ratio [HR], 1.8; 95% confidence interval [CI], 0.75-4.3), and 16 in the vitamin group and 6 in the vitamin placebo group (HR, 2.8; 95% CI, 1.1-7.2). Death, nonfatal MI, or stroke occurred in 26 HRT patients vs 15 HRT controls (HR, 1.9; 95% CI, 0.97-3.6) and in 26 vitamin patients and 18 vitamin controls (HR, 1.5; 95% CI, 0.80-2.9). There was no interaction between the 2 treatment interventions.
In postmenopausal women with coronary disease, neither HRT nor antioxidant vitamin supplements provide cardiovascular benefit. Instead, a potential for harm was suggested with each treatment.
激素替代疗法(HRT)和抗氧化维生素被广泛用于绝经后冠心病女性的二级预防,但尚无临床试验证明其使用有益。
通过连续定量冠状动脉造影,确定HRT或抗氧化维生素补充剂单独或联合使用是否会影响绝经后女性冠状动脉疾病的进展。
设计、地点和患者:女性血管造影维生素和雌激素(WAVE)试验,一项对423名绝经后女性进行的随机双盲试验,这些女性在基线冠状动脉造影时至少有一处15%至75%的冠状动脉狭窄。该试验于1997年7月至2002年1月在美国和加拿大的7个临床中心进行。
患者按2×2析因设计随机分组,分别接受0.625mg/d结合马雌激素(未行子宫切除术的女性加用2.5mg/d醋酸甲羟孕酮)或匹配的安慰剂,以及每日两次400IU维生素E加每日两次500mg维生素C或安慰剂。
每位患者所有符合条件的冠状动脉病变从基线到末次血管造影的最小管腔直径(MLD)的年化平均(标准差)变化。并发死亡或心肌梗死(MI)的患者被赋予血管造影结局的最差等级。
血管造影之间的平均(标准差)间隔为2.8(0.9)年。以平均(标准差)变化衡量的冠状动脉进展,HRT组恶化0.047(0.15)mm/年,HRT安慰剂组恶化0.024(0.15)mm/年(P=0.17);抗氧化维生素组恶化0.044(0.15)mm/年,维生素安慰剂组恶化0.028(0.15)mm/年(P=0.32)。纳入并发死亡或MI的患者后,主要结局显示活性HRT组女性风险增加(P=0.045),活性维生素组有风险增加迹象(P=0.09)。HRT组14例患者死亡,HRT安慰剂组8例(风险比[HR],1.8;95%置信区间[CI],0.75-4.3),维生素组16例患者死亡,维生素安慰剂组6例(HR,2.8;95%CI=1.1-7.2)。26例HRT患者发生死亡、非致命MI或卒中,HRT对照组15例(HR,1.9;95%CI,0.97-3.6);26例维生素组患者发生上述情况,维生素对照组18例(HR,1.5;95%CI,0.80-2.9)。两种治疗干预之间无相互作用。
在绝经后冠心病女性中,HRT和抗氧化维生素补充剂均未提供心血管益处。相反,每种治疗都提示有潜在危害。