Collins Peter, Mosca Lori, Geiger Mary Jane, Grady Deborah, Kornitzer Marcel, Amewou-Atisso Messan G, Effron Mark B, Dowsett Sherie A, Barrett-Connor Elizabeth, Wenger Nanette K
Department of Cardiology, Royal Brompton and Harefield NHS Trust and NHLI, Imperial College London, Sydney Street, London, UK.
Circulation. 2009 Feb 24;119(7):922-30. doi: 10.1161/CIRCULATIONAHA.108.817577. Epub 2009 Feb 9.
The Raloxifene Use for The Heart (RUTH) trial showed that raloxifene, a selective estrogen receptor modulator, had no overall effect on the incidence of coronary events in women with established coronary heart disease or coronary heart disease risk factors. We provide detailed results of the effect of raloxifene on coronary outcomes over time and for 24 subgroups (17 predefined, 7 post hoc).
Postmenopausal women (n=10 101; mean age, 67 years) were randomized to raloxifene 60 mg/d or placebo for a median of 5.6 years. Coronary outcomes were assessed by treatment group in women with coronary heart disease risk factors and those with established coronary heart disease. Raloxifene had no effect on the incidence of coronary events in any subgroup except in the case of a post hoc age subgroup analysis using age categories defined in the Women's Health Initiative randomized trials. The effect of raloxifene on the incidence of coronary events differed significantly by age (interaction P=0.0118). The incidence of coronary events in women <60 years of age was significantly lower in those assigned raloxifene (50 events) compared with placebo (84 events; hazard ratio, 0.59; 95% confidence interval, 0.41 to 0.83; P=0.003; absolute risk reduction, 36 per 1000 women treated for 1 year). No difference was found between treatment groups in the incidence of coronary events in women > or =60 and <70 or > or =70 years of age.
In postmenopausal women at increased risk of coronary events, the overall lack of benefit of raloxifene was similar across the prespecified subgroups.
雷洛昔芬用于心脏疾病(RUTH)试验表明,选择性雌激素受体调节剂雷洛昔芬对已患有冠心病或有冠心病危险因素的女性的冠状动脉事件发生率无总体影响。我们提供了雷洛昔芬对冠状动脉结局随时间变化以及对24个亚组(17个预先定义的亚组,7个事后分析亚组)影响的详细结果。
绝经后女性(n = 10101;平均年龄67岁)被随机分为雷洛昔芬60 mg/d组或安慰剂组,中位治疗时间为5.6年。对有冠心病危险因素的女性和已患有冠心病的女性,按治疗组评估冠状动脉结局。雷洛昔芬对任何亚组的冠状动脉事件发生率均无影响,但在使用妇女健康倡议随机试验中定义的年龄类别进行事后年龄亚组分析时除外。雷洛昔芬对冠状动脉事件发生率的影响随年龄有显著差异(交互作用P = 0.0118)。年龄<60岁的女性中,分配到雷洛昔芬组的冠状动脉事件发生率(50例)显著低于安慰剂组(84例;风险比,0.59;95%置信区间,0.41至0.83;P = 0.003;每1000名接受1年治疗的女性的绝对风险降低36例)。在年龄≥60岁且<70岁或≥70岁的女性中,治疗组之间冠状动脉事件发生率未发现差异。
在冠状动脉事件风险增加的绝经后女性中,雷洛昔芬在预先指定的亚组中总体缺乏益处的情况相似。