首页> 外文期刊>JAMA: the Journal of the American Medical Association >Effect of estrogen plus progestin on stroke in postmenopausal women: the Women's Health Initiative: a randomized trial.
【24h】

Effect of estrogen plus progestin on stroke in postmenopausal women: the Women's Health Initiative: a randomized trial.

机译:雌激素和孕激素对绝经后妇女中风的影响:《妇女健康倡议》:一项随机试验。

获取原文
获取原文并翻译 | 示例
       

摘要

CONTEXT: The Women's Health Initiative (WHI) trial of estrogen plus progestin was stopped early because of adverse effects, including an increased risk of stroke in the estrogen plus progestin group. OBJECTIVE: To assess the effect of estrogen plus progestin on ischemic and hemorrhagic stroke and in subgroups, and to determine whether the effect of estrogen plus progestin was modified by baseline levels of blood biomarkers. DESIGN: Multicenter double-blind, placebo-controlled, randomized clinical trial involving 16 608 women aged 50 through 79 years with an average follow-up of 5.6 years. Baseline levels of blood-based markers of inflammation, thrombosis, and lipid levels were measured in the first 140 centrally confirmed stroke cases and 513 controls. INTERVENTIONS: Participants received 0.625 mg/d of conjugated equine estrogen plus 2.5 mg/d of medroxyprogesterone acetate (n = 8506) or placebo (n = 8102). MAIN OUTCOME MEASURES: Overall strokes and stroke subtype and severity were centrally adjudicatedby stroke neurologists. RESULTS: One hundred fifty-one patients (1.8%) in the estrogen plus progestin and 107 (1.3%) in the placebo groups had strokes. Overall 79.8% of strokes were ischemic. For combined ischemic and hemorrhagic strokes, the intention-to-treat hazard ratio (HR) for estrogen plus progestin vs placebo was 1.31 (95% confidence interval [CI], 1.02-1.68); with adjustment for adherence, the HR was 1.50 (95% CI, 1.08-2.08). The HR for ischemic stroke was 1.44 (95% CI, 1.09-1.90) and for hemorrhagic stroke, 0.82 (95% CI, 0.43-1.56). Point estimates of the HRs indicate that excess risk of all stroke was apparent in all age groups, in all categories of baseline stroke risk, and in women with and without hypertension, prior history of cardiovascular disease, use of hormones, statins, or aspirin. Other risk factors for stroke, including smoking, blood pressure, diabetes, lower use of vitamin C supplements, blood-based biomarkers of inflammation, higher white blood cell count, and higher hematocrit levels did not modify the effect of estrogen plus progestin on stroke risk. CONCLUSIONS: Estrogen plus progestin increases the risk of ischemic stroke in generally healthy postmenopausal women. Excess risk for all strokes attributed to estrogen plus progestin appeared to be present in all subgroups of women examined.
机译:背景:由于不利影响,包括雌激素加孕激素组中风的风险增加,妇女健康倡议(WHI)的雌激素加孕激素试验被提前终止。目的:评估雌激素加孕激素对缺血性和出血性中风及亚组的影响,并确定是否通过血液生物标志物的基线水平改变雌激素加孕激素的作用。设计:多中心双盲,安慰剂对照,随机临床试验,纳入16608名年龄在50至79岁之间的女性,平均随访5.6年。在前140例经中央确认的卒中病例和513例对照中,测量了基于血液的炎症,血栓形成和脂质指标的基线水平。干预措施:参与者接受0.625 mg / d的共轭马雌激素加2.5 mg / d的醋酸甲羟孕酮(n = 8506)或安慰剂(n = 8102)。主要观察指标:中风神经病学专家对总体卒中,卒中亚型和严重程度进行了总体评估。结果:雌激素加孕激素的151名患者(1.8%)和安慰剂组的107名患者(1.3%)患有中风。总体有79.8%的中风是缺血性的。对于合并缺血性和出血性中风,雌激素加孕激素与安慰剂的意向治疗危险比(HR)为1.31(95%置信区间[CI],1.02-1.68);调整依从性后,HR为1.50(95%CI,1.08-2.08)。缺血性中风的HR为1.44(95%CI,1.09-1.90),出血性中风的HR为0.82(95%CI,0.43-1.56)。 HR的点估计值表明,在所有年龄段,所有类别的中风风险中,以及患有和不患有高血压的女性,心血管疾病的既往史,使用激素,他汀类或阿司匹林的妇女中,所有中风的过度风险都明显。其他中风的危险因素,包括吸烟,血压,糖尿病,维生素C补充剂的使用减少,血液中炎症的生物标志物,白细胞计数较高和血细胞比容水平较高,并未改变雌激素和孕激素对中风风险的影响。 。结论:雌激素加孕激素会增加一般健康的绝经后妇女发生缺血性中风的风险。在所有接受检查的女性亚组中,均归因于雌激素和孕激素的所有中风的风险均较高。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号