Robinson Jennifer G, Wallace Robert, Limacher Marian, Ren Hong, Cochrane Barbara, Wassertheil-Smoller Sylvia, Ockene Judith K, Blanchette Patricia L, Ko Marcia G
Department of Epidemiology, University of Iowa, Iowa City, Iowa, USA.
Am J Cardiol. 2008 Sep 15;102(6):693-9. doi: 10.1016/j.amjcard.2007.12.044. Epub 2008 Jul 2.
Women discharged with diagnoses of nonspecific chest pain (NSCP) may be at increased risk for subsequent coronary artery disease (CAD) events. The influence of hormone therapy on NSCP is unknown. The Women's Health Initiative (WHI) enrolled postmenopausal women aged 50 to 79 years. The duration of follow-up was 7.1 years in the WHI Estrogen-Alone trial (E-Alone) and 5.6 years in the WHI Estrogen Plus Progestin trial (E+P). After excluding women with previous cardiovascular disease, 9,427 women in E-Alone and 15,105 women in E+P were included in this analysis. NSCP, defined as having a primary hospital discharge diagnosis of NSCP by International Classification of Diseases, Ninth Revision, code, was reported in 322 women in E-Alone and 249 in E+P. Risks for subsequent CAD events were estimated using intent-to-treat Cox proportional-hazards models stratified by clinic and adjusted for age and other risk factors. In the fully adjusted models of the combined trials, women with NSCP had a twofold greater risk for subsequent nonfatal CAD events, including nonfatal myocardial infarction (2.3% vs 1.7%, hazard ratio [HR] 2.10, 95% confidence interval [CI] 1.11 to 3.98), revascularization (3.5% vs 2.6%, HR 1.99, 95% CI 1.20 to 3.30), and hospitalized angina (3.7% vs 2.3%, HR 2.39, 95% CI 1.46 to 3.92). Hormone therapy did not appear to have a significant effect on either the incidence of NSCP hospitalizations (E-Alone: HR 1.04, 95% CI 0.81 to 1.32; E+P: HR 0.78, 95% CI 0.59 to 1.02) or the risk for a subsequent CAD event. In conclusion, a hospitalization for NSCP doubles the risk for a subsequent CAD event in postmenopausal women over the next 5 to 7 years and identifies them as candidates for aggressive risk factor treatment.
被诊断为非特异性胸痛(NSCP)出院的女性,后续发生冠状动脉疾病(CAD)事件的风险可能会增加。激素疗法对NSCP的影响尚不清楚。妇女健康倡议(WHI)纳入了年龄在50至79岁的绝经后女性。在WHI单纯雌激素试验(E-单独)中的随访时间为7.1年,在WHI雌激素加孕激素试验(E+P)中的随访时间为5.6年。在排除既往有心血管疾病的女性后,本分析纳入了E-单独试验中的9427名女性和E+P试验中的15105名女性。NSCP定义为根据国际疾病分类第九版编码在医院出院时主要诊断为NSCP,E-单独试验中有322名女性报告了该情况,E+P试验中有249名女性报告了该情况。使用意向性治疗Cox比例风险模型,按诊所分层并对年龄和其他风险因素进行调整,估计后续CAD事件的风险。在联合试验的完全调整模型中,患有NSCP的女性发生后续非致命CAD事件的风险增加两倍,包括非致命性心肌梗死(2.3%对1.7%,风险比[HR]2.10,95%置信区间[CI]1.11至3.98)、血运重建(3.5%对2.6%,HR 1.99,95%CI 1.20至3.30)和住院心绞痛(3.7%对2.3%,HR 2.39,95%CI 1.46至3.92)。激素疗法似乎对NSCP住院发生率(E-单独:HR 1.04,95%CI 0.81至1.32;E+P:HR 0.78,95%CI 0.59至1.02)或后续CAD事件风险均无显著影响。总之,因NSCP住院使绝经后女性在接下来5至7年发生后续CAD事件的风险加倍,并将她们确定为积极进行风险因素治疗的对象。