Denes Pablo, Larson Joseph C, Lloyd-Jones Donald M, Prineas Ronald J, Greenland Philip
Department of Medicine, Northwestern University, Feinberg School of Medicine, Chicago, Ill 60611, USA.
JAMA. 2007 Mar 7;297(9):978-85. doi: 10.1001/jama.297.9.978.
Data are sparse regarding the prevalence, incidence, and independent prognostic value of minor and/or major electrocardiographic (ECG) abnormalities in asymptomatic postmenopausal women. There is no information on the effect, if any, of hormonal treatment on the prognostic value of the ECG.
To examine association of minor and major baseline and incident ECG abnormalities with long-term cardiovascular morbidity and mortality.
DESIGN, SETTING, AND PARTICIPANTS: Post-hoc analysis of the estrogen plus progestin component of the Women's Health Initiative study, a randomized controlled primary prevention trial of 14 749 postmenopausal asymptomatic women with intact uterus who received 1 daily tablet containing 0.625 mg of oral conjugated equine estrogen and 2.5 mg of medroxyprogesterone acetate or a matching placebo. Participants were enrolled from 1993 to 1998, and the estrogen plus progestin trial was stopped on July 7, 2002.
The Novacode criteria were used to define minor, major, and incident ECG abnormalities. Cardiovascular end points included incident coronary heart disease (CHD) and cardiovascular disease (CVD) events.
Among women with absent (n = 9744), minor (n = 4095), and major (n = 910) ECG abnormalities, there were 118, 91, and 37 incident CHD events, respectively. The incident annual CHD event rates per 10 000 women with absent, minor, or major ECG abnormalities were 21 (95% confidence interval [CI], 18-26), 40 (95% CI, 32-49), and 75 (95% CI, 54-104), respectively. After 3 years of follow-up, 5% of women who had normal ECG at baseline developed new ECG abnormalities with an annual CHD event rate of 85 (95% CI, 44-164) per 10 000 women. The adjusted hazard ratios for CHD events were 1.55 (95% CI, 1.14-2.11) for minor baseline, 3.01 (95% CI, 2.03-4.46) for major baseline, and 2.60 (95% CI, 1.08-6.27) for incident ECG abnormalities. There were no significant interactions between hormone treatment assignment and ECG abnormalities for risk prediction of cardiovascular end points. For prediction of CHD events, the addition of ECG findings to the Framingham risk score increased from 0.69 to 0.74 the area under the receiver operating characteristic curve. Similar findings were found for incident CVD events.
Among asymptomatic postmenopausal women, clinically relevant baseline and incident ECG abnormalities are independently associated with increased risk of cardiovascular events and mortality, and the information is incremental to the established method of risk stratification.
clinicaltrials.gov Identifier: NCT00000611.
关于无症状绝经后女性轻微和/或严重心电图(ECG)异常的患病率、发病率及独立预后价值的数据稀少。关于激素治疗对心电图预后价值的影响(若有)尚无相关信息。
研究轻微和严重基线及新发心电图异常与长期心血管疾病发病率和死亡率之间的关联。
设计、地点和参与者:对妇女健康倡议研究中雌激素加孕激素部分进行事后分析,这是一项随机对照的一级预防试验,纳入了14749名子宫完整的无症状绝经后女性,她们每日服用一片含有0.625mg口服结合马雌激素和2.5mg醋酸甲羟孕酮的片剂或匹配的安慰剂。参与者于1993年至1998年入组,雌激素加孕激素试验于2002年7月7日停止。
采用诺瓦科德标准定义轻微、严重和新发心电图异常。心血管终点包括新发冠心病(CHD)和心血管疾病(CVD)事件。
在心电图正常(n = 9744)、轻微异常(n = 4095)和严重异常(n = 910)的女性中,分别有118例、91例和37例新发冠心病事件。每10000名心电图正常、轻微异常或严重异常的女性中,每年新发冠心病事件发生率分别为21(95%置信区间[CI],18 - 26)、40(95% CI,32 - 49)和75(95% CI,54 - 104)。经过3年随访,基线心电图正常的女性中有5%出现了新的心电图异常,每10000名女性中每年新发冠心病事件发生率为85(95% CI,44 - 164)。调整后的冠心病事件风险比,轻微基线异常为1.55(95% CI,1.14 - 2.11),严重基线异常为3.01(95% CI,2.03 - 4.46),新发心电图异常为2.60(95% CI,1.08 - 6.27)。在心血管终点风险预测方面,激素治疗分组与心电图异常之间无显著交互作用。对于冠心病事件预测,将心电图结果添加到弗雷明汉风险评分中,受试者操作特征曲线下面积从0.69增加到0.74。新发CVD事件也有类似发现。
在无症状绝经后女性中,临床相关的基线和新发心电图异常与心血管事件和死亡风险增加独立相关,且该信息对既定的风险分层方法具有增量价值。
clinicaltrials.gov标识符:NCT00000611。