Ridker P M, Hennekens C H, Stampfer M J
Department of Medicine, Brigham and Women's Hospital, Boston, MA 02215-1204.
JAMA. 1993 Nov 10;270(18):2195-9.
To assess prospectively the risk of myocardial infarction (MI) associated with elevated levels of lipoprotein(a) (Lp[a]).
Nested case-control study using prospectively collected plasma samples.
Participants in the Physicians' Health Study.
A total of 14,916 male physicians aged 40 to 84 years with no prior history of MI or stroke provided plasma samples at baseline and were followed up prospectively for an average period of 60.2 months. Samples from 296 physicians who subsequently developed MI were analyzed for Lp(a) level together with paired controls, matched for smoking status and age.
Fatal or nonfatal acute MI.
The distribution of Lp(a) level among cases was virtually identical to that of controls (P = .88), and there was no significant difference between groups for median Lp(a) levels (103.0 mg/L vs 102.5 mg/L; P = .73). In analyses controlling for age and smoking status, we found no evidence of association between increasing level of Lp(a) and risk of MI (relative risks from lowest to highest quintiles of Lp(a): 1.00, 0.97, 0.83, 0.88, and 1.07; P for trend = .93) or a threshold effect at any prespecified cutoff of Lp(a) level (relative risks associated with Lp[a] levels above the 25th, 50th, 75th, 90th, and 95th percentiles of the control distribution, respectively: 1.04, 1.00, 1.19, 1.00, and 1.07; all P values nonsignificant). Further adjustment for both lipid and nonlipid cardiovascular risk factors had no material impact.
In this prospective study of predominantly middle-aged white men, we found no evidence of association between Lp(a) level and risk of future MI. These data do not support the use of Lp(a) level as a screening tool to define cardiovascular risk among this population.
前瞻性评估脂蛋白(a)[Lp(a)]水平升高与心肌梗死(MI)风险之间的关系。
利用前瞻性收集的血浆样本进行巢式病例对照研究。
医师健康研究的参与者。
共有14916名年龄在40至84岁之间、既往无心肌梗死或中风病史的男性医师在基线时提供了血浆样本,并进行了平均60.2个月的前瞻性随访。对296名随后发生心肌梗死的医师的样本以及配对的对照样本进行Lp(a)水平分析,对照样本根据吸烟状况和年龄进行匹配。
致命性或非致命性急性心肌梗死。
病例组中Lp(a)水平的分布与对照组几乎相同(P = 0.88),两组的Lp(a)中位数水平无显著差异(103.0 mg/L对102.5 mg/L;P = 0.73)。在控制年龄和吸烟状况的分析中,我们没有发现Lp(a)水平升高与心肌梗死风险之间存在关联的证据(Lp(a)从最低到最高五分位数的相对风险分别为:1.00、0.97、0.83、0.88和1.07;趋势P值 = 0.93),也没有发现Lp(a)水平在任何预先设定的临界值处存在阈值效应(与高于对照组分布第25、50、75、90和95百分位数的Lp(a)水平相关的相对风险分别为:1.04、1.00、1.19、1.00和1.07;所有P值均无统计学意义)。进一步调整脂质和非脂质心血管危险因素对结果没有实质性影响。
在这项主要针对中年白人男性的前瞻性研究中,我们没有发现Lp(a)水平与未来心肌梗死风险之间存在关联的证据。这些数据不支持将Lp(a)水平用作该人群心血管风险的筛查工具。