Joint Association of Lipoprotein(a) and a Family History of Coronary Artery Disease with the Cardiovascular Outcomes in Patients with Chronic Coronary Syndrome

被引:0
作者
Liu, Hui -Hui [1 ,2 ]
Li, Sha [1 ]
Zhang, Yan [1 ]
Guo, Yuan-Lin [1 ]
Zhu, Cheng-Gang [1 ]
Wu, Na-Qiong [1 ]
Gao, Ying [1 ]
Xu, Rui-Xia [1 ]
Dong, Qian [1 ]
Li, Jian-Jun [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Cardiometab Ctr, Natl Ctr Cardiovasc Dis,State Key Lab Cardiovasc D, 167 BeiLiShi Rd, Beijing 100037, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Fuwai Hosp, Heart Failure Ctr, Natl Ctr Cardiovasc Dis,State Key Lab Cardiovasc D, Beijing, Peoples R China
关键词
Lipoprotein(a); Family history; Cardiovascular event; Chronic coronary syndrome; Risk factor; CLINICAL-OUTCOMES; FUTURE CORONARY; RISK; MANAGEMENT; IMPACT; DYSLIPIDEMIA; GUIDELINES; EVENTS; STATIN;
D O I
10.5551/jat.64693
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Aim: No data are currently available regarding the association between Lp(a) and the cardiovascular outcomes in patients with coronary artery disease (CAD) according to their family history (FHx) of CAD. This study aimed to evaluate the significance of Lp(a) in predicting major adverse cardiovascular events (MACEs) in patients with chronic coronary syndrome (CCS) with or without FHx. Methods: A total of 6056 patients with CCS were enrolled. Information on FHx was collected, and the plasma Lp(a) levels were measured. All patients were followed up regularly. The independent and joint associations of Lp(a) and FHx with the risk of MACEs, including cardiovascular death, nonfatal myocardial infarction, and stroke, were analyzed. Results: With over an average of 50.35 +/- 18.58 months follow-up, 378 MACEs were recorded. A Cox regression analysis showed an elevated Lp(a) level to be an independent predictor for MACEs in patients with [hazard ratio (HR): 2.77, 95% confidence interval (CI): 1.38-5.54] or without FHx (HR: 1.35, 95% CI: 1.02-1.77). In comparison to subjects with non-elevated Lp(a) and negative FHx, patients with elevated Lp(a) alone were at a nominally higher risk of MACEs (HR: 1.26, 95% CI: 0.96-1.67), while those with both had the highest risk (HR: 1.93, 95% CI: 1.14-3.28). Moreover, adding Lp(a) to the original model increased the C-statistic by 0.048 in subjects with FHx (p=0.004) and by 0.004 in those without FHx (p=0.391). Conclusions: The present study is the first to suggest that Lp(a) could be used to predict MACEs in CCS patients with or without FHx; however, its prognostic significance was more noteworthy in patients with FHx.
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页码:1319 / 1332
页数:14
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