Prognostic impact of lipoprotein(a) in patients undergoing percutaneous coronary intervention modified by low density lipoprotein cholesterol

被引:2
作者
Xu, Na [1 ]
Yuan, Deshan [1 ]
Yao, Yi [1 ]
Jiang, Lin [1 ]
Xu, Jingjing [1 ]
Tang, Xiaofang [1 ]
Song, Ying [1 ]
Gao, Lijian [1 ]
Chen, Jue [1 ]
Song, Lei [1 ]
Zhao, Xueyan [1 ]
Chen, Jilin [1 ]
Yang, Yuejin [1 ]
Xu, Bo [1 ]
Gao, Runlin [1 ,2 ]
Yuan, Jinqing [1 ,2 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Cardiovasc Dis, State Key Lab Cardiovasc Dis, Fu Wai Hosp,Natl Ctr Cardiovasc Dis, Beijing, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Dept Cardiol, Natl Clin Res Ctr Cardiovasc Dis, State Key Lab Cardiovasc Dis,Fu Wai Hosp,Natl Ctr, 167 Beilishi Rd, Beijing 100037, Peoples R China
关键词
Lipoprotein(a); Low density lipoprotein cholesterol; Long -term survival; ASSOCIATION; EVENTS; RISK; DISEASE;
D O I
10.1016/j.cca.2023.117217
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: It is well established that lipoprotein(a)[Lp(a)] and low-density lipoprotein cholesterol (LDL-C) play a vital role in atherosclerosis. We investigated the prevalence and prognostic implications of increased Lp(a) in patients undergoing percutaneous coronary intervention (PCI) according to different LDL-C concentrations.Methods: A total of 9,190 patients with CAD after PCI were consecutively enrolled in the study and subsequently divided into three groups according to baseline LDL-C at cut-off of 70 and 100 mg/dl. Increased Lp(a) was defined as > 30 mg/dl. The primary endpoint was all-cause death. Second endpoint was cardiac death. Cox regression, Kaplan-Meier and Sensitivity analysis were performed.Results: During an average of 5.0 y of follow-up, 354 (3.9 %) patients experienced all-cause death with 213(2.3 %) of whom from cardiac death. Increased Lp(a) was present in 25.7 %, 34.2 %, and 40.6 % across the LDL-C < 70, 70-100 and >= 100 mg/dl groups, respectively. After multivariate adjustment, Lp(a) elevation remained significantly associated with 5-y all-cause death (adjusted HR, 1.243; 95 % CI 1.001-1.544; p = 0.048) in the total cohort and only in those with LDL-C >= 100 mg/dl (adjusted HR, 1.642; 95 % CI 1.139-2.367; p = 0.008) when analyzed within each LDL-C category. Consistently with the results of associations between Lp(a) and cardiac death (adjusted HR, 1.534; 95 % CI 1.164-2.021; p = 0.002 for total cohort and adjusted HR, 2.404; 95 % CI 1.439-3.872; p < 0.001 for LDL-C >= 100 mg/dl). And this relationship holds after adjusting for LDL-Ccorr additionally. These findings are confirmed again in sensitivity analyses that excluded patients with Lp(a) con-centrations in the top or the bottom 5 %.Conclusions: We confirmed that increased Lp(a) was associated with increased risk of long-term outcomes, and such an association was modified by the baseline LDL-C concentrations. Screening of high Lp(a) in individuals with elevations of LDL-C may enables risk stratification for poor prognosis.
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页数:8
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