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基线低密度脂蛋白胆固醇可改变冠状动脉疾病患者中脂蛋白(a)升高与全因死亡风险的关系。

Baseline Low-Density-Lipoprotein Cholesterol Modifies the Risk of All-Cause Death Associated With Elevated Lipoprotein(a) in Coronary Artery Disease Patients.

作者信息

Yao Younan, Liu Jin, Wang Bo, Zhou Ziyou, Lu Xiaozhao, Huang Zhidong, Deng Jingru, Yang Yongquan, Tan Ning, Chen Shiqun, Chen Jiyan, Liu Yong

机构信息

Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.

Guangdong Provincial Key Laboratory of Coronary Heart Disease Prevention, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.

出版信息

Front Cardiovasc Med. 2022 Jan 13;8:817442. doi: 10.3389/fcvm.2021.817442. eCollection 2021.

DOI:10.3389/fcvm.2021.817442
PMID:35097030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8792964/
Abstract

The prognostic value of elevated lipoprotein(a) [Lp(a)] in coronary artery disease (CAD) patients is inconsistent in previous studies, and whether such value changes at different low-density-lipoprotein cholesterol (LDL-C) levels is unclear. CAD patients treated with statin therapy from January 2007 to December 2018 in the Guangdong Provincial People's Hospital (NCT04407936) were consecutively enrolled. Individuals were categorized according to the baseline LDL-C at cut-off of 70 and 100 mg/dL. The primary outcome was 5-year all-cause death. Multivariate Cox proportional models and penalized spline analyses were used to evaluate the association between Lp(a) and all-cause mortality. Among 30,908 patients, the mean age was 63.1 ± 10.7 years, and 76.7% were men. A total of 2,383 (7.7%) patients died at 5-year follow-up. Compared with Lp(a) <50 mg/dL, Lp(a) ≥ 50 mg/dL predicted higher all-cause mortality (multivariable adjusted HR = 1.19, 95% CI 1.07-1.31) in the total cohort. However, when analyzed within each LDL-C category, there was no significant association between Lp(a) ≥ 50 mg/dL and higher all-cause mortality unless the baseline LDL-C was ≥ 100 mg/dL (HR = 1.19, 95% CI 1.04-1.36). The results from penalized spline analyses were robust. In statin-treated CAD patients, elevated Lp(a) was associated with increased risks of all-cause death, and such an association was modified by the baseline LDL-C levels. Patients with Lp(a) ≥ 50 mg/dL had higher long-term risks of all-cause death compared with those with Lp(a) <50 mg/dL only when their baseline LDL-C was ≥ 100 mg/dL.

摘要

脂蛋白(a)[Lp(a)]升高在冠状动脉疾病(CAD)患者中的预后价值在以往研究中并不一致,且这种价值在不同的低密度脂蛋白胆固醇(LDL-C)水平下是否会发生变化尚不清楚。连续纳入2007年1月至2018年12月在广东省人民医院接受他汀类药物治疗的CAD患者(NCT04407936)。根据基线LDL-C水平是否达到70和100mg/dL进行分类。主要结局为5年全因死亡。采用多变量Cox比例模型和惩罚样条分析来评估Lp(a)与全因死亡率之间的关联。在30908例患者中,平均年龄为63.1±10.7岁,男性占76.7%。共有2383例(7.7%)患者在5年随访期内死亡。在整个队列中,与Lp(a)<50mg/dL相比,Lp(a)≥50mg/dL预测全因死亡率更高(多变量校正HR=1.19,95%CI 1.07-1.31)。然而,在每个LDL-C类别中进行分析时,除非基线LDL-C≥100mg/dL,否则Lp(a)≥50mg/dL与更高的全因死亡率之间无显著关联(HR=1.19,95%CI 1.04-1.36)。惩罚样条分析结果稳健。在接受他汀类药物治疗的CAD患者中,Lp(a)升高与全因死亡风险增加相关,且这种关联受基线LDL-C水平的影响。仅当基线LDL-C≥100mg/dL时,Lp(a)≥50mg/dL的患者与Lp(a)<50mg/dL的患者相比,全因死亡的长期风险更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/8217b43bb44b/fcvm-08-817442-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/7cd39f266bd5/fcvm-08-817442-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/bf2ae8e53eea/fcvm-08-817442-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/30af803b7c27/fcvm-08-817442-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/e7753182fb1c/fcvm-08-817442-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/1428595ebdd4/fcvm-08-817442-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/8217b43bb44b/fcvm-08-817442-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/7cd39f266bd5/fcvm-08-817442-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/bf2ae8e53eea/fcvm-08-817442-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/30af803b7c27/fcvm-08-817442-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/e7753182fb1c/fcvm-08-817442-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/1428595ebdd4/fcvm-08-817442-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd3b/8792964/8217b43bb44b/fcvm-08-817442-g0006.jpg

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