Lipoprotein(a), Oxidized Phospholipids, and Coronary Artery Disease Severity and Outcomes

被引:46
|
作者
Gilliland, Thomas C. [1 ,2 ,3 ]
Liu, Yuxi [1 ]
Mohebi, Reza [1 ]
Miksenas, Hannah [1 ]
Haidermota, Sara [1 ,2 ]
Wong, Megan [1 ,2 ]
Hu, Xingdi [4 ]
Cristino, Joaquim Rosado [4 ]
Browne, Auris [4 ]
Plutzky, Jorge [3 ,5 ]
Tsimikas, Sotirios [6 ]
Januzzi Jr, James L. [1 ,3 ,7 ]
Natarajan, Pradeep [1 ,2 ,8 ]
机构
[1] Massachusetts Gen Hosp, Div Cardiol, Boston, MA USA
[2] Broad Inst Harvard, Program Med & Pop ulat Genet & Cardiovasc Dis Init, Cambridge, MA USA
[3] Harvard Med Sch, Dept Med, Boston, MA USA
[4] Novartis Pharmaceut, E Hanover, NJ USA
[5] Brigham & Womens Hosp, Div Cardiol, Boston, MA USA
[6] Univ Calif San Diego, Sulpizio Cardiovasc Ctr, La Jolla, CA USA
[7] Baim Inst Clin Res, Boston, MA USA
[8] Massachusetts Gen Hosp, 185 Cambridge St,CPZN 3-184, Boston, MA 02114 USA
关键词
atherosclerosis; coronary artery disease; lipids and lipoproteins; lipoprotein(a); CARDIOVASCULAR RISK-FACTORS; LOW-DENSITY-LIPOPROTEIN; ELEVATED LIPOPROTEIN(A); APOLIPOPROTEIN B-100; LP(A) LIPOPROTEIN; ASSOCIATION; THERAPY; ATHEROSCLEROSIS; ALIROCUMAB;
D O I
10.1016/j.jacc.2023.02.050
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Lipoprotein(a) (Lp[a]) and oxidized phospholipids (OxPLs) are each independent risk factors for atherosclerotic cardiovascular disease. The extent to which Lp(a) and OxPLs predict coronary artery disease (CAD) severity and outcomes in a contemporary, statin-treated cohort is not well established. OBJECTIVES This study sought to evaluate the relationships between Lp(a) particle concentration and OxPLs associ-ated with apolipoprotein B (OxPL-apoB) or apolipoprotein(a) (OxPL-apo[a]) with angiographic CAD and cardiovascular outcomes.METHODS Among 1,098 participants referred for coronary angiography in the CASABLANCA (Catheter Sampled Blood Archive in Cardiovascular Diseases) study, Lp(a), OxPL-apoB, and OxPL-apo(a) were measured. Logistic regression esti-mated the risk of multivessel coronary stenoses by Lp(a)-related biomarker level. Cox proportional hazards regression estimated the risk of major adverse cardiovascular events (MACEs) (coronary revascularization, nonfatal myocardial infarction, nonfatal stroke, and cardiovascular death) in follow-up.RESULTS Median Lp(a) was 26.45 nmol/L (IQR: 11.39-89.49 nmol/L). Lp(a), OxPL-apoB, and OxPL-apo(a) were highly correlated (Spearman R $0.91 for all pairwise combinations). Lp(a) and OxPL-apoB were associated with multivessel CAD. Odds of multivessel CAD per doubling of Lp(a), OxPL-apoB, and OxPL-apo(a) were 1.10 (95% CI: 1.03-1.18; P = 0.006), 1.18 (95% CI: 1.03-1.34; P = 0.01), and 1.07 (95% CI: 0.99-1.16; P = 0.07), respectively. All biomarkers were associated with cardiovascular events. HRs for MACE per doubling of Lp(a), OxPL-apoB, and OxPL-apo(a) were 1.08 (95% CI: 1.03-1.14; P = 0.001), 1.15 (95% CI: 1.05-1.26; P = 0.004), and 1.07 (95% CI: 1.01-1.14; P = 0.02), respectively.CONCLUSIONS In patients undergoing coronary angiography, Lp(a) and OxPL-apoB are associated with multivessel CAD. Lp(a), OxPL-apoB, and OxPL-apo(a) are associated with incident cardiovascular events. (Catheter Sampled Blood Archive in Cardiovascular Diseases [CASABLANCA]; NCT00842868) (J Am Coll Cardiol 2023;81:1780-1792) (c) 2023 by the American College of Cardiology Foundation.
引用
收藏
页码:1780 / 1792
页数:13
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