» Articles » PMID: 39682665

Lipoprotein(a) As a Risk Factor for Recurrent Acute Myocardial Infarction and Mortality: Insights from Routine Clinical Practice

Overview
Specialty Radiology
Date 2024 Dec 17
PMID 39682665
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Lipoprotein(a) [Lp(a)] is a well-established risk factor for incident atherosclerotic cardiovascular (CV) disease. However, evidence regarding its association with recurrent events is limited. To address this gap, we conducted a retrospective analysis of routine clinical data, focusing on patients hospitalized for acute myocardial infarction (AMI) between 2000 and 2022 with available admission Lp(a) results.

Methods: Patients were stratified into three groups based on their Lp(a) level (≤50 mg/dL, 51-90 mg/dL, and >90 mg/dL). A multivariable-adjusted Cox regression analysis was performed to assess the associations of Lp(a) with recurrent AMI, CV mortality, and all-cause mortality.

Results: A total of 2248 patients (31.5% women), with a mean age of 64.7 ± 12.2 years, were retrospectively followed until 31 December 2022, or death. The multivariable-adjusted hazard ratios (HRs) for recurrent AMI were 1.01 ( = 0.921) for levels 51-90 mg/dL and 1.51 ( = 0.013) for levels > 90 mg/dL, compared with levels ≤ 50 mg/dL. The corresponding HRs for CV mortality were 1.13 ( = 0.300) and 1.14 ( = 0.348), and those for all-cause mortality were 1.09 ( = 0.310) and 1.20 ( = 0.090), respectively. Stratification by sex and age revealed a significant association of Lp(a) with recurrent AMI only in women aged > 65 years, with adjusted HRs of 2.34 ( = 0.013) for levels 51-90 mg/dL and 3.94 ( < 0.001) for levels > 90 mg/dL, compared with levels ≤ 50 mg/dL.

Conclusions: In the presented study, Lp(a) was associated with a significantly higher risk of recurrent AMI only in women aged > 65 years with Lp(a) levels > 50 mg/dL. We found no significant associations between Lp(a) and CV or all-cause mortality.

References
1.
Gurdasani D, Sjouke B, Tsimikas S, Hovingh G, Luben R, Wainwright N . Lipoprotein(a) and risk of coronary, cerebrovascular, and peripheral artery disease: the EPIC-Norfolk prospective population study. Arterioscler Thromb Vasc Biol. 2012; 32(12):3058-65. PMC: 4210842. DOI: 10.1161/ATVBAHA.112.255521. View

2.
Kamstrup P, Tybjaerg-Hansen A, Nordestgaard B . Elevated lipoprotein(a) and risk of aortic valve stenosis in the general population. J Am Coll Cardiol. 2013; 63(5):470-7. DOI: 10.1016/j.jacc.2013.09.038. View

3.
Wei D, Zhang X, Wang R, Zeng J, Zhang K, Yang J . Oxidized lipoprotein(a) increases endothelial cell monolayer permeability via ROS generation. Lipids. 2013; 48(6):579-86. DOI: 10.1007/s11745-013-3795-1. View

4.
ODonoghue M, Morrow D, Tsimikas S, Sloan S, Ren A, Hoffman E . Lipoprotein(a) for risk assessment in patients with established coronary artery disease. J Am Coll Cardiol. 2013; 63(6):520-7. PMC: 3945105. DOI: 10.1016/j.jacc.2013.09.042. View

5.
Erqou S, Kaptoge S, Perry P, Di Angelantonio E, Thompson A, White I . Lipoprotein(a) concentration and the risk of coronary heart disease, stroke, and nonvascular mortality. JAMA. 2009; 302(4):412-23. PMC: 3272390. DOI: 10.1001/jama.2009.1063. View