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Review
. 2024 May 25;16(5):e61069.
doi: 10.7759/cureus.61069. eCollection 2024 May.

Impact of Elevated Lipoprotein A on Clinical Outcomes in Patients Undergoing Percutaneous Coronary Intervention: A Systematic Review and Meta-analysis

Affiliations
Review

Impact of Elevated Lipoprotein A on Clinical Outcomes in Patients Undergoing Percutaneous Coronary Intervention: A Systematic Review and Meta-analysis

Tanya Sinha et al. Cureus. .

Abstract

Lipoprotein(a) (Lp(a)) is an inherited lipoprotein particle associated with increased risk of atherosclerotic cardiovascular (CV) diseases. However, its impact on outcomes after percutaneous coronary intervention (PCI) remains unclear. The objective of this study was to assess the relationship between elevated Lp(a) levels and major adverse cardiovascular events (MACEs) and other outcomes in patients undergoing PCI. We systematically searched Embase, MEDLINE/PubMed, and Web of Science for studies published from 2015 to 2024 comparing CV outcomes between patients with elevated versus non-elevated Lp(a) levels after PCI. Primary outcome was MACE. Secondary outcomes included all-cause mortality, CV mortality, stroke, myocardial infarction, and revascularization. Risk ratios (RRs) were pooled using a random-effect model. Fifteen studies with 45,059 patients were included. Patients with elevated Lp(a) had a significantly higher risk of MACE (RR 1.38, 95% confidence interval (CI) 1.23-1.56). Elevated Lp(a) was also associated with increased risks of all-cause death (RR 1.26), CV death (RR 1.58), myocardial infarction (RR 1.44), revascularization (RR 1.38), and stroke (RR 1.18). Heterogeneity was considerable for some outcomes. This meta-analysis demonstrates that elevated Lp(a) levels are associated with worse CV outcomes, including higher rates of MACE, mortality, and recurrent ischemic events in patients undergoing PCI. Novel therapeutic approaches specifically targeting Lp(a) reduction may help mitigate residual CV risk in this high-risk population.

Keywords: cardiovascular outcomes; lipoprotein (a); mortality; percutaneous coronary intervention; systematic review and meta-analysis.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. PRISMA flowchart of study selection
PRISMA: Preferred Reporting Items for Systematic reviews and Meta-Analyses
Figure 2
Figure 2. Effect of elevated Lp(a) on MACE
References: [12,15,19,21-26]

References

    1. Recent advances in treatment of coronary artery disease: role of science and technology. Kandaswamy E, Zuo L. Int J Mol Sci. 2018;19 - PMC - PubMed
    1. Percutaneous coronary revascularization: JACC historical breakthroughs in perspective. Serruys PW, Ono M, Garg S, et al. J Am Coll Cardiol. 2021;78:384–407. - PubMed
    1. Lipoprotein (a): truly a direct prothrombotic factor in cardiovascular disease? Boffa MB, Koschinsky ML. J Lipid Res. 2016;57:745–757. - PMC - PubMed
    1. A not-so-little role for lipoprotein(a) in the development of calcific aortic valve disease. Rogers MA, Aikawa E. Circulation. 2015;132:621–623. - PMC - PubMed
    1. Antisense oligonucleotides targeting apolipoprotein(a) in people with raised lipoprotein(a): two randomised, double-blind, placebo-controlled, dose-ranging trials. Viney NJ, van Capelleveen JC, Tsimikas S, et al. Lancet. 2016;388:2239–2253. - PubMed

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