Impact of Elevated Lipoprotein A on Clinical Outcomes in Patients Undergoing Percutaneous Coronary Intervention: A

Tanya Sinha1, Manisha Guntha2, Abshiro H Mayow3

  • 1Internal Medicine, Tribhuvan University, Kathmandu, NPL.

Cureus
|June 25, 2024
PubMed

Insights

Elevated Lipoprotein(a) (Lp(a)) levels significantly increase the risk of major adverse cardiovascular events (MACE) and mortality after percutaneous coronary intervention (PCI). Targeting Lp(a) may reduce residual cardiovascular risk in these patients.

Area of Science:

  • Cardiology
  • Genetics
  • Preventive Medicine

Background:

  • Lipoprotein(a) (Lp(a)) is an inherited particle linked to atherosclerotic cardiovascular disease risk.
  • The specific impact of elevated Lp(a) on outcomes following percutaneous coronary intervention (PCI) requires further clarification.

Purpose of the Study:

  • To evaluate the association between elevated Lp(a) levels and major adverse cardiovascular events (MACE) and other outcomes in patients undergoing PCI.
  • To synthesize current evidence on Lp(a) and post-PCI cardiovascular events.

Main Methods:

  • Systematic literature search of Embase, MEDLINE/PubMed, and Web of Science (2015-2024).
  • Inclusion of 15 studies with 45,059 patients comparing outcomes based on Lp(a) levels.
  • Meta-analysis of risk ratios (RRs) using a random-effect model for MACE, mortality, myocardial infarction, stroke, and revascularization.

Main Results:

  • Elevated Lp(a) was significantly associated with a higher risk of MACE (RR 1.38).
  • Increased risks were observed for all-cause mortality (RR 1.26), cardiovascular death (RR 1.58), myocardial infarction (RR 1.44), revascularization (RR 1.38), and stroke (RR 1.18).
  • Considerable heterogeneity was noted for some outcomes.

Conclusions:

  • Elevated Lp(a) levels predict worse cardiovascular outcomes post-PCI.
  • Higher rates of MACE, mortality, and recurrent ischemic events are linked to elevated Lp(a).
  • Therapeutic strategies targeting Lp(a) reduction could mitigate residual cardiovascular risk in this population.

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