Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2025 Jul;106(1):64-72.
doi: 10.1002/ccd.31363. Epub 2024 Dec 27.

Coronary Plaque Characteristics Assessed by Optical Coherence Tomography and Plasma Lipoprotein(a) Levels in Patients With Acute Coronary Syndrome

Affiliations
Observational Study

Coronary Plaque Characteristics Assessed by Optical Coherence Tomography and Plasma Lipoprotein(a) Levels in Patients With Acute Coronary Syndrome

Francesca Maria Di Muro et al. Catheter Cardiovasc Interv. 2025 Jul.

Abstract

Background: Lipoprotein(a) [Lp(a)] is associated with increased cardiovascular risk, but its influence on plaque characteristics at optical coherence tomography (OCT) evaluation is not fully understood.

Aims: This study seeks to explore the impact of Lp(a) levels on plaque morphology as assessed by OCT in a very high-risk subset of patients.

Methods: Consecutive patients admitted for acute coronary syndrome (ACS) and undergoing OCT-guided percutaneous coronary intervention (PCI) at a large tertiary care center between 2019 and 2022 were deemed eligible for the current analysis. The overall population was categorized into two subgroups according to baseline Lp(a) levels: (1) lower Lp(a) (Lp(a) ≤ 300 mg/L) and (2) elevated Lp(a) (Lp(a) 300 mg/L). Predictors of lipid-rich plaques were identified using multivariable logistic regression with stepwise selection of candidate covariates.

Results: A total of 202 patients were included in this study. OCT findings revealed that patients with elevated Lp(a) had a higher prevalence of lipid-rich plaques, a significantly greater mean lipid arc, along with increased macrophage infiltration and thin-cap fibroatheroma (TCFA). In contrast, calcific plaque prevalence was higher in the lower Lp(a) group. Multivariable regression analysis identified low-density lipoprotein cholesterol ≥ 70 mg/dL, and elevated Lp(a) as strong predictors of lipid-rich plaques at OCT.

Conclusion: In this observational study including ACS patients undergoing OCT-guided PCI, those with elevated Lp(a) levels exhibited a higher prevalence of lipid-rich plaques, increased macrophage infiltration, and TCFA, thereby indicating a more vulnerable plaque phenotype. Additionally, elevated Lp(a) levels and LDL-C levels ≥ 70 mg/dL were each independently associated with lipid enrichment of coronary plaques. These findings suggest Lp(a), beyond other well-known risk factors, as a key marker for risk stratification, potentially informing optimal medical management strategies.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Case examples of a lipid‐rich plaque with a minor fold‐over artifact(*) in panel A, a lipid‐rich plaque with thin‐cap fibroatheroma (arrow) in panel B, and macrophage infiltration in panel C at OCT assessment in ACS patients undergoing PCI. Abbreviations: ACS, acute coronary syndrome; Lp(a), lipoprotein a; OCT, optical coherence tomography; PCI, percutaneous coronary intervention. [Color figure can be viewed at wileyonlinelibrary.com]
Central Illustration 1
Central Illustration 1
Coronary plaque characteristics assessed by optical coherence tomography and plasma lipoprotein(a) levels in patients with acute coronary syndrome. Panel (A) shows the patient inclusion flow diagram, considering the selection criteria applied to all ACS patients undergoing OCT‐guided PCI at a large tertiary care center between 2019 and 2022, stratified by Lp(a) levels. Panel (B) shows the prevalence of plaque characteristics at OCT evaluation in patients with Lp(a) < 300 mg/L and Lp(a)300  mg/dL. Abbreviations: ACS, acute coronary syndrome; Lp(a), lipoprotein a; OCT, optical coherence tomography; PCI, percutaneous coronary intervention. [Color figure can be viewed at wileyonlinelibrary.com]

References

    1. Timmis A., Kazakiewicz D., Townsend N., Huculeci R., Aboyans V., and Vardas P., “Global Epidemiology of Acute Coronary Syndromes,” Nature Reviews Cardiology 20, no. 11 (2023): 778–788, 10.1038/s41569-023-00884-0. - DOI - PubMed
    1. Steen D. L., Khan I., Andrade K., Koumas A., and Giugliano R. P., “Event Rates and Risk Factors for Recurrent Cardiovascular Events and Mortality in a Contemporary Post Acute Coronary Syndrome Population Representing 239 234 Patients During 2005 to 2018 in the United States,” Journal of the American Heart Association 11, no. 9 (2022): e022198, 10.1161/JAHA.121.022198. - DOI - PMC - PubMed
    1. Byrne R. A., Rossello X., Coughlan J. J., et al., “2023 ESC Guidelines for the Management of Acute Coronary Syndromes,” European Heart Journal 44, no. 38 (2023): 3720–3826, 10.1093/eurheartj/ehad191. - DOI - PubMed
    1. Gual M., Valverde J., Santalo M., Ferrer M., Gonzalez Freixa C., and Sionis A., “ACS Program. Improving Secondary Prevention in Patients Admitted Due to a Myocardial Infarction. First Year Experience,” European Journal of Preventive Cardiology 31, no. Suppl_1 (2024): zwae175.090, 10.1093/eurjpc/zwae175.090. - DOI
    1. Panattoni G., Monzo L., Gugliotta M., et al., “Optimal Management of Patients After Acute Coronary Syndrome,” European Heart Journal Supplements 25, no. Suppl_C (2023): C84–C89, 10.1093/eurheartjsupp/suad039. - DOI - PMC - PubMed

Publication types

MeSH terms

LinkOut - more resources