Key result
Elevated lipoprotein(a) is associated with non-calcified or mixed coronary plaque morphology, accelerated plaque progression, and increased risk of high-risk plaque features on coronary imaging.
Why the study?
Does coronary artery imaging improve cardiovascular risk stratification in individuals with elevated Lipoprotein(a)?
Does coronary artery imaging improve cardiovascular risk stratification in individuals with elevated Lipoprotein(a)?
Answers are grounded in this paper and cite their sources.
Coronary imaging demonstrates that elevated Lp(a) is linked to high-risk plaque features and accelerated progression, highlighting its potential utility in risk stratification.
Purpose of Review Summarize current literature on the use of coronary artery imaging modalities in examining the atherosclerotic and arterial inflammatory manifestations of elevated lipoprotein(a) [Lp(a)]. Evaluate the evolving role of coronary imaging in risk stratification and treatment decisions. Recent Findings While Lp(a) and calcium scoring (CAC) are independently associated with cardiovascular risk, Lp(a) is associated with CAC incidence and progression. Lp(a) is associated with greater plaque prevalence, multivessel disease, and high-risk morphologies, while also being linked to accelerated progression of mixed and lipid-rich plaque by coronary CT angiography. Intravascular imaging modalities further show associations between Lp(a) and thin-cap fibroatheroma, lipid-rich plaque, percent atheroma volume, and plaque progression. Summary Lp(a) is associated with non-calcified or mixed coronary plaque morphology and progression, as well as increased risk of high-risk plaque features. While additional research is needed, current literature suggests that coronary imaging may be an important tool in cardiovascular risk stratification for individuals with elevated Lp(a).
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Savides et al. (2026) conducted a review in Elevated lipoprotein(a) and cardiovascular risk. Coronary artery imaging was evaluated. Elevated lipoprotein(a) is associated with non-calcified or mixed coronary plaque morphology, accelerated plaque progression, and increased risk of high-risk plaque features on coronary imaging.
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