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Epidemiology

LipidCardio study of 975 angiography patients finds Lp(a) above 150 nmol/L doubles chronic total occlusion rates and lifts Gensini scores (Eur J Prev Cardiol 2024)

Original title: Impact of elevated lipoprotein(a) on coronary artery disease phenotype and severity

Eur J Prev Cardiol · · 7

Leistner DM, Laguna-Fernandez A, Haghikia A, Abdelwahed YS, Schatz AS, Erbay A, Roehle R, Fonseca AF, Ferber P, Landmesser U

This non-interventional, cross-sectional LipidCardio study included 975 patients (mean age 69.5 years, 70.1% male, 97.5% Caucasian) undergoing coronary angiography at a tertiary centre between October 2016 and March 2018, with Lp(a) stratified from under 65 nmol/L (72.9%) up to 150 nmol/L or above (12.9%). Compared with patients with Lp(a) below 65 nmol/L, those at or above 150 nmol/L had significantly higher rates of prior coronary artery disease (48.4% vs. 62.7%), prior revascularisation (39.1% vs. 51.6%), prior bypass surgery (6.0% vs. 15.1%), vessels with lesions (68.5% vs. 81.3%), diffusely narrowed vessels (10.9% vs. 16.5%), and chronic total occlusion (14.3% vs. 25.2%, all P less than or equal to 0.03), along with higher median SYNTAX-I (3.0 vs. 5.5) and Gensini (10.0 vs. 16.0) severity scores (both P less than or equal to 0.01). Elevated Lp(a) is associated with a more extensive and severe presentation of coronary artery disease in this real-world angiography population, reinforcing the case for incorporating Lp(a) awareness into the clinical management of CAD patients.

Read the paper (DOI)PubMed

Original abstract

Aims: A thorough characterization of the relationship between elevated lipoprotein(a) [Lp(a)] and coronary artery disease (CAD) is lacking. This study aimed to quantitatively assess the association of increasing Lp(a) levels and CAD severity in a real-world population.

Methods And Results: This non-interventional, cross-sectional, LipidCardio study included patients aged ≥21 years undergoing angiography (October 2016-March 2018) at a tertiary cardiology centre, who have at least one Lp(a) measurement. The association between Lp(a) and CAD severity was determined by synergy between PCI with taxus and cardiac surgery (SYNTAX)-I and Gensini scores and angiographic characteristics. Overall, 975 patients (mean age: 69.5 years) were included; 70.1% were male, 97.5% had Caucasian ancestry, and 33.2% had a family history of premature atherosclerotic cardiovascular disease. Median baseline Lp(a) level was 19.3 nmol/L. Patients were stratified by baseline Lp(a): 72.9% had < 65 nmol/L, 21.0% had ≥100 nmol/L, 17.2% had ≥125 nmol/L, and 12.9% had ≥150 nmol/L. Compared with the normal (Lp(a) < 65 nmol/L) group, elevated Lp(a) groups (e.g. ≥ 150 nmol/L) had a higher proportion of patients with prior CAD (48.4% vs. 62.7%; P < 0.01), prior coronary revascularization (39.1% vs. 51.6%; P = 0.01), prior coronary artery bypass graft (6.0% vs. 15.1%; P < 0.01), vessel(s) with lesions (68.5% vs. 81.3%; P = 0.03), diffusely narrowed vessels (10.9% vs. 16.5%; P = 0.01) or chronic total occlusion lesions (14.3% vs. 25.2%; P < 0.01), and higher median SYNTAX-I (3.0 vs. 5.5; P = 0.01) and Gensini (10.0 vs. 16.0; P < 0.01) scores.

Conclusion: Elevated Lp(a) was associated with a more severe presentation of CAD. Awareness of Lp(a) levels in patients with CAD may have implications in their clinical management.

epidemiology

Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.