Assessment of practical applicability and clinical relevance of a commonly used LDL-C polygenic score in patients with severe hypercholesterolemia. (January 2022)

• Record Type: Journal Article
• Authors: Tromp, Tycho R.; Cupido, Arjen J.; Reeskamp, Laurens F.; Stroes, Erik S.G.; Hovingh, G. Kees; Defesche, Joep C.; Schmidt, Amand F.; Zuurbier, Linda
• Is Part Of: Atherosclerosis. Volume 340(2022)
• Page Start: 61
• Page End: 67
• Publication Date: 2022-01
• Subjects: LDL-Cholesterol -- Familial hypercholesterolemia -- Polygenic trait -- SNPs -- Cardiovascular disease -- Risk prediction; Arteriosclerosis -- Periodicals; Electronic journals; 616.136
• DOI: 10.1016/j.atherosclerosis.2021.10.015
• Languages: English
• ISSNs: 0021-9150

Abstract

Abstract: Background and aims: Low-density lipoprotein cholesterol (LDL-C) levels vary in patients with familial hypercholesterolemia (FH) and can be explained by a single deleterious genetic variant or by the aggregate effect of multiple, common small-effect variants that can be captured in a polygenic score (PS). We set out to investigate the contribution of a previously published PS to the inter-individual LDL-C variation and coronary artery disease (CAD) risk in patients with a clinical FH phenotype. Methods: First, in a cohort of 628 patients referred for genetic FH testing, we evaluated the distribution of a PS for LDL-C comprising 12 genetic variants. Next, we determined its association with coronary artery disease (CAD) risk using UK Biobank data. Results: The mean PS was higher in 533 FH-variant-negative patients (FH/M-) compared with 95 FH-variant carriers (1.02 vs 0.94, p < 0.001). 39% of all patients had a PS equal to the top 20% from a population-based reference cohort and these patients were less likely to carry an FH variant (OR 0.22, 95% CI 0.10–0.48) compared with patients in the lowest 20%. In UK Biobank data, the PS explained 7.4% of variance in LDL-C levels and was associated with incident CAD. Addition of PS to a prediction model using age and sex and LDL-C did not increase the c-statistic for predicting CAD risk. Conclusions: This 12-variant PS was higher in FH/M- patients and associated with incident CAD in UK Biobank data. However, the PS did not improve predictive accuracy when added to the readily available characteristics age, sex and LDL-C, suggesting limited discriminative value for CAD. Graphical abstract: Image 1 Highlights: Clinical familial hypercholesterolemia (FH) without monogenic cause may be explained by a polygenic background. A 12-variant polygenic score explains 7% of low-density lipoprotein cholesterol (LDL-C) variance in the general population. This score is modestly associated with incident coronary artery disease. This does not improve risk discrimination, suggesting little clinical benefit.