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
Review
. 2021 Apr 1;32(2):112-116.
doi: 10.1097/MOL.0000000000000741.

The clinical applicability of polygenic risk scores for LDL-cholesterol: considerations, current evidence and future perspectives

Affiliations
Review

The clinical applicability of polygenic risk scores for LDL-cholesterol: considerations, current evidence and future perspectives

Arjen J Cupido et al. Curr Opin Lipidol. .

Abstract

Purpose of review: The current review describes the development, clinical relevance and potential caveats of polygenic risk scores (PRS) for LDL cholesterol (LDL-C).

Recent findings: In recent years, a large number of common variants have been shown to have a small effect on LDL-C levels. The aggregate effect of all of these variants on LDL-C levels can be captured in a PRS and an elevated number of LDL-C increasing common variants is considered to be a cause of high LDL-C levels in patients with familial hypercholesterolemia (FH) without a large effect, rare mutation. PRS do not only serve as a tool in diagnostics, but are also helpful in cardiovascular disease (CVD) risk prediction. Moreover, PRS modulate CVD risk even in patients without a monogenic FH. However, future larger scale PRS directly aimed at CVD risk may serve as more sensitive tools to identify individuals with severely increased CVD risk.

Summary: LDL-C PRS help explain part of hypercholesterolemia in a proportion of dyslipidemic patients that do not have monogenic FH. Nevertheless, the CVD risk conferred by current PRS does not appear to match that of monogenic FH. LDL-C PRS are currently not widely used in clinical care.

PubMed Disclaimer

Conflict of interest statement

There are no conflicts of interest.

Figures

Box 1
Box 1
no caption available

References

    1. Buniello A, Macarthur JAL, Cerezo M, et al. . The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019. Nucleic Acids Res 2019; 47:D1005–D1012. - PMC - PubMed
    1. Klarin D, Damrauer SM, Cho K, et al. . Genetics of blood lipids among ∼300,000 multiethnic participants of the Million Veteran Program. Nat Genet 2018; 50:1514–1523. - PMC - PubMed
    1. Boyle EA, Li YI, Pritchard JK. An expanded view of complex traits: from polygenic to omnigenic. Cell 2017; 169:1177–1186. - PMC - PubMed
    1. Kathiresan S, Melander O, Guiducci C, et al. . Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet 2008; 40:189–197. - PMC - PubMed
    1. Kathiresan S, Willer CJ, Peloso GM, et al. . Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 2009; 41:56–65. - PMC - PubMed

Publication types

Substances