Scientific Sessions 2025  /  Population-based Genomic Risk Prediction for Cardiovascular Disease 2  /  Population Screening for Polygenic Risk Identifies and Prevents More Cases of Coronary Artery Disease Than Screening for FH
Logo

American Heart Association

  78
  0

Final ID: Mo4057

Population Screening for Polygenic Risk Identifies and Prevents More Cases of Coronary Artery Disease Than Screening for FH

Abstract Body (Do not enter title and authors here):
Background:
Due to the availability of effective lipid-lowering therapies, familial hypercholesterolemia (FH) case finding is adopted by many healthcare systems. In parallel, polygenic risk scores (PRS) have emerged as a powerful tool for capturing the effect of common genetic variants associated with CAD.

Research Question:
What proportion of individuals at high PRS for CAD exhibit equivalent risk compared to FH variant carriers, and what are the potential clinical benefits of treating these individuals with statins.

Methods:
We analyzed data from the UK Biobank, identifying FH carriers via whole-exome sequencing and defining polygenic risk using a CAD PRS. Incident CAD events in statin-naive individuals were compared between FH carriers and individuals with high PRS. Number-needed-to-treat (NNT) with statins and number needed to screen (NNS) were calculated to assess therapeutic impact in high PRS individuals.

Results:
The top 8% of the PRS distribution exhibited comparable or higher CAD risk than FH carriers. This high-PRS group accounted for between 18 and 29 times more CAD events than FH carriers, depending on age. In the untreated high PRS group the rate of CAD events was 10.28 per 1000 person years (9.01 - 11.67) compared to 6.78 per 1000 person years (5.39 - 8.42) in the treated high PRS group, representing a relative risk reduction (RRR) of 0.34 (0.15 - 0.49). In the median PRS group, the rate of CAD events was 5.28 per 1000 persons (4.67 - 5.94) compared to 3.93 per 1000 person years (3.21 - 4.75) in the treated group, representing a RRR of 0.26 (0.07 - 0.41). The NNT in the high PRS group was 286 compared to 741 in the median PRS group, indicating that statins were roughly 2.6 fold more effective, after matching on clinical risk factors. The NNT (286) for statins in the high PRS group is similar to literature based estimates for statin treatment in FH (222) but the number needed to screen is approximately 21 fold higher for FH than for high PRS.

Conclusion:
In the population, screening for high CAD PRS individuals will prevent more CAD cases than screening for FH. This is because high PRS individuals are much more prevalent than FH individuals and have enhanced therapeutic benefit from statin treatment (compared to those without high PRS). The polygenic component of CAD is a major, treatable risk factor that is not routinely evaluated in prevention programs, despite a growing body of evidence that this can be implemented easily into clinical practice.
  • Harrison, Seamus  ( Genomics Ltd , Oxford , United Kingdom )
  • Riveros-mckay, Fernando  ( Genomics Ltd , Oxford , United Kingdom )
  • Thompson, Deborah  ( Genomics Ltd , Oxford , United Kingdom )
  • Neogi, Arpita  ( Genomics Ltd , Oxford , United Kingdom )
  • Weale, Michael  ( Genomics Ltd , Oxford , United Kingdom )
  • Plagnol, Vincent  ( Genomics Ltd , Oxford , United Kingdom )
  • Donnelly, Peter  ( Genomics Ltd , Oxford , United Kingdom )
    • Author Disclosures:
    Seamus Harrison: DO NOT have relevant financial relationships | Fernando Riveros-Mckay: No Answer | Deborah Thompson: No Answer | Arpita Neogi: DO have relevant financial relationships ; Employee:Genomics:Active (exists now) | Michael Weale: DO have relevant financial relationships ; Employee:Genomics Ltd:Active (exists now) ; Royalties/Patent Beneficiary:Genomics Ltd:Active (exists now) | Vincent Plagnol: No Answer | Peter Donnelly: DO have relevant financial relationships ; Employee:Genomics Ltd:Active (exists now) ; Other (please indicate in the box next to the company name):Biometrika Trust:Active (exists now) ; Royalties/Patent Beneficiary:Peptide Groove LLP:Active (exists now) ; Individual Stocks/Stock Options:Genomics Ltd:Active (exists now)
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:

Population-based Genomic Risk Prediction for Cardiovascular Disease 2

Monday, 11/10/2025 , 01:00PM - 02:00PM

Abstract Poster Board Session

More abstracts on this topic:
A Focus for Improvement - Factors for Lab Adherence in a Pediatric Preventive Cardiology Program

Holsinger Hunter, Porterfield Ronna, Taylor Makenna, Dresbach Bethany, Seipel Brittany, Igwe Chukwuemeka, Alvarado Chance, Tran Andrew

A Novel Machine Learning Strategy to Integrate Multi-Omics Data and Detect Genomic Loci and Gene-Environment Interactions for LDL Cholesterol

Li Changwei, Zhang Ruiyuan, Sun Yixi, Chen Jing, Wang Tao, Bazzano Lydia, Kelly Tanika, He Jiang

More abstracts from these authors:
Adding a polygenic risk score to the PREVENT clinical risk tool significantly improves cardiovascular risk prediction

Euesden Jack, Absher Devin, Iribarren Carlos, Riveros-mckay Fernando, Rana Jamal, Rowell Sarah, Neogi Arpita, Harrison Seamus, Weale Michael, Donnelly Peter

You have to be authorized to contact abstract author. Please, Login
Not Available