Genome‐Wide Association Study of Cardiovascular Resilience Identifies Protective Variation in the CETP Gene

Author:

Yu Chenglong1ORCID,Bakshi Andrew1ORCID,Watts Gerald F.23ORCID,Renton Alan E.4,Fulton‐Howard Brian4ORCID,Goate Alison M.4ORCID,Natarajan Pradeep567ORCID,Chasman Daniel I.8ORCID,Robman Liubov19ORCID,Woods Robyn L.1ORCID,Guymer Robyn9ORCID,Wolfe Rory1ORCID,Thao Le Thi Phuong1ORCID,McNeil John J.1ORCID,Tonkin Andrew M.1ORCID,Nicholls Stephen J.110,Lacaze Paul1ORCID

Affiliation:

1. School of Public Health and Preventive Medicine Monash University Melbourne VIC Australia

2. School of Medicine University of Western Australia Perth WA Australia

3. Lipid Disorders Clinic, Cardiometabolic Service, Department of Cardiology Royal Perth Hospital Perth WA Australia

4. Department of Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai New York NY

5. Cardiovascular Research Center and Center for Genomic Medicine Massachusetts General Hospital Boston MA

6. Program in Population and Medical Genetics and the Cardiovascular Disease Initiative Broad Institute of Harvard and MIT Cambridge MA

7. Department of Medicine Harvard Medical School Boston MA

8. Preventive Medicine Division, Brigham and Women’s Hospital Harvard Medical School Boston MA

9. Centre for Eye Research Australia The University of Melbourne, Royal Victorian Eye and Ear Hospital Melbourne VIC Australia

10. Monash Cardiovascular Research Centre, Victorian Heart Institute Monash University Clayton VIC Australia

Abstract

Background The risk of atherosclerotic cardiovascular disease (ASCVD) increases sharply with age. Some older individuals, however, remain unaffected despite high predicted risk. These individuals may carry cardioprotective genetic variants that contribute to resilience. Our aim was to assess whether asymptomatic older individuals without prevalent ASCVD carry cardioprotective genetic variants that contribute to ASCVD resilience. Methods and Results We performed a genome‐wide association study using a 10‐year predicted ASCVD risk score as a quantitative trait, calculated only in asymptomatic older individuals aged ≥70 years without prevalent ASCVD. Our discovery genome‐wide association study of N=12 031 ASCVD event‐free individuals from the ASPREE (Aspirin in Reducing Events in the Elderly) trial identified 2 independent variants, rs9939224 ( P <5×10 −8 ) and rs56156922 ( P <10 −6 ), in the CETP (cholesteryl ester transfer protein) gene. The CETP gene is a regulator of plasma high‐density lipoprotein cholesterol, low‐density lipoprotein cholesterol, and lipoprotein(a) levels, and it is a therapeutic drug target. The associations were replicated in the UK Biobank (subpopulation of N=13 888 individuals aged ≥69 years without prevalent ASCVD). Carriers of the identified CETP variants (versus noncarriers) had higher plasma high‐density lipoprotein cholesterol levels, lower plasma low‐density lipoprotein cholesterol levels, and reduced risk of incident ASCVD events during follow‐up. Expression quantitative trait loci analysis predicted the identified CETP variants reduce CETP gene expression across various tissues. Previously reported associations between genetic CETP inhibition and increased risk of age‐related macular degeneration were not observed among the 3917 ASPREE trial participants with retinal imaging and genetic data available. Conclusions Common genetic variants in the CETP gene region are associated with cardiovascular resilience during aging. Registration URL: https://www.clinicaltrials.gov ; Unique identifier: NCT01038583.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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