학술논문

Rare Genetic Variants Associated With Myocardial Fibrosis: Multi-Ethnic Study of Atherosclerosis
Document Type
article
Source
Subject
Biomedical and Clinical Sciences
Cardiovascular Medicine and Haematology
Atherosclerosis
Cardiovascular
Prevention
Clinical Research
Genetics
Heart Disease
Aetiology
2.1 Biological and endogenous factors
Good Health and Well Being
cardiomyopathy
genetics
fibrosis
magnetic resonance imaging
T1
interstitial
rare
Cardiovascular medicine and haematology
Language
Abstract
BackgroundRare pathogenic variants in cardiomyopathy (CM) genes can predispose to cardiac remodeling or fibrosis. We studied the carrier status for such variants in adults without clinical cardiovascular disease (CVD) in whom cardiac MRI (CMR)-derived measures of myocardial fibrosis were obtained in the Multi-Ethnic Study of Atherosclerosis (MESA).ObjectivesTo identify CM-associated pathogenic variants and assess their relative prevalence in participants with extensive myocardial fibrosis by CMR.MethodsMESA whole-genome sequencing data was evaluated to capture variants in CM-associated genes (n = 82). Coding variants with a frequency of