作者
Esra D Gumuser, Art Schuermans, So Mi Jemma Cho, Zachary A Sporn, Md Mesbah Uddin, Kaavya Paruchuri, Tetsushi Nakao, Zhi Yu, Sara Haidermota, Whitney Hornsby, Lachelle D Weeks, Abhishek Niroula, Siddhartha Jaiswal, Peter Libby, Benjamin L Ebert, Alexander G Bick, Pradeep Natarajan, Michael C Honigberg
发表日期
2023/5/23
期刊
Journal of the American College of Cardiology
卷号
81
期号
20
页码范围
1996-2009
出版商
American College of Cardiology Foundation
简介
Background
Clonal hematopoiesis of indeterminate potential (CHIP)—the age-related clonal expansion of blood stem cells with leukemia-associated mutations—is a novel cardiovascular risk factor. Whether CHIP remains prognostic in individuals with established atherosclerotic cardiovascular disease (ASCVD) is less clear.
Objectives
This study tested whether CHIP predicts adverse outcomes in individuals with established ASCVD.
Methods
Individuals aged 40 to 70 years from the UK Biobank with established ASCVD and available whole-exome sequences were analyzed. The primary outcome was a composite of ASCVD events and all-cause mortality. Associations of any CHIP (variant allele fraction ≥2%), large CHIP clones (variant allele fraction ≥10%), and the most commonly mutated driver genes (DNMT3A, TET2, ASXL1, JAK2, PPM1D/TP53 [DNA damage repair genes], and SF3B1/SRSF2/U2AF1 …
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