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Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias.
Schuermans, Art; Vlasschaert, Caitlyn; Nauffal, Victor; Cho, So Mi Jemma; Uddin, Md Mesbah; Nakao, Tetsushi; Niroula, Abhishek; Klarqvist, Marcus D R; Weeks, Lachelle D; Lin, Amy E; Saadatagah, Seyedmohammad; Lannery, Kim; Wong, Megan; Hornsby, Whitney; Lubitz, Steven A; Ballantyne, Christie; Jaiswal, Siddhartha; Libby, Peter; Ebert, Benjamin L; Bick, Alexander G; Ellinor, Patrick T; Natarajan, Pradeep; Honigberg, Michael C.
Afiliação
  • Schuermans A; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, 75 Ames St., Cambridge, MA 02142, USA.
  • Vlasschaert C; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA.
  • Nauffal V; Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium.
  • Cho SMJ; Department of Medicine, Queens University, Kingston, ON, Canada.
  • Uddin MM; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, 75 Ames St., Cambridge, MA 02142, USA.
  • Nakao T; Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Niroula A; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, 75 Ames St., Cambridge, MA 02142, USA.
  • Klarqvist MDR; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA.
  • Weeks LD; Integrative Research Center for Cerebrovascular and Cardiovascular Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • Lin AE; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, 75 Ames St., Cambridge, MA 02142, USA.
  • Saadatagah S; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA.
  • Lannery K; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, 75 Ames St., Cambridge, MA 02142, USA.
  • Wong M; Cardiovascular Research Center and Center for Genomic Medicine, Massachusetts General Hospital, 185 Cambridge St., Boston, MA 02114, USA.
  • Hornsby W; Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Lubitz SA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Ballantyne C; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, 75 Ames St., Cambridge, MA 02142, USA.
  • Jaiswal S; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Libby P; Department of Laboratory Medicine, Lund University, Lund, Sweden.
  • Ebert BL; Data Sciences Platform, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
  • Bick AG; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Ellinor PT; Division of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Natarajan P; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Honigberg MC; Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
Eur Heart J ; 45(10): 791-805, 2024 Mar 07.
Article em En | MEDLINE | ID: mdl-37952204
ABSTRACT
BACKGROUND AND

AIMS:

Clonal haematopoiesis of indeterminate potential (CHIP), the age-related expansion of blood cells with preleukemic mutations, is associated with atherosclerotic cardiovascular disease and heart failure. This study aimed to test the association of CHIP with new-onset arrhythmias.

METHODS:

UK Biobank participants without prevalent arrhythmias were included. Co-primary study outcomes were supraventricular arrhythmias, bradyarrhythmias, and ventricular arrhythmias. Secondary outcomes were cardiac arrest, atrial fibrillation, and any arrhythmia. Associations of any CHIP [variant allele fraction (VAF) ≥ 2%], large CHIP (VAF ≥10%), and gene-specific CHIP subtypes with incident arrhythmias were evaluated using multivariable-adjusted Cox regression. Associations of CHIP with myocardial interstitial fibrosis [T1 measured using cardiac magnetic resonance (CMR)] were also tested.

RESULTS:

This study included 410 702 participants [CHIP n = 13 892 (3.4%); large CHIP n = 9191 (2.2%)]. Any and large CHIP were associated with multi-variable-adjusted hazard ratios of 1.11 [95% confidence interval (CI) 1.04-1.18; P = .001] and 1.13 (95% CI 1.05-1.22; P = .001) for supraventricular arrhythmias, 1.09 (95% CI 1.01-1.19; P = .031) and 1.13 (95% CI 1.03-1.25; P = .011) for bradyarrhythmias, and 1.16 (95% CI, 1.00-1.34; P = .049) and 1.22 (95% CI 1.03-1.45; P = .021) for ventricular arrhythmias, respectively. Associations were independent of coronary artery disease and heart failure. Associations were also heterogeneous across arrhythmia subtypes and strongest for cardiac arrest. Gene-specific analyses revealed an increased risk of arrhythmias across driver genes other than DNMT3A. Large CHIP was associated with 1.31-fold odds (95% CI 1.07-1.59; P = .009) of being in the top quintile of myocardial fibrosis by CMR.

CONCLUSIONS:

CHIP may represent a novel risk factor for incident arrhythmias, indicating a potential target for modulation towards arrhythmia prevention and treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Parada Cardíaca / Insuficiência Cardíaca Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Parada Cardíaca / Insuficiência Cardíaca Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article