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Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias
DC Field | Value | Language |
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dc.date.accessioned | 2025-03-13T16:56:06Z | - |
dc.date.available | 2025-03-13T16:56:06Z | - |
dc.date.issued | 2024-03 | - |
dc.identifier.issn | 0195-668X | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/204223 | - |
dc.description.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. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Oxford University Press | - |
dc.relation.isPartOf | EUROPEAN HEART JOURNAL | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Atrial Fibrillation* | - |
dc.subject.MESH | Bradycardia | - |
dc.subject.MESH | Clonal Hematopoiesis | - |
dc.subject.MESH | Heart Arrest* | - |
dc.subject.MESH | Heart Failure* | - |
dc.subject.MESH | Humans | - |
dc.title | Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Others | - |
dc.contributor.googleauthor | Art Schuermans | - |
dc.contributor.googleauthor | Caitlyn Vlasschaert | - |
dc.contributor.googleauthor | Victor Nauffal | - |
dc.contributor.googleauthor | So Mi Jemma Cho | - |
dc.contributor.googleauthor | Md Mesbah Uddin | - |
dc.contributor.googleauthor | Tetsushi Nakao | - |
dc.contributor.googleauthor | Abhishek Niroula | - |
dc.contributor.googleauthor | Marcus D R Klarqvist | - |
dc.contributor.googleauthor | Lachelle D Weeks | - |
dc.contributor.googleauthor | Amy E Lin | - |
dc.contributor.googleauthor | Seyedmohammad Saadatagah | - |
dc.contributor.googleauthor | Kim Lannery | - |
dc.contributor.googleauthor | Megan Wong | - |
dc.contributor.googleauthor | Whitney Hornsby | - |
dc.contributor.googleauthor | Steven A Lubitz | - |
dc.contributor.googleauthor | Christie Ballantyne | - |
dc.contributor.googleauthor | Siddhartha Jaiswal | - |
dc.contributor.googleauthor | Peter Libby | - |
dc.contributor.googleauthor | Benjamin L Ebert | - |
dc.contributor.googleauthor | Alexander G Bick | - |
dc.contributor.googleauthor | Patrick T Ellinor | - |
dc.contributor.googleauthor | Pradeep Natarajan | - |
dc.contributor.googleauthor | Michael C Honigberg | - |
dc.identifier.doi | 10.1093/eurheartj/ehad670 | - |
dc.relation.journalcode | J00805 | - |
dc.identifier.eissn | 1522-9645 | - |
dc.identifier.pmid | 37952204 | - |
dc.subject.keyword | Aging | - |
dc.subject.keyword | Arrhythmia | - |
dc.subject.keyword | Atrial fibrillation | - |
dc.subject.keyword | Cardiac arrest | - |
dc.subject.keyword | Genomics | - |
dc.subject.keyword | Prevention | - |
dc.citation.volume | 45 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 791 | - |
dc.citation.endPage | 805 | - |
dc.identifier.bibliographicCitation | EUROPEAN HEART JOURNAL, Vol.45(10) : 791-805, 2024-03 | - |
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