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Clonal haematopoiesis is associated with major adverse cardiovascular events in patients with hypertrophic cardiomyopathy.
- Source :
-
European journal of heart failure [Eur J Heart Fail] 2024 Oct; Vol. 26 (10), pp. 2193-2202. Date of Electronic Publication: 2024 Aug 01. - Publication Year :
- 2024
-
Abstract
- Aims: The heterogeneous phenotype of hypertrophic cardiomyopathy (HCM) is still not fully understood. Clonal haematopoiesis (CH) is emerging as a cardiovascular risk factor potentially associated with adverse clinical events. The prevalence, phenotype and outcomes related to CH in HCM patients were evaluated.<br />Methods and Results: Patients with HCM and available biospecimens from the Peter Munk Cardiac Centre Cardiovascular Biobank were subjected to targeted sequencing for 35 myeloid genes associated with CH. CH prevalence, clinical characteristics, morphological phenotypes assessed by echocardiogram and cardiac magnetic resonance and outcomes were assessed. All patients were evaluated for a 71-plex cytokines/chemokines, troponin I and B-type natriuretic peptide analysis. Major adverse cardiovascular events (MACE) were defined as appropriate implantable cardioverter-defibrillator shock, stroke, cardiac arrest, orthotopic heart transplant and death. Among the 799 patients, CH was found in 183 (22.9%) HCM patients with sarcomeric germline mutations. HCM patients with CH were more symptomatic and with a higher burden of fibrosis than those without CH. CH was associated with MACE in those HCM patients with sarcomeric germline mutations (adjusted hazard ratio [HR] 6.89, 95% confidence interval [CI] 1.78-26.6; p = 0.005), with the highest risk among those that had DNMT3A, TET2 and ASXL1 mutations (adjusted HR 5.76, 95% CI 1.51-21.94; p = 0.010). Several cytokines (IL-1ra, IL-6, IL-17F, TGFα, CCL21, CCL1, CCL8, and CCL17), and troponin I were upregulated in gene-positive HCM patients with CH.<br />Conclusions: These results indicate that CH in patients with HCM is associated with worse clinical outcomes. In the absence of CH, gene-positive patients with HCM have lower rates of MACE.<br /> (© 2024 The Author(s). European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.)
- Subjects :
- Humans
Male
Female
Middle Aged
DNA Methyltransferase 3A
Repressor Proteins genetics
Proto-Oncogene Proteins genetics
DNA (Cytosine-5-)-Methyltransferases genetics
DNA-Binding Proteins genetics
Troponin I blood
Aged
Echocardiography
Phenotype
Cytokines genetics
Natriuretic Peptide, Brain blood
Mutation
Adult
Risk Factors
Heart Arrest etiology
Dioxygenases
Cardiomyopathy, Hypertrophic genetics
Cardiomyopathy, Hypertrophic complications
Cardiomyopathy, Hypertrophic physiopathology
Clonal Hematopoiesis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0844
- Volume :
- 26
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- European journal of heart failure
- Publication Type :
- Academic Journal
- Accession number :
- 39091134
- Full Text :
- https://doi.org/10.1002/ejhf.3408