Clonal Hematopoiesis Is Associated With Long-Term Adverse Outcomes Following Cardiac Surgery.

cardiac surgery clonal hematopoiesis heart failure inflammation survival

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
29 Aug 2024
Historique:
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: aheadofprint

Résumé

Cardiac surgery triggers sterile innate immune responses leading to postoperative complications. Clonal hematopoiesis (CH) is associated with short-term inflammation-mediated outcomes after cardiac surgery. The impact of CH on long-term postoperative outcomes remains unknown. In this cohort study, patients undergoing elective cardiac surgery were included from January 2017 to September 2019. Patients were screened for CH using a predefined gene panel of 19 genes. Recorded clinical events were all-cause death, major adverse cardiac and cerebral events including cardiovascular death, myocardial infarction or nonscheduled coronary revascularization, stroke, and hospitalization for acute heart failure. The primary study outcome was time to a composite criterion including all-cause mortality and major adverse cardiac and cerebral events. Among 314 genotyped patients (median age: 67 years; interquartile range 59-74 years), 139 (44%) presented with CH, based on a variant allelic frequency ≥1%. Carriers of CH had a higher proportion of patients with a history of atrial fibrillation (26% for CH versus 17% for non-CH carriers, In patients undergoing cardiac surgery, CH is frequent and associated with a 2-fold increased long-term risk for major adverse clinical outcomes. CH is a novel risk factor for long-term postcardiac surgery complications and might be useful to personalize management decisions. URL: https://www.clinicaltrials.gov; Unique identifier: NCT03376165.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac surgery triggers sterile innate immune responses leading to postoperative complications. Clonal hematopoiesis (CH) is associated with short-term inflammation-mediated outcomes after cardiac surgery. The impact of CH on long-term postoperative outcomes remains unknown.
METHODS AND RESULTS RESULTS
In this cohort study, patients undergoing elective cardiac surgery were included from January 2017 to September 2019. Patients were screened for CH using a predefined gene panel of 19 genes. Recorded clinical events were all-cause death, major adverse cardiac and cerebral events including cardiovascular death, myocardial infarction or nonscheduled coronary revascularization, stroke, and hospitalization for acute heart failure. The primary study outcome was time to a composite criterion including all-cause mortality and major adverse cardiac and cerebral events. Among 314 genotyped patients (median age: 67 years; interquartile range 59-74 years), 139 (44%) presented with CH, based on a variant allelic frequency ≥1%. Carriers of CH had a higher proportion of patients with a history of atrial fibrillation (26% for CH versus 17% for non-CH carriers,
CONCLUSIONS CONCLUSIONS
In patients undergoing cardiac surgery, CH is frequent and associated with a 2-fold increased long-term risk for major adverse clinical outcomes. CH is a novel risk factor for long-term postcardiac surgery complications and might be useful to personalize management decisions.
REGISTRATION BACKGROUND
URL: https://www.clinicaltrials.gov; Unique identifier: NCT03376165.

Identifiants

pubmed: 39206728
doi: 10.1161/JAHA.123.034255
doi:

Banques de données

ClinicalTrials.gov
['NCT03376165']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e034255

Auteurs

Sandro Ninni (S)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.
Department of Medicine and Research Center Montreal Heart Institute and Université de Montréal Montreal Canada.

Rocio Vicario (R)

Immunology Program Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center New York NY USA.

Augustin Coisne (A)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Eloise Woitrain (E)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Amine Tazibet (A)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Caitlin M Stewart (CM)

Division of Solid Tumor Oncology, Department of Medicine Memorial Sloan Kettering Cancer Center New York NY USA.

Luis A Diaz (LA)

Division of Solid Tumor Oncology, Department of Medicine Memorial Sloan Kettering Cancer Center New York NY USA.

James Robert White (JR)

Resphera Biosciences Baltimore MD USA.

Mohammed Koussa (M)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Henri Dubrulle (H)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Francis Juthier (F)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Marie Jungling (M)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

André Vincentelli (A)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Jean-Louis Edme (JL)

Université de Lille, EA 4483, IMPECS: IMPact of Environmental ChemicalS on Human Health, CHU Lille Lille France.

Stanley Nattel (S)

Department of Medicine and Research Center Montreal Heart Institute and Université de Montréal Montreal Canada.

Menno de Winther (M)

Department of Medical Biochemistry, Experimental Vascular Biology, Amsterdam Cardiovascular Sciences, Amsterdam Infection and Immunity Amsterdam University Medical Centers Amsterdam The Netherlands.

Frederic Geissmann (F)

Immunology Program Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center New York NY USA.

David Dombrowicz (D)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Bart Staels (B)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

David Montaigne (D)

Université de Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1011-EGID Lille France.

Classifications MeSH