Gut Microbiome-Based Management of Patients With Heart Failure: JACC Review Topic of the Week.

cardiomyopathy gut microbiome heart failure personalized medicine precision medicine

Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
02 05 2023
Historique:
received: 07 10 2022
revised: 22 02 2023
accepted: 23 02 2023
medline: 28 4 2023
pubmed: 27 4 2023
entrez: 26 4 2023
Statut: ppublish

Résumé

Despite therapeutic advances, chronic heart failure (HF) is still associated with significant risk of morbidity and mortality. The course of disease and responses to therapies vary widely among individuals with HF, highlighting the need for precision medicine approaches. Gut microbiome stands to be an important aspect of precision medicine in HF. Exploratory clinical studies have revealed shared patterns of gut microbiome dysregulation in this disease, with mechanistic animal studies providing evidence for active involvement of the gut microbiome in development and pathophysiology of HF. Deeper insights into gut microbiome-host interactions in patients with HF promise to deliver novel disease biomarkers, preventative and therapeutic targets, and improve disease risk stratification. This knowledge may enable a paradigm shift in how we care for patients with HF, and pave the path toward improved clinical outcomes through personalized HF care.

Identifiants

pubmed: 37100490
pii: S0735-1097(23)04623-5
doi: 10.1016/j.jacc.2023.02.045
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1729-1739

Informations de copyright

Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Snyder is a co-founder and member of the scientific advisory boards of Personalis, SensOmics, Filtricine, Qbio, January, Mirvie, and Oralome; and is on the scientific advisory boards of Danaher, Genapsys, and Jupiter. Dr Tang has been supported by NIH 1R01HL126827; has served as a consultant for Sequana Medical, Cardiol Therapeutics, Genomics plc, Zehna Therapeutics, Renovacor, WhiteSwell, Kiniksa, Boston Scientific, and CardiaTec Biosciences; and has received honoraria from Springer Nature and American Board of Internal Medicine. Dr Mamic has reported that he has no relationships relevant to the contents of this paper to disclose.

Auteurs

Petra Mamic (P)

Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford University, Stanford, California, USA; Department of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, USA. Electronic address: mamic@stanford.edu.

Michael Snyder (M)

Department of Genetics, Stanford University School of Medicine, Stanford University, Stanford, California, USA.

W H Wilson Tang (WHW)

Kaufman Center for Heart Failure Treatment and Recovery, Heart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, Ohio, USA.

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Classifications MeSH