Microbially Produced Imidazole Propionate Is Associated With Heart Failure and Mortality.
heart failure
histidine
imidazole propionate
microbiota
Journal
JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241
Informations de publication
Date de publication:
07 2023
07 2023
Historique:
received:
07
12
2022
revised:
01
03
2023
accepted:
16
03
2023
medline:
7
7
2023
pubmed:
28
4
2023
entrez:
28
4
2023
Statut:
ppublish
Résumé
Over the past years, it has become clear that the microbial ecosystem in the gut has a profound capacity to interact with the host through the production of a wide range of bioactive metabolites. The microbially produced metabolite imidazole propionate (ImP) is clinically and mechanistically linked with insulin resistance and type 2 diabetes, but it is unclear how ImP is associated with heart failure. The authors aimed to explore whether ImP is associated with heart failure and mortality. ImP serum measurements in 2 large and independent clinical cohorts of patients (European [n = 1,985] and North American [n = 2,155]) with a range of severity of cardiovascular disease including heart failure. Univariate and multivariate Cox regression analyses were performed to delineate the impact of ImP on 5-year mortality in the North American cohort, independent of other covariates. ImP is independently associated with reduced ejection fraction and heart failure in both cohorts, even after adjusting for traditional risk factors. Elevated ImP was a significant independent predictor of 5-year mortality (for the highest quartile, adjusted HR: 1.85 [95% CI: 1.20-2.88]; P < 0.01). The gut microbial metabolite ImP is increased in individuals with heart failure and is a predictor of overall survival.
Sections du résumé
BACKGROUND
Over the past years, it has become clear that the microbial ecosystem in the gut has a profound capacity to interact with the host through the production of a wide range of bioactive metabolites. The microbially produced metabolite imidazole propionate (ImP) is clinically and mechanistically linked with insulin resistance and type 2 diabetes, but it is unclear how ImP is associated with heart failure.
OBJECTIVES
The authors aimed to explore whether ImP is associated with heart failure and mortality.
METHODS
ImP serum measurements in 2 large and independent clinical cohorts of patients (European [n = 1,985] and North American [n = 2,155]) with a range of severity of cardiovascular disease including heart failure. Univariate and multivariate Cox regression analyses were performed to delineate the impact of ImP on 5-year mortality in the North American cohort, independent of other covariates.
RESULTS
ImP is independently associated with reduced ejection fraction and heart failure in both cohorts, even after adjusting for traditional risk factors. Elevated ImP was a significant independent predictor of 5-year mortality (for the highest quartile, adjusted HR: 1.85 [95% CI: 1.20-2.88]; P < 0.01).
CONCLUSIONS
The gut microbial metabolite ImP is increased in individuals with heart failure and is a predictor of overall survival.
Identifiants
pubmed: 37115134
pii: S2213-1779(23)00138-5
doi: 10.1016/j.jchf.2023.03.008
pii:
doi:
Substances chimiques
5-imidazolepropionic acid
1074-59-5
Imidazoles
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
810-821Subventions
Organisme : NHLBI NIH HHS
ID : P01 HL147823
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL103866
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126827
Pays : United States
Investigateurs
Renato Alves
(R)
Chloe Amouyal
(C)
Ehm Astrid Andersson Galijatovic
(EA)
Fabrizio Andreelli
(F)
Olivier Barthelemy
(O)
Jean-Philippe Bastard
(JP)
Jean-Paul Batisse
(JP)
Magalie Berland
(M)
Randa Bittar
(R)
Matthias Blüher
(M)
Peer Bork
(P)
Olivier Bourron
(O)
Mickael Camus
(M)
Dominique Cassuto
(D)
Cecile Ciangura
(C)
Luis Pedro Coelho
(LP)
Jean-Philippe Collet
(JP)
Marc-Emmanuel Dumas
(ME)
S Dusko Ehrlich
(SD)
Line Engelbrechtsen
(L)
Leopold Fezeu
(L)
Sofia Forslund
(S)
Sebastien Fromentin
(S)
Pilar Galan
(P)
Philippe Giral
(P)
Jens Peter Gøtze
(JP)
Torben Hansen
(T)
Tue H Hansen
(TH)
Agnes Hartemann
(A)
Bolette Hartmann
(B)
Serge Hercberg
(S)
Bridget Holmes
(B)
Jens Juul Holst
(JJ)
Malene Hornbak
(M)
Lesley Hoyles
(L)
Jean-Sebastien Hulot
(JS)
Sophie Jaqueminet
(S)
Mathieu Kerneis
(M)
Jean Khemis
(J)
Ruby Kozlowski
(R)
Helle Krogh Pedersen
(HK)
Michael Kuhn
(M)
Louise Mannerås-Holm
(L)
Lajos Marko
(L)
Laura Martinez-Gili Robin Massey
(L)
Nicolas Maziers
(N)
Jonathan Medina-Stamminger
(J)
Lucas Moitinho-Silva
(L)
Gilles Montalescot
(G)
Sandrine Moutel
(S)
Ana Luisa Neves
(AL)
Michael Olanipekun
(M)
Jean-Michel Oppert
(JM)
Christine Poitou
(C)
Francoise Pousset
(F)
Laurence Pouzoulet
(L)
Christine Rouault
(C)
Johanne Silvain
(J)
Henrik Vestergaard
(H)
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Funding Support and Author Disclosures This study was supported by the Transatlantic Networks of Excellence Award from the Leducq Foundation (17CVD01), FP7-sponsored program MetaCardis (305312), JPI (A healthy diet for a healthy life; 2017-01996_3), Swedish Heart Lung Foundation (20210366), Swedish Research Council (2019-01599), AFA insurances (160337), Knut and Alice Wallenberg Foundation (2017.0026), the Novo Nordisk Foundation (NNF15OC0016798), grants from the Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement (ALFGBG-718101 and ALFGBG-934173), and Bengt Ihre fellowship program. This work was also supported in part by grants from the National Institutes of Health (NIH) and the Office of Dietary Supplements (P01-HL147823, R01-HL103866, R01HL126827). The European clinical study is sponsored by Assistance Publique Hopitaux de Paris. The Novo Nordisk Foundation Center for Basic Metabolic Research is an independent research institution at the University of Copenhagen, partially funded by an unrestricted donation from the Novo Nordisk Foundation. Drs Bäckhed and Molinaro are shareholders in Implexion pharma AB. Dr Bäckhed is Torsten Söderberg Professor in Medicine and Wallenberg Scholar; and has received research funds from Biogaia AB. Dr Clément is a consultant for Danone Research and LNC therapeutics for work unassociated with the present study; and has held a collaborative research contract with Danone Research in the context of MetaCardis project. Dr Hazen has been named as co-inventor on pending and issued patents held by the Cleveland Clinic relating to cardiovascular diagnostics and therapeutics; has been a paid consultant for Zehna Therapeutics; has received research funds from Zehna Therapeutics, Procter and Gamble, and Roche Diagnostics; and has been eligible to receive royalty payments for inventions or discoveries related to cardiovascular diagnostics or therapeutics from Zehna Therapeutics, Cleveland HeartLab, a fully owned subsidiary of Quest Diagnostics, and Procter and Gamble. Dr Tang is a consultant for Sequana Medical A.G., Cardiol Therapeutics Inc, and Genomics plc; and has received honorarium from Springer Nature for authorship and editorship and the American Board of Internal Medicine for examination writing committee participation, all unrelated to the subject and contents of this paper. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.