Glucagon-like peptide-1 receptor agonists improve outcomes in individuals with type 2 diabetes with and without heart failure.

Glucagon-like peptide-1 receptor agonists Heart failure Prognosis Type 2 diabetes mellitus

Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
09 Oct 2024
Historique:
received: 20 07 2024
revised: 12 09 2024
accepted: 30 09 2024
medline: 12 10 2024
pubmed: 12 10 2024
entrez: 11 10 2024
Statut: aheadofprint

Résumé

The effectiveness of glucagon-like peptide-1 receptor agonists (GLP1Ras) for prevention of heart failure (HF) in patients with type 2 diabetes (T2DM) without HF and for risk of death in patients with T2DM with HF has not been fully elucidated in routine clinical practice. Using the real-world global electronic medical record TriNetX database, individuals with T2DM and with or without HF who initiated either GLP1Ras or sitagliptin from 2017 to 2020 were retrospectively analyzed. In individuals with T2DM without HF, the primary outcome was a composite of all-cause mortality and a new diagnosis of HF within three years. In individuals with T2DM with HF, the primary outcome was all-cause mortality within three years. Propensity-score (PS) matching was used to adjust for over 100 baseline characteristics. A total of 65,598 individuals with T2DM without HF starting a GLP1Ras were PS matched with 65,598 starting sitagliptin. GLP1Ras were associated with a lower incidence of the composite endpoint (10.5 % versus 11.8 %, hazard ratio [HR] 0.82, [0.80-0.85], p < 0.001), mortality (HR 0.66 [0.63-0.69]) and new diagnosis of HF (HR 0.92 [0.88-0.96]). There were 6002 individuals in each group matched for T2DM and HF. Mortality was lower in the GLP1Ras group (17.6 % versus 22.8 %, HR 0.70 [0.65-0.76], p < 0.001). Results were consistent across subgroups. In this global real-world data analysis, GLP1Ra use was associated with a lower risk of death and HF in individuals with T2DM without HF, and lower risk of death in those with HF.

Sections du résumé

BACKGROUND BACKGROUND
The effectiveness of glucagon-like peptide-1 receptor agonists (GLP1Ras) for prevention of heart failure (HF) in patients with type 2 diabetes (T2DM) without HF and for risk of death in patients with T2DM with HF has not been fully elucidated in routine clinical practice.
METHODS METHODS
Using the real-world global electronic medical record TriNetX database, individuals with T2DM and with or without HF who initiated either GLP1Ras or sitagliptin from 2017 to 2020 were retrospectively analyzed. In individuals with T2DM without HF, the primary outcome was a composite of all-cause mortality and a new diagnosis of HF within three years. In individuals with T2DM with HF, the primary outcome was all-cause mortality within three years. Propensity-score (PS) matching was used to adjust for over 100 baseline characteristics.
RESULTS RESULTS
A total of 65,598 individuals with T2DM without HF starting a GLP1Ras were PS matched with 65,598 starting sitagliptin. GLP1Ras were associated with a lower incidence of the composite endpoint (10.5 % versus 11.8 %, hazard ratio [HR] 0.82, [0.80-0.85], p < 0.001), mortality (HR 0.66 [0.63-0.69]) and new diagnosis of HF (HR 0.92 [0.88-0.96]). There were 6002 individuals in each group matched for T2DM and HF. Mortality was lower in the GLP1Ras group (17.6 % versus 22.8 %, HR 0.70 [0.65-0.76], p < 0.001). Results were consistent across subgroups.
CONCLUSIONS CONCLUSIONS
In this global real-world data analysis, GLP1Ra use was associated with a lower risk of death and HF in individuals with T2DM without HF, and lower risk of death in those with HF.

Identifiants

pubmed: 39393444
pii: S0167-5273(24)01233-6
doi: 10.1016/j.ijcard.2024.132611
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

132611

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Yu Horiuchi received honoraria from TriNetX, Nippon Boehringer Ingelheim, Ono Pharmaceutical Company, AstraZeneca, Kyowa Kirin, Sanofi and Eli Lilly Japan. Nicholas Wettersten received grants from Department of Veterans Affairs National Institutes of Health, consulting fees from Guidepoint and honoraria from San Diego Heart Failure Symposium. Masahiko Asami received honoraria from Astellas, Daiichi Sankyo, AstraZeneca and Kyowa Kirin. Kazuyuki Yahagi received honoraria from Daiichi Sankyo and Nippon Boehringer Ingelheim. Hitomi Yuzawa received honoraria from Daiichi Sankyo. Kota Komiyama received honoraria from Astellas, Daiichi Sankyo, Ono Pharmaceutical and Kowa. Jun Tanaka received honoraria from Eli Lilly Japan, Novo Nordisk and Daiichi Sankyo. Jiro Aoki received honoraria from Daiichi Sankyo, Ono Pharmaceutical and Kowa, and has stock of Eli Lilly and Novo Nordisk. Kengo Tanabe received honoraria from Eli Lilly Japan, Novo Nordisk, Daiichi Sankyo, Ono Pharmaceutical, Industry, AstraZeneca and Kowa.

Auteurs

Yu Horiuchi (Y)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan. Electronic address: yooouyou@gmail.com.

Nicholas Wettersten (N)

Division of Cardiovascular Medicine, San Diego Veterans Affairs Medical Center, San Diego, California, USA; Division of Cardiovascular Medicine, University of California, San Diego/La Jolla, California, USA.

Masahiko Asami (M)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Kazuyuki Yahagi (K)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Kota Komiyama (K)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Hitomi Yuzawa (H)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Jun Tanaka (J)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Jiro Aoki (J)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Kengo Tanabe (K)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Classifications MeSH