Regional variation of effects of new antidiabetic medications in cardiovascular outcome trials.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
10 2021
Historique:
received: 07 01 2021
accepted: 02 06 2021
pubmed: 10 6 2021
medline: 25 2 2023
entrez: 9 6 2021
Statut: ppublish

Résumé

In international trials, glucagon-like protein-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter-2 inhibitors (SGLT2Is) were effective in improving cardiovascular (CV) outcomes. We assessed the effect of GLP-1RAs and SGLT2Is treatment effect on CV endpoints by geographical region in multiple international trials using random effects weighted least squares meta-regressions. The estimated effects of both SGLT2Is and GLP-1RAs on major adverse CV events (MACE) in North America (SGLT2Is n = 12,399, HR 0.90, 95% CI 0.81-1.01; GLP-1RAs n = 12,515, HR 0.95, 95% CI 0.83- 1.09) and in Europe (SGLT2Is n = 19,435, HR 0.93, 95% CI 0.85-1.02; GLP-1RAs n = 22,812, HR 0.88, 95% CI 0.79-0.99) were numerically lower but not statistically different to the rest of the world (ROW) (SGLT2Is n = 15,127, HR 0.83, 95% CI 0.75-0.92, p-value for interaction 0.26; GLP-1RAs n = 17,494, HR 0.82, 95% CI 0.73-0.92, p-value for interaction 0.28). Effects of SGLT2Is on heart failure readmission or CV death varied significantly by region (P = 0.0094). The effect of SGLT2Is was significantly smaller in Europe (n = 18,653, HR 0.86, 95% CI 0.78-0.95) than in the ROW (n = 12,463, HR 0.68, 95% CI 0.61-0.76, P = 0.0024). The smaller effect in North America (n = 9776, HR 0.76, 95% CI 0.66-0.87) did not differ significantly from that in the ROW (P = 0.2370). The effects of SGLT2Is on HF events are larger in the ROW. Further analyses and studies are needed to better elucidate the differential effects of SGLTIs and GLP-1RAs by geographical regions.

Sections du résumé

BACKGROUND
In international trials, glucagon-like protein-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter-2 inhibitors (SGLT2Is) were effective in improving cardiovascular (CV) outcomes.
METHODS
We assessed the effect of GLP-1RAs and SGLT2Is treatment effect on CV endpoints by geographical region in multiple international trials using random effects weighted least squares meta-regressions.
RESULTS
The estimated effects of both SGLT2Is and GLP-1RAs on major adverse CV events (MACE) in North America (SGLT2Is n = 12,399, HR 0.90, 95% CI 0.81-1.01; GLP-1RAs n = 12,515, HR 0.95, 95% CI 0.83- 1.09) and in Europe (SGLT2Is n = 19,435, HR 0.93, 95% CI 0.85-1.02; GLP-1RAs n = 22,812, HR 0.88, 95% CI 0.79-0.99) were numerically lower but not statistically different to the rest of the world (ROW) (SGLT2Is n = 15,127, HR 0.83, 95% CI 0.75-0.92, p-value for interaction 0.26; GLP-1RAs n = 17,494, HR 0.82, 95% CI 0.73-0.92, p-value for interaction 0.28). Effects of SGLT2Is on heart failure readmission or CV death varied significantly by region (P = 0.0094). The effect of SGLT2Is was significantly smaller in Europe (n = 18,653, HR 0.86, 95% CI 0.78-0.95) than in the ROW (n = 12,463, HR 0.68, 95% CI 0.61-0.76, P = 0.0024). The smaller effect in North America (n = 9776, HR 0.76, 95% CI 0.66-0.87) did not differ significantly from that in the ROW (P = 0.2370).
CONCLUSION
The effects of SGLT2Is on HF events are larger in the ROW. Further analyses and studies are needed to better elucidate the differential effects of SGLTIs and GLP-1RAs by geographical regions.

Identifiants

pubmed: 34107289
pii: S0002-8703(21)00148-4
doi: 10.1016/j.ahj.2021.06.001
pii:
doi:

Substances chimiques

Glucagon-Like Peptide-1 Receptor 0
Hypoglycemic Agents 0
Sodium-Glucose Transporter 2 Inhibitors 0

Types de publication

Journal Article Meta-Analysis

Langues

eng

Sous-ensembles de citation

IM

Pagination

73-80

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Gad Cotter (G)

Momentum Research Inc, Durham, North Carolina; Inserm U942 MASCOT, Paris, France. Electronic address: gadcotter@momentum-research.com.

Beth A Davison (BA)

Momentum Research Inc, Durham, North Carolina; Inserm U942 MASCOT, Paris, France.

Christopher Edwards (C)

Momentum Research Inc, Durham, North Carolina.

Stefanie Senger (S)

Momentum Research Inc, Durham, North Carolina.

John R Teerlink (JR)

Section of Cardiology, San Francisco Veterans Affairs Medical Center and School of Medicine, University of California San Francisco,San Francisco, CA.

Faiez Zannad (F)

Inserm CIC-P 1433, Université de Lorraine, CHRU de Nancy, FCRIN INI-CRCT, Nancy, France.

Olav Wendelboe Nielsen (OW)

Department of Cardiology, Bispebjerg Hospital, University of Copenhagen, Denmark.

Marco Metra (M)

Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Italy.

Alexandre Mebazaa (A)

Department of Anesthesiology and Critical Care Medicine, AP-HP, Saint Louis Lariboisière University Hospitals, Université de Paris, Paris, France.

Ovidiu Chioncel (O)

University of Medicine Carol Davila, Bucharest, Romania.

Barry H Greenberg (BH)

Division of Cardiology, University of California San Diego, California.

Aldo P Maggioni (AP)

Associazione Nazionale Medici Cardiologi Ospedalien (ANMCO) Research Center, Florence, Italy.

Georg Ertl (G)

Julius-Maximilians-Universität Würzburg, Germany.

Naoki Sato (N)

Cardiology and Intensive Care Unit, Nippon Medical School, Musashi-Kosugi Hospital, Kawasaki, Japan.

Alain Cohen-Solal (A)

Service de Cardiologie, Hôpital Lariboisière, 75010 Paris, France.

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Classifications MeSH