Semaglutide for cardiovascular event reduction in people with overweight or obesity: SELECT study baseline characteristics.


Journal

Obesity (Silver Spring, Md.)
ISSN: 1930-739X
Titre abrégé: Obesity (Silver Spring)
Pays: United States
ID NLM: 101264860

Informations de publication

Date de publication:
01 2023
Historique:
revised: 13 09 2022
received: 26 07 2022
accepted: 28 09 2022
pubmed: 12 12 2022
medline: 23 12 2022
entrez: 11 12 2022
Statut: ppublish

Résumé

This paper describes the baseline characteristics of the Semaglutide Effects on Heart Disease and Stroke in Patients with Overweight or Obesity (SELECT) study, one of the largest cardiovascular (CV) outcome studies in the field of obesity, which evaluates the effect of semaglutide versus placebo on major CV events. SELECT enrolled individuals with overweight or obesity without diabetes, with prior myocardial infarction, stroke, and/or peripheral artery disease. This study reports participants' baseline characteristics in the full study population and subgroups defined by baseline glycated hemoglobin (HbA The study enrolled 17,605 participants (72.5% male) with an average (SD) age of 61.6 (8.9) years and BMI of 33.34 (5.04) kg/m The enrolled population in SELECT includes participants across a broad range of relevant risk categories. This will allow the study to garner information about the CV benefits of semaglutide across these relevant clinical subgroups.

Identifiants

pubmed: 36502289
doi: 10.1002/oby.23621
pmc: PMC10107832
doi:

Substances chimiques

Hypoglycemic Agents 0
semaglutide 53AXN4NNHX

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

111-122

Informations de copyright

© 2022 The Authors. Obesity published by Wiley Periodicals LLC on behalf of The Obesity Society.

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Auteurs

Ildiko Lingvay (I)

Department of Internal Medicine/Endocrinology and Department of Population and Data Sciences, UT Southwestern Medical Center, Dallas, Texas, USA.

Kirstine Brown-Frandsen (K)

Novo Nordisk A/S, Søborg, Denmark.

Helen M Colhoun (HM)

Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.

John Deanfield (J)

Farr Institute of Health Informatics Research at London, London, UK and National Institute for Cardiovascular Outcomes Research, University College London, London, UK.

Scott S Emerson (SS)

Department of Biostatistics, University of Washington, Seattle, Washington, USA.

Sille Esbjerg (S)

Novo Nordisk A/S, Søborg, Denmark.

Søren Hardt-Lindberg (S)

Novo Nordisk A/S, Søborg, Denmark.

G Kees Hovingh (GK)

Novo Nordisk A/S, Søborg, Denmark.

Steven E Kahn (SE)

Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, VA Puget Sound Health Care System and University of Washington, Seattle, Washington, USA.

Robert F Kushner (RF)

Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.

A Michael Lincoff (AM)

Cleveland Clinic Coordinating Center for Clinical Research (C5Research) and Department of Cardiovascular Medicine, Cleveland, Ohio, USA.

Steven P Marso (SP)

HCA Midwest Health Heart and Vascular Institute, Kansas City, Missouri, USA.

Tea Monk Fries (TM)

Novo Nordisk A/S, Søborg, Denmark.

Jorge Plutzky (J)

Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Donna H Ryan (DH)

Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana, USA.

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Classifications MeSH