Semaglutide Effects on Cardiovascular Outcomes in People With Overweight or Obesity (SELECT) rationale and design.


Journal

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

Informations de publication

Date de publication:
11 2020
Historique:
received: 03 05 2020
accepted: 08 07 2020
pubmed: 12 9 2020
medline: 15 12 2020
entrez: 11 9 2020
Statut: ppublish

Résumé

Cardiovascular disease (CVD) is a major cause of morbidity and mortality. Although it has been widely appreciated that obesity is a major risk factor for CVD, treatments that produce effective, durable weight loss and the impact of weight reduction in reducing cardiovascular risk have been elusive. Instead, progress in CVD risk reduction has been achieved through medications indicated for controlling lipids, hyperglycemia, blood pressure, heart failure, inflammation, and/or thrombosis. Obesity has been implicated as promoting all these issues, suggesting that sustained, effective weight loss may have independent cardiovascular benefit. GLP-1 receptor agonists (RAs) reduce weight, improve glycemia, decrease cardiovascular events in those with diabetes, and may have additional cardioprotective effects. The GLP-1 RA semaglutide is in phase 3 studies as a medication for obesity treatment at a dose of 2.4 mg subcutaneously (s.c.) once weekly. Semaglutide Effects on Heart Disease and Stroke in Patients with Overweight or Obesity (SELECT) is a randomized, double-blind, parallel-group trial testing if semaglutide 2.4 mg subcutaneously once weekly is superior to placebo when added to standard of care for preventing major adverse cardiovascular events in patients with established CVD and overweight or obesity but without diabetes. SELECT is the first cardiovascular outcomes trial to evaluate superiority in major adverse cardiovascular events reduction for an antiobesity medication in such a population. As such, SELECT has the potential for advancing new approaches to CVD risk reduction while targeting obesity.

Identifiants

pubmed: 32916609
pii: S0002-8703(20)30214-3
doi: 10.1016/j.ahj.2020.07.008
pii:
doi:

Substances chimiques

Cardiotonic Agents 0
Hypoglycemic Agents 0
semaglutide 53AXN4NNHX
Glucagon-Like Peptides 62340-29-8
Glucagon-Like Peptide 1 89750-14-1

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

61-69

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Donna H Ryan (DH)

Pennington Biomedical Research Center, Baton Rouge, LA.

Ildiko Lingvay (I)

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

Helen M Colhoun (HM)

Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.

John Deanfield (J)

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

Scott S Emerson (SS)

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

Steven E Kahn (SE)

VA Puget Sound Health Care System and University of Washington, Seattle, WA.

Robert F Kushner (RF)

Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.

Steve Marso (S)

HCA Midwest Health Heart and Vascular Institute, Kansas City, MO.

Jorge Plutzky (J)

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

Kirstine Brown-Frandsen (K)

Novo Nordisk A/S, Søborg, Denmark.

Marianne O L Gronning (MOL)

Novo Nordisk A/S, Søborg, Denmark.

G Kees Hovingh (GK)

Novo Nordisk A/S, Søborg, Denmark; Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands.

Anders Gaarsdal Holst (AG)

Novo Nordisk A/S, Søborg, Denmark.

Henrik Ravn (H)

Novo Nordisk A/S, Søborg, Denmark.

A Michael Lincoff (AM)

Department of Cardiovascular Medicine, Cleveland Clinic Coordinating Center for Clinical Research (C5Research), Cleveland, OH. Electronic address: lincofa@ccf.org.

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Classifications MeSH