Glucagon-like Peptide-1 Receptor Analogues for the Treatment of Obesity.
Glucagon-like peptide-1 (GLP-1) receptor analogue
diabetes mellitus
liraglutide
obesity
overweight
semaglutide
type 2 diabetes
weight loss
weight management
Journal
TouchREVIEWS in endocrinology
ISSN: 2752-5457
Titre abrégé: touchREV Endocrinol
Pays: England
ID NLM: 101779126
Informations de publication
Date de publication:
Mar 2022
Mar 2022
Historique:
received:
26
08
2021
accepted:
05
01
2022
entrez:
17
8
2022
pubmed:
18
8
2022
medline:
18
8
2022
Statut:
ppublish
Résumé
There is an increasing prevalence of obesity worldwide, associated with significant morbidity and mortality, which frequently reduces quality of life and life expectancy. Consequently, there is a substantial and growing personal and economic burden necessitating the development of more effective therapies for obesity. Glucagon-like peptide-1 receptor analogues (GLP-1RAs) are licensed for the treatment of type 2 diabetes (T2D), and there is substantial evidence that these drugs not only improve cardiovascular outcomes but also promote weight loss. More recent evidence supports the use of the GLP-1RAs liraglutide and semaglutide in people with obesity without T2D. This article discusses the results of the major cardiovascular outcome trials for GLP-1RAs in people with T2D, the SCALE Obesity and Prediabetes study (Effect of liraglutide on body weight in non-diabetic obese subjects or overweight subjects with co-morbidities: SCALE™ - Obesity and Pre-diabetes; ClinicalTrials.gov identifier: NCT01272219; investigating liraglutide) and the STEP studies (Semaglutide treatment effect in people with obesity; assorted studies; investigating subcutaneous semaglutide). We also highlight the importance of a cost-effective approach to obesity pharmacotherapy. Clinicians should consider the use of GLP-1RAs in people with obesity, especially those with T2D or other obesity-related diseases, such as hypertension and dyslipidaemia. Ongoing trials, as well as clinical and cost-effectiveness appraisals, are anticipated over the next 12 months, and their findings may change the current landscape of obesity pharmacotherapy.
Identifiants
pubmed: 35975210
doi: 10.17925/EE.2022.18.1.43
pmc: PMC9354511
doi:
Banques de données
ClinicalTrials.gov
['NCT01272219']
Types de publication
Journal Article
Review
Langues
eng
Pagination
43-48Informations de copyright
© Touch Medical Media 2022.
Déclaration de conflit d'intérêts
Disclosures: David M Williams and Matthew Staff have no financial or non-financial relationships or activities to declare in relation to this article. Stephen C Bain reports grants and personal fees from AstraZeneca, Novo Nordisk and Sanofi-Aventis; personal fees from Boehringer Ingelheim, Eli Lilly and Merck Sharp & Dohme; grants from Medscape; expert advice provided to All-Wales Medicines Strategy Group and National Institute for Health and Care Excellence UK; and partnership in Glycosmedia. Thinzar Min reports personal fees and travel grants from AstraZeneca, Boehringer Ingelheim and Napp.
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