Anti-diabetic drugs and weight loss in patients with type 2 diabetes.

Acarbose (PubChem CID: 41774) Anti-diabetic drugs Body composition Canagliflozin (PubChem CID: 24812758) Dapagliflozin (PubChem CID: 9887712) Diabesity Empagliflozin (PubChem CID: 11949646) Ertugliflozin (PubChem CID: 44814423) Exenatide (PubChem CID: 45588096) Liraglutide (PubChem CID: 16134956) Metformin (PubChem CID: 4091) Semaglutide (PubChem CID: 56843331) Type 2 diabetes Weight loss

Journal

Pharmacological research
ISSN: 1096-1186
Titre abrégé: Pharmacol Res
Pays: Netherlands
ID NLM: 8907422

Informations de publication

Date de publication:
09 2021
Historique:
received: 01 06 2021
revised: 17 07 2021
accepted: 20 07 2021
pubmed: 25 7 2021
medline: 3 3 2022
entrez: 24 7 2021
Statut: ppublish

Résumé

Obesity is frequently a comorbidity of type 2 diabetes. Even modest weight loss can significantly improve glucose homeostasis and lessen cardiometabolic risk factors in patients with type 2 diabetes, but lifestyle-based weight loss strategies are not long-term effective. There is an increasing need to consider pharmacological approaches to assist weight loss in the so called diabesity syndrome. Aim of this review is to analyze the weight-loss effect of non-insulin glucose lowering drugs in patients with type 2 diabetes. A systematic analysis of the literature on the effect of non-insulin glucose lowering drugs on weight loss in patients with type 2 diabetes was performed. For each class of drugs, the following parameters were analyzed: kilograms lost on average, effect on body mass index and body composition. Our results suggested that anti-diabetic drugs can be stratified into 3 groups based on their efficacy in weight loss: metformin, acarbose, empagliflozin and exenatide resulted in a in a mild weight loss (less than 3.2% of initial weight); canagliflozin, ertugliflozin, dapagliflozin and dulaglutide induces a moderate weight loss (between 3.2% and 5%); liraglutide, semaglutide and tirzepatide resulted in a strong weight loss (greater than 5%). This study shows that new anti-diabetic drugs, particularly GLP1-RA and Tirzepatide, are the most effective in inducing weight loss in patients with type 2 diabetes. Interestingly, exenatide appears to be the only GLP1-RA that induces a mild weight loss.

Identifiants

pubmed: 34302978
pii: S1043-6618(21)00366-2
doi: 10.1016/j.phrs.2021.105782
pii:
doi:

Substances chimiques

Glucagon-Like Peptide-1 Receptor 0
Hypoglycemic Agents 0
Gastric Inhibitory Polypeptide 59392-49-3
Glucagon-Like Peptide 1 89750-14-1

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

105782

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Elisa Lazzaroni (E)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Moufida Ben Nasr (M)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università Degli Studi Milano, Milan, Italy; Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Cristian Loretelli (C)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università Degli Studi Milano, Milan, Italy.

Ida Pastore (I)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Laura Plebani (L)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Maria Elena Lunati (ME)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Luciana Vallone (L)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Andrea Mario Bolla (AM)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Antonio Rossi (A)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Laura Montefusco (L)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy.

Elio Ippolito (E)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università Degli Studi Milano, Milan, Italy.

Cesare Berra (C)

Department of Endocrinology, Nutrition and Metabolic Diseases, IRCCS Multimedica, Milan, Italy.

Francesca D'Addio (F)

International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università Degli Studi Milano, Milan, Italy.

Gian Vincenzo Zuccotti (GV)

Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, Dept. Biomedical and Clinical Sciences "L. Sacco", Università di Milano and Pediatric Department, Buzzi Children's Hospital, Milan, Italy.

Paolo Fiorina (P)

Division of Endocrinology, ASST Fatebenefratelli-Sacco, Milan, Italy; International Center for T1D, Pediatric Clinical Research Center Romeo ed Enrica Invernizzi, DIBIC, Università Degli Studi Milano, Milan, Italy; Nephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: paolo.fiorina@childrens.harvard.edu.

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Classifications MeSH