Liraglutide hospital discharge trial: A randomized controlled trial comparing the safety and efficacy of liraglutide versus insulin glargine for the management of patients with type 2 diabetes after hospital discharge.


Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
06 2021
Historique:
revised: 21 01 2021
received: 20 11 2020
accepted: 23 01 2021
pubmed: 17 2 2021
medline: 10 7 2021
entrez: 16 2 2021
Statut: ppublish

Résumé

To compare a glucagon-like peptide-1 receptor agonist with basal insulin at hospital discharge in patients with uncontrolled type 2 diabetes in a randomized clinical trial. A total of 273 patients with glycated haemoglobin (HbA1c) 7%-10% (53-86 mol/mol) were randomized to liraglutide (n = 136) or insulin glargine (n = 137) at hospital discharge. The primary endpoint was difference in HbA1c at 12 and 26 weeks. Secondary endpoints included hypoglycaemia, changes in body weight, and achievement of HbA1c <7% (53 mmol/mol) without hypoglycaemia or weight gain. The between-group difference in HbA1c at 12 weeks and 26 weeks was -0.28% (95% CI -0.64, 0.09), and at 26 weeks it was -0.55%, (95% CI -1.01, -0.09) in favour of liraglutide. Liraglutide treatment resulted in a lower frequency of hypoglycaemia <3.9 mmol/L (13% vs 23%; P = 0.04), but there was no difference in the rate of clinically significant hypoglycaemia <3.0 mmol/L. Compared to insulin glargine, liraglutide treatment was associated with greater weight loss at 26 weeks (-4.7 ± 7.7 kg vs -0.6 ± 11.5 kg; P < 0.001), and the proportion of patients with HbA1c <7% (53 mmol/mol) without hypoglycaemia was 48% versus 33% (P = 0.05) at 12 weeks and 45% versus 33% (P = 0.14) at 26 weeks in liraglutide versus insulin glargine. The proportion of patients with HbA1c <7% (53 mmol/mol) without hypoglycaemia and no weight gain was higher with liraglutide at 12 (41% vs 24%, P = 0.005) and 26 weeks (39% vs 22%; P = 0.014). The incidence of gastrointestinal adverse events was higher with liraglutide than with insulin glargine (P < 0.001). Compared to insulin glargine, treatment with liraglutide at hospital discharge resulted in better glycaemic control and greater weight loss, but increased gastrointestinal adverse events.

Identifiants

pubmed: 33591621
doi: 10.1111/dom.14347
pmc: PMC8571803
mid: NIHMS1744534
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin Glargine 2ZM8CX04RZ
Liraglutide 839I73S42A

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1351-1360

Subventions

Organisme : NIGMS NIH HHS
ID : K23 GM128221
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK111024
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK113241
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK123384
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002378
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK122199
Pays : United States

Informations de copyright

© 2021 John Wiley & Sons Ltd.

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Auteurs

Francisco J Pasquel (FJ)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Maria A Urrutia (MA)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Saumeth Cardona (S)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Karla W Z Coronado (KWZ)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Bonnie Albury (B)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Mireya C Perez-Guzman (MC)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Rodolfo J Galindo (RJ)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Ajay Chaudhuri (A)

Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, New York.

Gianluca Iacobellis (G)

Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami, Miami, Florida.

Juan Palacios (J)

Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Miami, Miami, Florida.

Javier M Farias (JM)

Division of Endocrinology Sanatorio Guemes, Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina.

Patricia Gomez (P)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Isabel Anzola (I)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Priyathama Vellanki (P)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Maya Fayfman (M)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Georgia M Davis (GM)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Alexandra L Migdal (AL)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Limin Peng (L)

Deartment of Biostatistics, Rollins School of Public Health, Emory University, Atlanta, Georgia.

Guillermo E Umpierrez (GE)

Division of Endocrinology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

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Classifications MeSH