The Real-World Observational Prospective Study of Health Outcomes with Dulaglutide and Liraglutide in Patients with Type 2 Diabetes (TROPHIES): Patient disposition, clinical characteristics and treatment persistence at 12 months.
Humans
Liraglutide
Diabetes Mellitus, Type 2
/ drug therapy
Prospective Studies
Glycated Hemoglobin
Drug Administration Schedule
Glucagon-Like Peptides
Immunoglobulin Fc Fragments
/ adverse effects
Recombinant Fusion Proteins
/ adverse effects
Hypoglycemic Agents
Glucagon-Like Peptide 1
Outcome Assessment, Health Care
Glucagon-Like Peptide-1 Receptor
/ agonists
antidiabetic drug
dulaglutide
liraglutide
observational study
type 2 diabetes
Journal
Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645
Informations de publication
Date de publication:
12 2022
12 2022
Historique:
revised:
14
07
2022
received:
10
03
2022
accepted:
15
07
2022
pubmed:
26
7
2022
medline:
1
11
2022
entrez:
25
7
2022
Statut:
ppublish
Résumé
The primary objective of the TROPHIES observational study is to estimate the duration of treatment on dulaglutide or liraglutide without a significant treatment change by 24 months in patients with type 2 diabetes (T2D) initiating their first injectable treatment with these glucagon-like peptide-1 receptor agonists (GLP-1 RAs). This manuscript presents 12-month interim data. TROPHIES is a prospective, non-comparative, observational study of patients with T2D in Europe, naïve to injectable antihyperglycaemic treatments and initiating dulaglutide or liraglutide. Data on clinical characteristics, GLP-1 RA persistence and treatment patterns of glucose-lowering medication were collected at initiation of first injectable therapy and by 12 months. By 12 months, 1014 dulaglutide and 991 liraglutide patients were eligible across France, Germany and Italy. Both cohorts presented a high probability [95% confidence interval (CI)] of GLP-1 RA persistence [dulaglutide, 0.88 (0.86 to 0.90); liraglutide, 0.83 (0.80 to 0.85)] and reduction in mean glycated haemoglobin percentage (95% CI) from baseline [dulaglutide, -1.18 (-1.27 to -1.08); liraglutide, -1.15 (-1.26 to -1.05)] with 48.2% of dulaglutide and 41.2% of liraglutide patients reaching their individualized glycated haemoglobin percentage target set by the physician at baseline. Mean weight (95% CI) change from baseline was -3.2 kg (-3.6 to -2.8) for dulaglutide and -3.4 kg (-3.9 to -3.0) for liraglutide. Slight changes in concomitant medications were observed compared with baseline. In the real-world setting, dulaglutide and liraglutide cohorts achieved good persistence with similarly improved glycaemic control that was accompanied by weight loss at 12 months, consistent with previous clinical trial results.
Identifiants
pubmed: 35876235
doi: 10.1111/dom.14823
pmc: PMC9804517
doi:
Substances chimiques
dulaglutide
WTT295HSY5
Liraglutide
839I73S42A
Glycated Hemoglobin A
0
Glucagon-Like Peptides
62340-29-8
Immunoglobulin Fc Fragments
0
Recombinant Fusion Proteins
0
Hypoglycemic Agents
0
Glucagon-Like Peptide 1
89750-14-1
Glucagon-Like Peptide-1 Receptor
0
Types de publication
Observational Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2373-2382Informations de copyright
© 2022 Eli Lilly and Company and The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.
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