The Real-World Observational Prospective Study of Health Outcomes with Dulaglutide and Liraglutide in Type 2 Diabetes Patients (TROPHIES): Design and Baseline Characteristics.

Dulaglutide Glucagon-like peptide 1 receptor agonists Injectable therapy Liraglutide Observational study design Patient characteristics Type 2 diabetes

Journal

Diabetes therapy : research, treatment and education of diabetes and related disorders
ISSN: 1869-6953
Titre abrégé: Diabetes Ther
Pays: United States
ID NLM: 101539025

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 15 03 2021
accepted: 08 05 2021
pubmed: 8 6 2021
medline: 8 6 2021
entrez: 7 6 2021
Statut: ppublish

Résumé

The TROPHIES observational study enrolled patients with type 2 diabetes mellitus (T2DM) initiating their first injectable treatment with the glucagon-like peptide 1 receptor agonists (GLP-1 RAs) dulaglutide or liraglutide. This manuscript focuses on the study design, baseline characteristics of the enrolled population, and factors associated with GLP-1 RA choice. TROPHIES is a prospective, observational, 24-month study conducted in France, Germany, and Italy. Inclusion criteria include adult patients with T2DM, naïve to injectable antihyperglycemic treatments, initiating dulaglutide or liraglutide per routine clinical practice. The primary outcome is the duration of treatment on dulaglutide or liraglutide without a significant treatment change. The analysis included 2181 patients (dulaglutide, 1130; liraglutide, 1051) (cutoff date May 15, 2019). The population was 56% male with mean [standard deviation (SD)] patient characteristics at baseline as follows: age, 59.2 (11.0) years; body mass index (BMI), 33.9 (6.6) kg/m This study analysis at baseline provides an opportunity to evaluate between-country differences in baseline HbA1c, weight, macrovascular complications, and factors driving GLP-1 RA selection for patients with T2DM in daily practice. Dulaglutide and liraglutide are medications that can help people with type 2 diabetes mellitus (T2DM) to control their blood sugar levels. These medications may also reduce body weight and reduce the risk of major cardiovascular disease. Given these treatment effects, it is essential to know how they are used in everyday clinical practice. Therefore, a study is being performed in three countries (France, Germany, and Italy) in people with T2DM who had a first-ever injectable therapy for T2DM with dulaglutide or liraglutide. Here, we present the study design, the patient characteristics at the start of treatment, and the factors driving the choice of one or the other medication. We analyzed data from 2181 people with T2DM. On average, it was shown that they were middle-aged and obese. On average, these people were diagnosed with T2DM 8.5 years before the start of dulaglutide or liraglutide and had high blood sugar levels when these medications were started. The patient characteristics were slightly different between the three countries. Country-specific factors driving the choice of either medication were also identified.

Autres résumés

Type: plain-language-summary (eng)
Dulaglutide and liraglutide are medications that can help people with type 2 diabetes mellitus (T2DM) to control their blood sugar levels. These medications may also reduce body weight and reduce the risk of major cardiovascular disease. Given these treatment effects, it is essential to know how they are used in everyday clinical practice. Therefore, a study is being performed in three countries (France, Germany, and Italy) in people with T2DM who had a first-ever injectable therapy for T2DM with dulaglutide or liraglutide. Here, we present the study design, the patient characteristics at the start of treatment, and the factors driving the choice of one or the other medication. We analyzed data from 2181 people with T2DM. On average, it was shown that they were middle-aged and obese. On average, these people were diagnosed with T2DM 8.5 years before the start of dulaglutide or liraglutide and had high blood sugar levels when these medications were started. The patient characteristics were slightly different between the three countries. Country-specific factors driving the choice of either medication were also identified.

Identifiants

pubmed: 34097244
doi: 10.1007/s13300-021-01076-0
pii: 10.1007/s13300-021-01076-0
pmc: PMC8266969
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1929-1946

Subventions

Organisme : Eli Lilly and Company
ID : The study was funded by Eli Lilly and Company

Références

Diabetes Ther. 2019 Jun;10(3):1067-1088
pubmed: 31028689
Diabetes Ther. 2017 Feb;8(1):115-128
pubmed: 28070733
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
Diabetes Ther. 2018 Apr;9(2):789-801
pubmed: 29525885
Diabetes Technol Ther. 2015 Mar;17(3):210-4
pubmed: 25353705
Lancet. 2019 Jul 13;394(10193):121-130
pubmed: 31189511
PLoS One. 2016 Mar 28;11(3):e0152281
pubmed: 27019360
Circulation. 2017 Aug 29;136(9):849-870
pubmed: 28847797
Diabetes Care. 2017 Nov;40(11):1469-1478
pubmed: 28801475
Diabetes Metab. 2015 Feb;41(1):55-61
pubmed: 25544682
Diabetes Care. 2018 Dec;41(12):2669-2701
pubmed: 30291106
Diabetes Ther. 2020 Oct;11(10):2383-2399
pubmed: 32880876
Diabetes Ther. 2014 Dec;5(2):499-520
pubmed: 25366334
Diabet Med. 1990 Jun;7(5):445-51
pubmed: 2142043
Stud Health Technol Inform. 2015;216:569-73
pubmed: 26262115
Curr Med Res Opin. 2019 May;35(5):893-901
pubmed: 30328731
N Engl J Med. 2016 Nov 10;375(19):1834-1844
pubmed: 27633186
Diabetes Obes Metab. 2018 Feb;20 Suppl 1:47-58
pubmed: 29364585
N Engl J Med. 2016 Jul 28;375(4):311-22
pubmed: 27295427
Diabetes Obes Metab. 2018 Feb;20 Suppl 1:5-21
pubmed: 29364588
Qual Life Res. 2006 Apr;15(3):481-91
pubmed: 16547787
J Patient Rep Outcomes. 2018 Sep 12;2:43
pubmed: 30294713
Diabetes Care. 2020 Feb;43(2):487-493
pubmed: 31857443
JAMA. 1997 Mar 19;277(11):925-6
pubmed: 9062334

Auteurs

Luis-Emilio García-Pérez (LE)

Lilly, S.A., Avenida de La Industria, 30, 28108, Alcobendas, Spain. garcia_luis-emilio@lilly.com.

Kristina S Boye (KS)

Eli Lilly and Company, Indianapolis, IN, USA.

Myriam Rosilio (M)

Lilly France SAS, Neuilly Sur Seine, France.

Heike Jung (H)

Lilly Deutschland GmbH, Bad Homburg, Germany.

Elke Heitmann (E)

Lilly Deutschland GmbH, Bad Homburg, Germany.

Kirsi Norrbacka (K)

Eli Lilly Finland, Helsinki, Finland.

Marco Orsini Federici (MO)

Eli Lilly and Company Italia SpA, Florence, Italy.

Raffaella Gentilella (R)

Eli Lilly and Company Italia SpA, Florence, Italy.

Bruno Guerci (B)

Hôpital Brabois Adultes, CHRU de Nancy and University of Lorraine, Nancy, France.

Francesco Giorgino (F)

University of Bari Aldo Moro, Bari, Italy.

Ulrich Aigner (U)

Versdias GmbH, Sulzbach-Rosenberg, Germany.

Hélène Sapin (H)

Lilly France SAS, Neuilly Sur Seine, France.

Classifications MeSH