Treatment patterns and associated factors in 14 668 people with type 2 diabetes initiating a second-line therapy: Results from the global DISCOVER study programme.


Journal

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

Informations de publication

Date de publication:
11 2019
Historique:
received: 13 03 2019
revised: 28 06 2019
accepted: 04 07 2019
pubmed: 13 7 2019
medline: 29 9 2020
entrez: 13 7 2019
Statut: ppublish

Résumé

To evaluate treatment data from DISCOVER (NCT02322762 and NCT02226822), a global, prospective, observational study programme of patients with type 2 diabetes initiating a second-line glucose-lowering therapy. Data were collected using a standardized case report form. First- and second-line treatments were assessed in 14 668 patients from 37 countries across six regions. Among patients prescribed first-line metformin monotherapy, Firth logistic regression models were used to assess factors associated with second-line treatment choices. The most common first-line therapies were metformin monotherapy (57.9%) and combinations of metformin with a sulphonylurea (14.6%). The most common second-line therapies were combinations of metformin with other agents (72.2%), including dipeptidyl peptidase-4 (DPP-4) inhibitors (25.1%) or sulphonylureas (21.3%). Among patients prescribed first-line metformin monotherapy, the most common second-line therapies were combinations of metformin with a DPP-4 inhibitor [32.8%; across-region range (ARR): 2.4%-51.3%] or a sulphonylurea (30.0%; ARR: 18.3%-63.6%); only a few patients received combinations of metformin with sodium-glucose co-transporter-2 inhibitors (6.7%; ARR: 0.0%-10.8%) or glucagon-like peptide-1 receptor agonists (1.9%; ARR: 0.1%-4.5%). Both clinical and non-medical factors were associated with choice of second-line therapy after metformin monotherapy. Fewer patients than expected received metformin monotherapy at first line, and the use of newer therapies at second line was uncommon in some regions of the world. Patients' socioeconomic status was associated with treatment patterns, suggesting that therapy choices are influenced by cost and access.

Identifiants

pubmed: 31297947
doi: 10.1111/dom.13830
pmc: PMC6852520
doi:

Substances chimiques

Dipeptidyl-Peptidase IV Inhibitors 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin 0
hemoglobin A1c protein, human 0
Metformin 9100L32L2N

Banques de données

ClinicalTrials.gov
['NCT02322762', 'NCT02226822']

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2474-2485

Informations de copyright

© 2019 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Antonio Nicolucci (A)

Center for Outcomes Research and Clinical Epidemiology, Pescara, Italy.

Bernard Charbonnel (B)

University of Nantes, Nantes, France.

Marília B Gomes (MB)

Rio de Janeiro State University, Rio de Janeiro, Brazil.

Kamlesh Khunti (K)

University of Leicester, Leicester, UK.

Mikhail Kosiborod (M)

Saint Luke's Mid America Heart Institute, Kansas City, Missouri.
University of Missouri, Kansas City, Missouri.
The George Institute for Global Health, Sydney, Australia.

Marina V Shestakova (MV)

Endocrinology Research Center, Diabetes Institute, Moscow, Russian Federation.

Iichiro Shimomura (I)

Graduate School of Medicine, Osaka University, Osaka, Japan.

Hirotaka Watada (H)

Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Hungta Chen (H)

AstraZeneca, Gaithersburg, Maryland.

Javier Cid-Ruzafa (J)

Evidera, Barcelona, Spain.

Peter Fenici (P)

AstraZeneca, Cambridge, UK.

Niklas Hammar (N)

Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden.

Filip Surmont (F)

AstraZeneca, Luton, UK.

Fengming Tang (F)

Saint Luke's Mid America Heart Institute, Kansas City, Missouri.

Stuart Pocock (S)

London School of Hygiene and Tropical Medicine, London, UK.

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Classifications MeSH