Treatment patterns and glycated haemoglobin levels over 36 months in individuals with type 2 diabetes initiating second-line glucose-lowering therapy: The global DISCOVER study.

antidiabetic drug glycaemic control observational study second-line treatment 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:
01 2023
Historique:
revised: 08 08 2022
received: 06 04 2022
accepted: 16 08 2022
pubmed: 17 9 2022
medline: 15 12 2022
entrez: 16 9 2022
Statut: ppublish

Résumé

To describe glucose-lowering treatment regimens and glycated haemoglobin (HbA1c) trajectories in individuals with type 2 diabetes (T2D) over 36 months of follow-up from the start of second-line therapy. This data analysis from the 3-year, observational DISCOVER study programme included 14 687 participants from 37 countries with T2D initiating second-line glucose-lowering therapy. Treatment and HbA1c data were collected at baseline (start of second-line therapy) and at 6, 12, 24 and 36 months. Treatment regimen changes over follow-up were analysed using the McNemar test, with carry-forward imputation for intermediate missing values. A total of 11 592 participants had treatment data at baseline and 36 months, and 11 882 had HbA1c data at baseline. At baseline and 36 months, respectively, rates of oral monotherapy use were 12.1% and 12.4% (P = 0.22), rates of dual oral therapy use were 63.4% and 47.6% (P < 0.0001), rates of ≥ triple oral therapy use were 17.5% and 25.4% (P < 0.0001), and rates of injectable treatment use were 7.0% and 13.7% (P < 0.0001). Use of injectable drugs was most common among participants with an HbA1c level ≥64 mmol/mol (≥8.0%). Overall, 42.9% of participants changed treatment during follow-up. Mean HbA1c levels at baseline and 6 months were 67 mmol/mol (8.3%) and 55 mmol/mol (7.2%), respectively, remaining stable thereafter. Dual oral therapy was the most common treatment regimen at the start of second-line treatment, and over half of the participants remained on the same treatment during follow-up.

Identifiants

pubmed: 36111434
doi: 10.1111/dom.14842
pmc: PMC10087302
doi:

Substances chimiques

Glycated Hemoglobin 0
Glucose IY9XDZ35W2

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

46-55

Informations de copyright

© 2022 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Bernard H Charbonnel (BH)

Department of Endocrinology and Diabetes, University of Nantes, Nantes, France.

Hungta Chen (H)

BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland, USA.

Javier Cid-Ruzafa (J)

Evidera, Barcelona, Spain.

Andrew Cooper (A)

BioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.

Peter Fenici (P)

BioPharmaceuticals Medical, AstraZeneca, Milan, Italy.

Marilia B Gomes (MB)

Department of Internal Medicine, Rio de Janeiro State University, Rio de Janeiro, Brazil.

Gabriela L Saraiva (GL)

BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland, USA.

Jesús Medina (J)

BioPharmaceuticals Medical, AstraZeneca, Madrid, Spain.

Antonio Nicolucci (A)

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

Marina V Shestakova (MV)

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

Iichiro Shimomura (I)

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

Filip Surmont (F)

BioPharmaceuticals Medical, AstraZeneca, Luton, UK.

Fengming Tang (F)

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

Jiten Vora (J)

Royal Liverpool University Hospital, Liverpool, UK.

Hirotaka Watada (H)

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

Kamlesh Khunti (K)

Diabetes Research Centre, University of Leicester, Leicester, UK.

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