Glycaemic control in patients with type 2 diabetes initiating 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:
01 2020
Historique:
received: 28 02 2019
revised: 31 07 2019
accepted: 25 08 2019
pubmed: 31 8 2019
medline: 21 5 2021
entrez: 31 8 2019
Statut: ppublish

Résumé

To assess glycaemic control and factors associated with poor glycaemic control at initiation of second-line therapy in the DISCOVER programme. DISCOVER (NCT02322762 and NCT02226822) comprises two similar prospective observational studies of 15 992 people with type 2 diabetes (T2D) initiating second-line glucose-lowering therapy in 38 countries across six regions (Africa, Americas, South-East Asia, Eastern Mediterranean, Europe and Western Pacific). Data were collected using a standardized case report form. Glycated haemoglobin (HbA1c) levels were measured according to standard clinical practice in each country, and factors associated with poor glycaemic control (HbA1c >8.0%) were evaluated using hierarchical regression models. HbA1c levels were available for 80.9% of patients (across-region range [ARR] 57.5%-97.5%); 92.2% (ARR 59.2%-99.1%) of patients had either HbA1c or fasting plasma glucose levels available. The mean HbA1c was 8.3% (ARR 7.9%-8.7%). In total, 26.7% of patients had an HbA1c level ≥9.0%, with the highest proportions in South-East Asia (35.6%). Factors associated with having HbA1c >8.0% at initiation of second-line therapy included low education level, low country income, and longer time since T2D diagnosis. The poor levels of glycaemic control at initiation of second-line therapy suggest that intensification of glucose-lowering treatment is delayed in many patients with T2D. In some countries, HbA1c levels are not routinely measured. These findings highlight an urgent need for interventions to improve monitoring and management of glycaemic control worldwide, particularly in lower-middle- and upper-middle-income countries.

Identifiants

pubmed: 31468637
doi: 10.1111/dom.13866
pmc: PMC6916552
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0

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

66-78

Subventions

Organisme : AstraZeneca
Pays : International

Informations de copyright

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

Références

Diabetes Metab Syndr Obes. 2018 Jan 31;11:15-21
pubmed: 29430192
Drugs. 2017 Mar;77(3):247-264
pubmed: 28155046
Rev Diabet Stud. 2006 Summer;3(2):82-7
pubmed: 17487331
Diabetes Care. 2013 Nov;36(11):3411-7
pubmed: 23877982
Ann Intern Med. 2012 Feb 7;156(3):218-31
pubmed: 22312141
Int J Gen Med. 2015 Feb 25;8:87-92
pubmed: 25759596
Diabetologia. 2015 Mar;58(3):429-42
pubmed: 25583541
Cardiovasc Diabetol. 2018 Nov 28;17(1):150
pubmed: 30486889
N Engl J Med. 2008 Oct 9;359(15):1577-89
pubmed: 18784090
Diabetes Care. 2017 Apr;40(4):468-475
pubmed: 27659408
Prim Care Diabetes. 2017 Apr;11(2):105-106
pubmed: 28222959
Diabetes Care. 2018 Dec;41(12):2669-2701
pubmed: 30291106
Diabetes Ther. 2018 Feb;9(1):165-175
pubmed: 29260460
Lancet Diabetes Endocrinol. 2018 Oct;6(10):798-808
pubmed: 30170949
Arch Intern Med. 2003 Jan 13;163(1):69-75
pubmed: 12523919
Diabetes Res Clin Pract. 2010 May;88 Suppl 1:S11-6
pubmed: 20466163
Clin Endocrinol (Oxf). 2014 Jan;80(1):47-56
pubmed: 23194193
J Clin Hypertens (Greenwich). 2010 Oct;12(10):826-32
pubmed: 21029348
J Endocrinol Invest. 2016 May;39(5):523-8
pubmed: 26385729
Cardiovasc Diabetol. 2015 Aug 07;14:100
pubmed: 26249018
Popul Health Manag. 2014 Aug;17(4):218-23
pubmed: 25127205
J Diabetes Complications. 2017 Jul;31(7):1188-1196
pubmed: 28499961
Diabetes Care. 2009 Feb;32(2):227-33
pubmed: 19033410
Diabetes Obes Metab. 2018 Feb;20(2):427-437
pubmed: 28834075
J Diabetes Metab Disord. 2014 Mar 04;13(1):40
pubmed: 24593933
Diabetes Care. 2013 Aug;36(8):2271-9
pubmed: 23418368
Int J Health Policy Manag. 2014 Dec 23;4(5):271-7
pubmed: 25905475
Diabetes Obes Metab. 2020 Jan;22(1):66-78
pubmed: 31468637
BMJ. 2000 Aug 12;321(7258):405-12
pubmed: 10938048
Endocr Pract. 2015 Apr;21(4):438-47
pubmed: 25877012
Diabetes Obes Metab. 2015 Mar;17(3):268-75
pubmed: 25425451
Int J Clin Pract. 2008 Nov;62(11):1809-19
pubmed: 18811598
N Engl J Med. 2008 Jun 12;358(24):2560-72
pubmed: 18539916

Auteurs

Kamlesh Khunti (K)

University of Leicester, Leicester, UK.

Hungta Chen (H)

AstraZeneca, Gaithersburg, Maryland.

Javier Cid-Ruzafa (J)

Evidera, Barcelona, Spain.

Peter Fenici (P)

AstraZeneca, Cambridge, UK.

Marilia B Gomes (MB)

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

Niklas Hammar (N)

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

Linong Ji (L)

Peking University People's Hospital, Beijing, People's Republic of China.

Mikhail Kosiborod (M)

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

Stuart Pocock (S)

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

Marina V Shestakova (MV)

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

Iichiro Shimomura (I)

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

Fengming Tang (F)

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

Hirotaka Watada (H)

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

Antonio Nicolucci (A)

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

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