How representative of a general type 2 diabetes population are patients included in cardiovascular outcome trials with SGLT2 inhibitors? A large European observational study.
SGLT2 inhibitors
cardiovascular disease
cardiovascular outcome trial
observational study
representativeness
Journal
Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
23
10
2018
revised:
01
12
2018
accepted:
05
12
2018
pubmed:
12
12
2018
medline:
8
9
2020
entrez:
12
12
2018
Statut:
ppublish
Résumé
Enrollment criteria vary substantially among cardiovascular outcome trials (CVOTs) of sodium-glucose cotransporter-2 inhibitors (SGLT-2is), which impacts the relationship between a trial population and the general type 2 diabetes (T2D) population. The aim of this study was to evaluate the representativeness of four SGLT-2i CVOTs of a general T2D population. T2D patients from Germany, The Netherlands, Norway and Sweden were included in the study. Given the available data per country, key inclusion and exclusion criteria were defined by diagnoses, procedures and drug treatments to facilitate comparability among countries. Representativeness was determined by dividing the number of patients fulfilling the key enrolment criteria of each CVOT (CANVAS, DECLARE-TIMI 58, EMPA-REG OUTCOME, VERTIS-CV) by the total T2D population. In 2015, a total T2D population of 803 836 patients was identified in Germany (n = 239 485), in The Netherlands (n = 36 213), in Norway (n = 149 782) and in Sweden (n = 378 356). These populations showed a 25% to 44% cardiovascular (CV) disease baseline prevalence and high CV-preventive drug use (>80%). The general T2D population had less prevalent CV disease and patients were slightly older than those included in the CVOTs. The DECLARE-TIMI 58 trial had the highest representativeness, 59% compared to the general T2D population, and this representativeness was almost 2-, 3- and 4-fold higher compared to the CANVAS (34%), EMPA-REG OUTCOME (21%) and VERTIS-CV (17%) trials, respectively. In large T2D populations within Europe, consistent patterns of representativeness of CVOTs were found when applying the main enrolment criteria. The DECLARE-TMI 58 trial had the highest representativeness, indicating that it included and examined patients who are most representative of the general T2D patients in the studied countries.
Identifiants
pubmed: 30537226
doi: 10.1111/dom.13612
pmc: PMC6590461
doi:
Substances chimiques
Sodium-Glucose Transporter 2 Inhibitors
0
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
968-974Informations de copyright
© 2018 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.
Références
Lancet. 2019 Jan 5;393(10166):31-39
pubmed: 30424892
N Engl J Med. 2019 Jan 24;380(4):347-357
pubmed: 30415602
J Am Med Inform Assoc. 2018 Mar 1;25(3):239-247
pubmed: 29025047
Circulation. 2017 Jul 18;136(3):249-259
pubmed: 28522450
Eur J Heart Fail. 2005 Aug;7(5):787-91
pubmed: 15916919
Lancet Diabetes Endocrinol. 2017 Sep;5(9):709-717
pubmed: 28781064
Clin J Am Soc Nephrol. 2017 May 8;12(5):751-759
pubmed: 28302903
Diabet Med. 2013 Mar;30(3):300-8
pubmed: 23075287
Eur J Cancer. 2010 Jan;46(2):395-404
pubmed: 19811904
Diabetes Obes Metab. 2019 Apr;21(4):968-974
pubmed: 30537226
Diabetes Obes Metab. 2018 Feb;20(2):344-351
pubmed: 28771923
Tidsskr Nor Laegeforen. 2015 Oct 20;135(19):1738-44
pubmed: 26486668
Am J Manag Care. 2018 Apr;24(8 Suppl):S138-S145
pubmed: 29693360
Eur J Heart Fail. 2008 Jul;10(7):658-60
pubmed: 18539522
J Am Coll Cardiol. 2018 Jun 12;71(23):2628-2639
pubmed: 29540325
N Engl J Med. 2017 Aug 17;377(7):644-657
pubmed: 28605608
Am Heart J. 2018 Jun;200:83-89
pubmed: 29898853
Am Heart J. 2018 Dec;206:11-23
pubmed: 30290289
N Engl J Med. 2015 Nov 26;373(22):2117-28
pubmed: 26378978
Diabetologia. 2016 Aug;59(8):1692-701
pubmed: 27189067
Diabetologia. 2018 Dec;61(12):2461-2498
pubmed: 30288571
BMC Public Health. 2011 Jun 09;11:450
pubmed: 21658213
BMJ Open. 2016 Nov 18;6(11):e012832
pubmed: 27864249