How representative of a general type 2 diabetes population are patients included in cardiovascular outcome trials with SGLT2 inhibitors? A large European observational study.


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
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

968-974

Informations de copyright

© 2018 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Kåre I Birkeland (KI)

Department of Transplantation Medicine, Division of Surgery, Inflammatory Medicine and Transplantation, Oslo University Hospital and University of Oslo, Oslo, Norway.

Johan Bodegard (J)

AstraZeneca Nordic-Baltic, Oslo, Norway.

Anna Norhammar (A)

Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.

Josephina G Kuiper (JG)

PHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.

Elena Georgiado (E)

Team Gesundheit GmbH, Essen, Germany.

Wendy L Beekman-Hendriks (WL)

AstraZeneca, Den Haag, The Netherlands.

Marcus Thuresson (M)

Statisticon AB, Uppsala, Sweden.

Marc Pignot (M)

Kantar Health GmbH, Munich, Germany.

Ron M C Herings (RMC)

PHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.
Department of Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, The Netherlands.

Adriaan Kooy (A)

University Medical Center Groningen and Bethesda Diabetes Research Center, Hoogeveen, Groningen, The Netherlands.

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