The effect of dapagliflozin on glycaemic control and other cardiovascular disease risk factors in type 2 diabetes mellitus: a real-world observational study.


Journal

Diabetologia
ISSN: 1432-0428
Titre abrégé: Diabetologia
Pays: Germany
ID NLM: 0006777

Informations de publication

Date de publication:
04 2019
Historique:
received: 21 05 2018
accepted: 30 11 2018
pubmed: 12 1 2019
medline: 19 2 2020
entrez: 12 1 2019
Statut: ppublish

Résumé

Dapagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, is indicated for improving glycaemic control in type 2 diabetes mellitus. Whether its effects on HbA We used data from the comprehensive national diabetes register, the Scottish Care Information-Diabetes (SCI-Diabetes) collaboration database, available from 2004 to mid-2016. Data within this database were linked to mortality data from the General Registrar, available from the Information Services Division (ISD) of the National Health Service in Scotland. We calculated crude within-person differences between pre- and post-drug-initiation values of HbA Among 8566 people exposed to dapagliflozin over a median of 210 days the crude within-person change in HbA Dapagliflozin exposure was associated with reductions in HbA

Identifiants

pubmed: 30631892
doi: 10.1007/s00125-018-4806-9
pii: 10.1007/s00125-018-4806-9
doi:

Substances chimiques

Benzhydryl Compounds 0
Blood Glucose 0
Glucosides 0
Sodium-Glucose Transporter 2 Inhibitors 0
dapagliflozin 1ULL0QJ8UC

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

621-632

Références

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Auteurs

Stuart J McGurnaghan (SJ)

MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.

Liam Brierley (L)

MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.

Thomas M Caparrotta (TM)

MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.

Paul M McKeigue (PM)

Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.

Luke A K Blackbourn (LAK)

MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.

Sarah H Wild (SH)

Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.

Graham P Leese (GP)

Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.

Rory J McCrimmon (RJ)

Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.

John A McKnight (JA)

Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.

Ewan R Pearson (ER)

Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.

John R Petrie (JR)

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, G12 8TA, UK.

Naveed Sattar (N)

Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, G12 8TA, UK.

Helen M Colhoun (HM)

MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK. helen.colhoun@igmm.ed.ac.uk.

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Classifications MeSH