All-cause mortality in patients with diabetes under glucagon-like peptide-1 agonists : a population-based, open cohort study

[thumbnail of WRAP-gestational-dyslipidaemia-adverse-birth-weight-Saravanan-2017.pdf] PDF
WRAP-gestational-dyslipidaemia-adverse-birth-weight-Saravanan-2017.pdf - Accepted Version
Embargoed item. Restricted access to Repository staff only - Requires a PDF viewer.
Available under License Creative Commons Attribution Non-commercial No Derivatives 4.0.

Download (709kB)

Request Changes to record.

Abstract

The glucagon-like peptide-1 receptor agonist (GLP1a) liraglutide has been described to benefit patients with type 2 diabetes mellitus (T2DM) at high cardiovascular risk. However, there are still uncertainties relating to these cardiovascular benefits: whether they also apply to an unselected diabetic population that includes low-risk patients, represent a class-effect, and could be observed in a real-world setting. We conducted a population-based, retrospective open cohort study using data derived from The Health Improvement Network database between Jan 2008 to Sept 2015. Patients with T2DM exposed to GLP1a (n=8345) were compared to age, gender, body mass index, duration of T2DM and smoking status-matched patients with T2DM unexposed to GLP1a (n=16,541). Patients with diabetes receiving GLP1a were significantly less likely to die from any cause compared to matched control patients with diabetes (adjusted incidence rate ratio [aIRR]: 0.64, 95% CI: 0.56-0.74, P-value<0.0001). Similar findings were observed in low-risk patients (aIRR: 0.64, 95% CI: 0.53-0.76, P -value=0.0001). No significant difference in the risk of incident CVD was detected in the low-risk patients (aIRR: 0.93, 95% CI: 0.83-1.12). Subgroup analyses suggested that effect is persistent in the elderly or across glycated haemoglobin categories. GLP1a treatment in a real-world setting may confer additional mortality benefit in patients with T2DM irrespective of their baseline CVD risk, age or baseline glycated haemoglobin and was sustained over the observation period.

Item Type: Journal Article
Subjects: R Medicine > RC Internal medicine
Divisions: Faculty of Science, Engineering and Medicine > Medicine > Warwick Medical School > Health Sciences > Population, Evidence & Technologies (PET)
Faculty of Science, Engineering and Medicine > Medicine > Warwick Medical School
SWORD Depositor: Library Publications Router
Library of Congress Subject Headings (LCSH): Non-insulin-dependent diabetes -- Treatment -- Risk factors, Cardiovascular system -- Diseases
Journal or Publication Title: Diabetes & Metabolism
Publisher: Elsevier Masson
ISSN: 1878-1780
Official Date: June 2017
Dates:
Date
Event
June 2017
Published
18 March 2017
Available
7 February 2017
Accepted
Volume: 43
Number: 3
Page Range: pp. 211-216
DOI: 10.1016/j.diabet.2017.02.003
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Restricted or Subscription Access
Date of first compliant deposit: 5 June 2018
RIOXX Funder/Project Grant:
Project/Grant ID
RIOXX Funder Name
Funder ID
UNSPECIFIED
University Of Birmingham
UNSPECIFIED
China Scholarship Council
81673181
[NSFC] National Natural Science Foundation of China
81703244
[NSFC] National Natural Science Foundation of China
2014A020213022
Guangdong Science and Technology Department
201508030037
Guangzhou Science and Technology Bureau
UNSPECIFIED
URI: https://wrap.warwick.ac.uk/87396/

Export / Share Citation


Request changes or add full text files to a record

Repository staff actions (login required)

View Item View Item