All-cause mortality in patients with diabetes under treatment with dapagliflozin: a population-based, open-cohort study in THIN database

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Abstract

Context: Empagliflozin was found to decrease mortality in patients with type 2 diabetes (T2DM) and a prior cardiovascular (CVD) event.

Objectives: To establish whether these benefits can be replicated in a real-world setting, should be expected with the use of dapagliflozin, and apply to T2DM patients at low risk of CVD.

Design: General Practice, population-based, retrospective cohort study (January 2013-September 2015).

Setting: The Health Improvement Network Database (THIN).

Participants: A total of 22,124 patients (4,444 exposed to dapagliflozin, 17,680 unexposed T2DM patients), matched for age, sex, body mass index, T2DM duration and smoking.

Main outcome measures: The primary outcome was all-cause mortality in the total study (high and low risk for CVD) population expressed as the adjusted incidence rate ratio (aIRR) with 95% confidence intervals (CI). As a secondary analysis in the low risk population, all-cause mortality and incident cardiovascular disease (CVD) were considered.

Results: Patients with T2DM exposed to dapagliflozin were significantly less likely to die from any cause (0.50, 95% CI: 0.33-0.75, p-value = 0.001). Similarly, in low risk patients, death from any cause was significantly lower in the exposed to dapagliflozin cohort (aIRR: 0.44, 95% CI: 0.25-0.78, p-value = 0.002). The difference in the risk of incident CVD did not reach statistical significance between groups in low-risk patients (aIRR: 0.89, 95% CI: 0.61-1.31, p-value = 0.546).

Conclusions: Patients with T2DM exposed to dapagliflozin were at a lower risk of death from any cause irrespective of baseline CVD status. In a population-based, open cohort study, patients with T2DM exposed to dapagliflozin were at a lower risk of death from any cause irrespective of their baseline CVD risk.
Original languageEnglish
Pages (from-to)1719-1725
Number of pages7
JournalJournal of Clinical Endocrinology and Metabolism
Volume102
Issue number5
Early online date20 Feb 2017
DOIs
Publication statusPublished - 1 May 2017

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