MedicalResearch.com Interview with:
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Prof. McMurray[/caption]
John J. V. McMurray, MD FRCP FESC FACC FAHA FRSE FMedSci
British Heart Foundation Cardiovascular Research Centre
University of Glasgow
Glasgow, United Kingdom
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Dr. Docherty[/caption]
Kieran F Docherty
DAPA-HF investigator
British Heart Foundation Cardiovascular Research Centre,
University of Glasgow
MedicalResearch.com: What is the background for this study?
Response: DAPA-HF was a double-blind randomized controlled trial comparing dapagliflozin 10 mg once daily with placebo in 4744 patients with heart failure and reduced ejection fraction (HFrEF).
The primary outcome was a composite of time to occurrence of a worsening heart failure event (principally heart failure hospitalization) or cardiovascular death, whichever came first.
Dapagliflozin reduced the primary outcome by 26% and reduced the risk of each of heart failure hospitalization and cardiovascular death individually, as well as overall mortality. Patient symptoms were also improved.
The aim of the present report was to examine the effect of dapagliflozin separately in patients with and without type 2 diabetes at baseline (45/55% split in the trial). The reason for this was that dapagliflozin was originally introduced as a glucose-lowering medication for the treatment of type 2 diabetes. We find that dapagliflozin was equally beneficial in patients with and without diabetes and was as well tolerated in patients without diabetes as in those with diabetes. More remarkably, among the patients without diabetes, dapagliflozin was as effective in participants with a completely normal glycated haemoglobin (HbA1c) as in those with prediabetes. In patients with a normal HbA1c, dapagliflozin did not lead to any reduction in HbA1c, but did improve clinical outcomes.