AHA: Dapagliflozin Noninferior to Placebo for MACE in T2DM

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Treatment resulted in lower HF hospitalization rate in patients with, without atherosclerosis.
Treatment resulted in lower HF hospitalization rate in patients with, without atherosclerosis.

(HealthDay News) -- Treatment with dapagliflozin is noninferior to placebo for major adverse cardiovascular events (MACE) among patients with type 2 diabetes with or at risk for atherosclerotic cardiovascular disease, according to a study published online in the New England Journal of Medicine to coincide with the annual meeting of the American Heart Association, held from Nov. 10 to 12 in Chicago.

Stephen D. Wiviott, MD, from Brigham and Women's Hospital in Boston, and colleagues randomly assigned 17,160 patients with type 2 diabetes who had or were at risk for atherosclerotic cardiovascular disease (10,186 without) to receive dapagliflozin or placebo; participants were followed for a median of 4.2 years.

The researchers found that dapagliflozin was noninferior to placebo with respect to the primary safety outcome, a composite of MACE. In terms of efficacy, dapagliflozin did not result in a lower rate of MACE vs placebo (8.8 vs 9.4%; hazard ratio, 0.93; 95% confidence interval, 0.84 to 1.03; P=0.17) but was associated with a reduced rate of cardiovascular death or hospitalization for heart failure (4.9 vs 5.8%; hazard ratio, 0.83; 95% confidence interval, 0.73 to 0.95; P=0.005), reflecting a reduced rate of hospitalization for heart failure (hazard ratio, 0.73; 95 % confidence interval, 0.61 to 0.88).

"These new data suggest that in patients without established atherosclerotic cardiovascular disease, sodium-glucose cotransporter 2 inhibition can prevent serious clinical events, particularly hospitalization for heart failure," the authors write.

The trial was funded by AstraZeneca and Bristol-Myers Squibb; AstraZeneca is the manufacturer of dapagliflozin.

Reference

Wiviott SD, Raz I, Bonaca MP, etc. Dapagliflozin and Cardiovascular Outcomes in Type 2 Diabetes. N Engl J Med. DOI:10.1056/NEJMoa1812389

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