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This Diabetes Drug Cuts Heart Failure Risk by 34%

In Health
August 30, 2019

LONDON:
The new type of drugs for type 2 diabetes — SGLT2 inhibitors — are associated with a reduced risk of heart failure by 34 per cent, researchers said.

The new SGLT2 inhibitors, which are now a commonly used drug group, reduce blood glucose, they added. In the study published in the journal The BMJ, the researchers wanted to show if there were positive cardiovascular effects from SGLT2 inhibitors in a broader patient group.

“There is cardiovascular benefit from SGLT2 inhibitors for a broader patient group in routine clinical care. This is an important result that we believe may be of interest to patients as well as drug authorities and doctors,” said study principal investigator Bjorn Pasternak, Associate Professor at the Karolinska Institutet in Sweden.

The researchers used several national registries containing data on drug use, diseases, cause of death and other data from close to 21,000 patients with type 2 diabetes who began treatment with SGLT2 inhibitors between April 2013 and December 2016. This information was then compared with an equal size matched population who began treatment with a different diabetes drug — DPP4 inhibitor.

The primary outcomes in the study were major cardiovascular events defined as myocardial infarction, stroke or cardiovascular death and hospital admission for heart failure. An important secondary outcome was death by any cause. In the primary analysis, the patients were monitored throughout the follow-up period, regardless of whether they had completed their treatment.

The researchers found that the use of SGLT2 inhibitors was associated with a reduced risk of heart failure but not with major cardiovascular events. The risk of heart failure was 34 per cent lower in the SGLT2 inhibitor group than in the DPP4 inhibitor group.

The use of SGLT2 inhibitors was also linked to a 20 per cent lower risk of death. The results are applicable primarily to dapaglifozin, which was the predominant SGLT2 inhibitor used in Scandinavia during the study period.