Dapagliflozin and cardiovascular outcomes in patients with Type 2 diabetes
Dalal Y Al-Bazz1, John Ph Wilding2,1
1Department of Diabetes and Endocrinology, Clinical Sciences Centre, Aintree University Hospital, Liverpool, L9 7AL, UK.
Abstract:
The relationship between cardiovascular disease, heart failure (HF) and Type-2 diabetes (T2DM) is widely recognized. Cardiovascular (CV) outcome trials are required for all new glucose-lowering agents to confirm safety with respect to CV risk. CV outcome trials with SGLT2i inhibitors have shown CV benefit, with reductions in major CV events and HF. This review focuses on the DECLARE-TIMI 58 trial with dapagliflozin in T2DM, which showed noninferiority for major adverse cardiovascular events and reduction in hospitalization for HF and associated CV mortality in a broad range of patients with T2DM. The DAPA-HF trial of dapagliflozin in people with HF with reduced ejection fraction with and without T2DM confirms benefits for those with HF.
Insights
Sodium-glucose co-transporter 2 inhibitors (SGLT2i) demonstrate cardiovascular benefits, including reduced heart failure (HF) hospitalizations. Dapagliflozin showed efficacy in Type-2 diabetes (T2DM) patients and those with HF, highlighting its role in managing cardiorenal risk.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Type-2 diabetes (T2DM) significantly increases cardiovascular disease (CVD) and heart failure (HF) risk.
- New glucose-lowering agents require cardiovascular (CV) outcome trials to assess CV risk.
- SGLT2 inhibitors have demonstrated notable CV benefits, including reduced HF events.
Purpose of the Study:
- To review the CV benefits of SGLT2 inhibitors, focusing on dapagliflozin.
- To analyze the DECLARE-TIMI 58 trial results for dapagliflozin in T2DM patients.
- To discuss the implications of dapagliflozin in HF management, referencing the DAPA-HF trial.
Main Methods:
- Review of pivotal clinical trials, including DECLARE-TIMI 58 and DAPA-HF.
- Analysis of data on major adverse cardiovascular events (MACE), HF hospitalizations, and CV mortality.
- Focus on dapagliflozin's efficacy in diverse patient populations with T2DM and/or HF.
Main Results:
- DECLARE-TIMI 58 showed dapagliflozin was noninferior for MACE and reduced HF hospitalizations and CV mortality in T2DM patients.
- DAPA-HF confirmed dapagliflozin's benefits in patients with HF with reduced ejection fraction, irrespective of T2DM status.
- SGLT2 inhibitors, particularly dapagliflozin, offer significant CV protection.
Conclusions:
- Dapagliflozin demonstrates a favorable CV safety profile and provides significant benefits in reducing HF events and mortality.
- The findings support the use of dapagliflozin in patients with T2DM and HF.
- SGLT2 inhibitors represent a crucial therapeutic class for managing cardiorenal risk in T2DM.
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