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Published on: February 18, 2022
SGLT2 inhibitors among patients with heart failure with preserved ejection fraction: A meta-analysis of randomised
Akash Jaiswal1, Vikash Jaiswal2, Song Peng Ang3
1Department of Geriatric Medicine, All India Institute of Medical Science, New Delhi, India.
Insights
Sodium-glucose co-transporter 2 (SGLT2) inhibitors significantly reduce heart failure hospitalizations. While effective for reducing cardiovascular events, SGLT2 inhibitors did not show a significant impact on all-cause mortality in this analysis.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Sodium-glucose co-transporter 2 (SGLT2) inhibitors are recommended for heart failure with reduced ejection fraction (HFrEF).
- Their efficacy in heart failure with preserved ejection fraction (HFpEF) remains debated.
- This analysis focuses on SGLT2 inhibitor effects in HFpEF, incorporating key trials like DELIVER and EMPEROR-Preserved.
Purpose of the Study:
- To evaluate the impact of SGLT2 inhibitors on patients with heart failure, specifically examining outcomes in HFpEF.
- To synthesize evidence from major clinical trials investigating SGLT2 inhibitors in this population.
Main Methods:
- A systematic literature search was conducted across PubMed, Embase, Scopus, and Cochrane libraries up to August 2022.
- Hazard ratios (HR) with 95% confidence intervals (CI) were calculated using a random-effects model.
- Statistical significance was determined by a P-value < .05 and CI not crossing 1.
Main Results:
- Six studies comprising 15,989 patients were analyzed.
- SGLT2 inhibitors significantly reduced composite cardiovascular mortality or first heart failure hospitalization (HR, 0.80 [95% CI: 0.74-0.87]) and heart failure hospitalizations (HR, 0.74 [95% CI: 0.67-0.82]).
- No significant difference was observed in all-cause mortality (HR, 0.97 [95% CI: 0.89-1.06]) or cardiovascular mortality (HR, 0.96 [95% CI: 0.82-1.13]).
Conclusions:
- SGLT2 inhibitors demonstrate significant benefits in reducing heart failure hospitalizations and composite cardiovascular events in the studied population.
- The observed benefits did not extend to a significant reduction in all-cause or cardiovascular mortality.
- These findings contribute to understanding the role of SGLT2 inhibitors in managing heart failure patients.
Background:
Sodium-glucose co-transporter 2 (SGLT2) inhibitors have been recommended in the practice guidelines for the treatment of patients with heart failure with reduced ejection fraction; however, their effects among patients with preserved ejection fraction have been debatable.
Objective:
We aim to evaluate the SGLT2 inhibitor effect among patients with heart failure with reduced ejection fraction, including DELIVER and EMPEROR-Preserved trials.
Methods:
We performed a systematic literature search using the PubMed, Embase, Scopus, and Cochrane libraries for relevant articles from inception until August 30th, 2022. Statistical analysis was performed by calculating hazard ratio (HR) using the random effect model with a 95% confidence interval (CI) and probability value (P). Statistical significance was met if 95% CI does not cross numeric "1" and P < .05.
Results:
Six studies with a total of 15,989 total patients were included in the final analysis. The mean age of patients enrolled in SGLT2 inhibitors and placebo was 69.13 and 69.37 years, respectively. The median follow-up duration was 2.24 years. SGLT2 inhibitors reduced composite cardiovascular mortality or first hospitalization for heart failure (HR, 0.80 [95% CI: 0.74-0.87], P < .001, I2 = 0%), heart failure hospitalization (HR, 0.74 [95% CI: 0.67-0.82], P < .001, I2 = 0%) compared with placebo. However, all-cause mortality (HR, 0.97 [95% CI: 0.89-1.06], P = .54, I2 = 0%) and cardiovascular mortality (HR, 0.96 [95% CI: 0.82-1.13), P = .66, I2 = 35.09%] were comparable between both groups.
Conclusion:
Our study finding shows that SGLT2 inhibitors significantly reduced the risk of first HF hospitalization or cardiovascular death and HF hospitalization; however, all-cause mortality was comparable between the groups.
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