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SGLT2i‑treated heart failure patients with a reduced ejection fraction: A meta‑analysis
1Department of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
Insights
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) significantly reduce hospitalization for heart failure (HF) and cardiovascular death in patients with reduced ejection fraction. These benefits apply to patients with or without diabetes, highlighting SGLT2i as a key therapy for HF management.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Heart failure (HF) with reduced ejection fraction (HFrEF) is a major cause of morbidity and mortality.
- Identifying effective therapeutic strategies for HFrEF is crucial, especially for patients with or without diabetes mellitus.
Purpose of the Study:
- To systematically review and meta-analyze the effects of Sodium-glucose cotransporter 2 inhibitors (SGLT2i) on cardiovascular outcomes in patients with HFrEF.
- To assess the impact of SGLT2i on HF hospitalization, cardiovascular death, and all-cause mortality in this patient population.
Main Methods:
- A systematic review of randomized controlled trials (RCTs) comparing SGLT2i with placebo in HFrEF patients was performed.
- Studies were identified through comprehensive searches of PubMed, Web of Science, and EMBASE databases up to July 2021.
- Pooled effects were estimated using odds ratios (OR) and 95% confidence intervals (CI) with fixed- or random-effects models, and sensitivity analyses were conducted.
Main Results:
- Five RCTs involving HFrEF patients were included in the meta-analysis.
- SGLT2i significantly reduced the risk of hospitalization for HF/cardiovascular death (OR=0.72), cardiovascular death (OR=0.84), hospitalization for HF (OR=0.69), and all-cause mortality (OR=0.79) compared to placebo.
- Results were consistent across sensitivity analyses, indicating the robustness of the findings.
Conclusions:
- SGLT2 inhibitors are effective in reducing the risk of HF hospitalization, cardiovascular death, and all-cause mortality in patients with HFrEF.
- The beneficial effects of SGLT2i extend to patients with HFrEF irrespective of their diabetes status.
- These findings support the use of SGLT2i as a foundational therapy for managing HFrEF.
Abstract:
The aim of this study was to investigate the effects of SGLT2 inhibitors (SGLT2i) on patients with heart failure (HF) and reduced ejection fraction, with or without diabetes. A systematic review of randomized controlled trials (RCTs) was conducted, comparing SGLT2i to a placebo for HF patients. Relevant studies from PubMed, Web of Science, and EMBASE were searched from inception to July 2021, without any language restrictions. The pooled effect was estimated using the odds ratio (OR) and 95% confidence interval (CI). Depending on the heterogeneity test results, either random effects or fixed effects models were selected to estimate the pooled effects. Sensitivity analysis was conducted by gradually removing each study to evaluate the results' stability. A total of 5 RCT studies were included in the analysis. The fixed-effects model demonstrated that the patients in the SGLT2i group had a lower risk of hospitalization for HF/cardiovascular death (OR=0.72; 95% CI, 0.67-0.78), P<0.0001; I2=0.0%, P=0.966), cardiovascular death (OR=0.84, 95% CI (0.77, 0.93), P<0.0001; I2=0.0%, P=0.633), hospitalization for HF (OR=0.69, 95% CI (0.63, 0.75), P<0.0001; I2=0.0%, P=0.933), and all-cause mortality (OR=0.79, 95% CI (0.71, 0.89), P<0.0001; I2=3.3%, P=0.376) compared to the placebo group. Sensitivity analysis showed that the pooled effect value remained stable within the corresponding range, even after each study was gradually removed. In conclusion, SGLT2i can reduce the risk of HF hospitalization, cardiovascular death, and all-cause mortality in patients with HF and a reduced ejection fraction, regardless of the presence or absence of diabetes.
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