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SGLT2 inhibitor therapy in patients with advanced heart failure and reduced ejection fraction
Vincenzo Nuzzi1, Paolo Manca1, Francesca Parisi1
1Clinical Cardiology and Heart Failure Unit, Mediterranean Institute for Transplantation and Advanced Specialized Therapies (ISMETT), Palermo, Italy.
Insights
Sodium-glucose cotransporter inhibitors (SGLT2-i) show limited benefit in advanced heart failure with reduced ejection fraction (HFrEF). These SGLT2-i did not improve NTproBNP levels or clinical outcomes in advanced HFrEF patients, though they were well-tolerated.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Sodium-glucose cotransporter inhibitors (SGLT2-i) are established treatments for heart failure with reduced ejection fraction (HFrEF).
- Limited data exists on SGLT2-i efficacy in patients with advanced HFrEF.
Purpose of the Study:
- To evaluate the effect of SGLT2-i in advanced HFrEF compared to non-advanced HFrEF.
- To assess the impact of SGLT2-i on N-terminal pro-brain natriuretic peptide (NTproBNP) levels and clinical parameters in these populations.
Main Methods:
- A cohort of 105 HFrEF outpatients initiating SGLT2-i were divided into advanced and non-advanced HF groups.
- Primary outcome: NTproBNP trend. Secondary outcomes: New York Heart Association (NYHA) class, glomerular filtration rate (GFR), and left ventricular ejection fraction (LVEF) changes.
- Multivariate analysis assessed the association between advanced HF and NTproBNP reduction.
Main Results:
- Advanced HFrEF patients showed an increase in NTproBNP, while non-advanced patients had a significant reduction (-32%).
- Improvements in LVEF and NYHA class were observed only in the non-advanced group.
- Advanced HF diagnosis was independently associated with a lower probability of NTproBNP reduction (OR 0.041, p=0.031).
Conclusions:
- SGLT2-i do not significantly impact NTproBNP, LVEF, or NYHA class in patients with advanced HFrEF.
- SGLT2-i are well-tolerated in advanced HFrEF patients.
- Current evidence suggests SGLT2-i may not be as effective in advanced stages of HFrEF.
Aims:
Sodium-glucose cotransporter inhibitors (SGLT2-i) improve outcomes in patients with heart failure (HF) and reduced ejection fraction (HFrEF). However, evidence in patients with advanced HF is lacking. We aimed to determine the effect of SGLT2-i in advanced HFrEF compared to their effect on a non-advanced population.
Methods:
Consecutive HFrEF outpatients who started SGLT2-i were observed for 6-months. Patients were categorized as having advanced or non-advanced HFrEF. The primary outcome was the trend of NTproBNP in the two groups. Secondary outcomes included changes in New York Heart Association (NYHA) class, glomerular filtration rate (GFR), and ejection fraction (LVEF). The association between advanced HF diagnosis and including N-terminal pro-brain natriuretic peptide (NTproBNP) reduction was tested using multivariate analysis.
Results:
Overall, 105 patients (45 advanced, 60 non-advanced) were included. Mean age was 56 ± 10 years, 22 % were female, and 35 % had ischemic heart disease. Median NTproBNP at baseline for advanced and non-advanced patients was 1672pg/ml (IQR 520-3320) vs. 481 pg/ml (IQR 173-917), respectively (p < 0.001). At follow-up, only non-advanced patients reduced their NTproBNP (-32 % (95 % CI -51 to -3), p < 0.001), while advanced patients had an increase in NTproBNP. LVEF and NYHA class improved only in non-advanced patients. GFR was stable in both subgroups. At multivariate analysis a diagnosis of advanced HF was independently associated with a reduced probability of NTproBNP reduction (OR 0.041 (95 % CI 0.002-0.752), p = 0.031). Only one patient discontinued the drug due to side effects.
Conclusion:
In advanced HFrEF, SGLT2-i do not impact on NTproBNP, LVEF or NYHA class but are well tolerated.
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