# Efficacy and influencing factors analysis of SGLT2 inhibitors in treating heart failure following acute myocardial infarction

**Authors:** Haiping Du, Hui Xu, Jinwei Bao

PMC · DOI: 10.3389/fphar.2025.1693420 · Frontiers in Pharmacology · 2025-10-30

## TL;DR

This study shows that SGLT2 inhibitors improve heart function and reduce stress markers in heart failure patients after a heart attack, better than traditional treatments.

## Contribution

The study identifies baseline LVEF and NT-proBNP as predictors of SGLT2 inhibitor efficacy in post-AMI heart failure.

## Key findings

- SGLT2 inhibitors improved LVEF and reduced NT-proBNP, troponin I, and hs-CRP levels significantly compared to conventional treatments.
- The overall effectiveness rate was 88% for SGLT2 inhibitors versus 75.71% for conventional treatments.
- Lower baseline LVEF and higher NT-proBNP levels predicted better outcomes with SGLT2 inhibitors.

## Abstract

Heart failure (HF) following acute myocardial infarction (AMI) significantly impacts morbidity and mortality. Sodium-glucose co-transporter 2 (SGLT2) inhibitors, initially developed for type 2 diabetes mellitus, have shown cardiovascular benefits. This study evaluates the efficacy of SGLT2 inhibitors in treating HF post-AMI compared to conventional treatments.

We conducted a retrospective cohort study at our hospital from September 2022 to September 2024 involving 315 patients with HF post-AMI. Patients were categorized into a conventional treatment group (n = 140) and an SGLT2 inhibitor group (n = 175), with the latter further divided into effective (n = 154) and ineffective (n = 21) subgroups. Cardiac function was assessed pre- and post-treatment using echocardiography and serum biomarkers. Baseline characteristics and potential predictors of SGLT2 efficacy were also analyzed.

The SGLT2 group exhibited significant improvements in left ventricular ejection fraction (LVEF), decreased NT-proBNP, troponin I, and hs-CRP levels compared to the conventional group (P < 0.001). The overall effectiveness rate was 88.00% versus 75.71% in the conventional group (P = 0.004). Lower baseline LVEF and higher NT-proBNP levels were significant predictors of better outcomes. Notably, adverse reactions such as angina were reduced in the SGLT2 group.

SGLT2 inhibitors were associated with enhanced cardiac function and reduce cardiac stress markers in HF patients post-AMI, suggesting their potential as an adjunctive therapy. Lower baseline LVEF and higher NT-proBNP levels may predict better response, suggesting their utility in personalized treatment strategies. This was a retrospective single-center study, and further prospective trials are needed to confirm these findings.

## Linked entities

- **Proteins:** LOC105904758 (troponin I, fast skeletal muscle-like)
- **Diseases:** heart failure (MONDO:0005252), acute myocardial infarction (MONDO:0004781), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** type 2 diabetes mellitus (MESH:D003924), AMI (MESH:D009203), angina (MESH:D000787), HF (MESH:D006333)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12611968/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12611968/full.md

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Source: https://tomesphere.com/paper/PMC12611968