# Differential cardiovascular benefits of SGLT2 inhibitors, sacubitril/valsartan, omecamtiv mecarbil, and vericiguat across heart failure phenotypes: a systematic review and meta-analysis

**Authors:** Meng Wang, Zhihong Zuo, Ting Wu, Zijing Zhou

PMC · DOI: 10.3389/fphar.2026.1644757 · Frontiers in Pharmacology · 2026-02-06

## TL;DR

This study compares how different heart failure drugs affect patients with various heart failure types, finding that SGLT2 inhibitors work well across all types, while other drugs have mixed results.

## Contribution

The study provides a systematic comparison of drug benefits and risks across heart failure subtypes using a meta-analysis.

## Key findings

- SGLT2 inhibitors significantly reduce cardiovascular death and hospitalization across all heart failure types.
- Sacubitril/valsartan improves outcomes in HFrEF but increases hypotension risk in HFmrEF/HFpEF.
- Omecamtiv mecarbil and vericiguat show limited evidence of benefit.

## Abstract

The study evaluated the cardiovascular outcomes associated with pharmacological treatments in heart failure (HF) patients and explored whether the benefits/risks associated with these drugs for HF with mildly reduced or preserved ejection fraction (HFmrEF/HFpEF) were consistent with HF with reduced EF (HFrEF).

Several online databases were searched. All studies explored the cardiovascular effects of sodium glucose cotransporter-2 inhibitor (SGLT2i), sacubitril/valsartan, omecamtiv mecarbil and vericiguat were screened and reviewed.

A total of 39 studies were included. Compared with placebo therapy, SGLT2i significantly reduced cardiovascular death and hospitalization for HF (HHF) in both HFrEF and HFmrEF/HFpEF patients (approximately 13%–27% risk reduction). SGLT2i reduced serious adverse events across all HF types. Sacubitril/valsartan demonstrated significant benefits in HFrEF patients, reducing cardiovascular death by 19%, all-cause mortality by 22%, and HHF by 22%. However, these benefits were not observed in HFmrEF/HFpEF patients. In contrast, sacubitril/valsartan substantially increased hypotension risk in HFmrEF/HFpEF patients. Omecamtiv mecarbil and vericiguat tended to improve cardiovascular outcomes in patients with HF, but the difference was not statistically significant.

SGLT2i represents an effective and safe treatment strategy across the HF spectrum. Sacubitril/valsartan significantly improves outcomes in HFrEF but requires careful benefit-risk evaluation in HFmrEF/HFpEF patients. Current evidence does not support routine use of omecamtiv mecarbil or vericiguat. Large-scale randomized trials are warranted to validate these findings.

CRD42023455966.

## Linked entities

- **Chemicals:** sacubitril/valsartan (PubChem CID 24755620), omecamtiv mecarbil (PubChem CID 11689883), vericiguat (PubChem CID 54674461)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, MYH14 (myosin heavy chain 14) [NCBI Gene 79784] {aka DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C}, SGCB (sarcoglycan beta) [NCBI Gene 6443] {aka A3b, LGMD2E, LGMDR4, SGC}
- **Diseases:** toxicity (MESH:D064420), cardiomyocyte hypertrophy (MESH:D006984), atrial fibrillation (MESH:D001281), hypoglycemia (MESH:D007003), Cardiovascular death (MESH:D002318), CKD (MESH:D012080), Death (MESH:D003643), hypertension (MESH:D006973), stiffness (MESH:C566112), microvascular dysfunction (MESH:D017566), Angioedema (MESH:D000799), HFpEF (MESH:D054144), HFmrEF (MESH:D054143), systolic dysfunction (MESH:D006331), Diabetic ketoacidosis (MESH:D016883), ventricular remodeling (MESH:D020257), HF (MESH:D006333), cardiac arrest (MESH:D006323), diabetes (MESH:D003920), endothelial dysfunction (MESH:D014652), Hyperkalemia (MESH:D006947), fibrosis (MESH:D005355), Hypotension (MESH:D007022), sudden cardiac death (MESH:D016757), diastolic dysfunction (MESH:D018487)
- **Chemicals:** fatty acid (MESH:D005227), natriuretic peptide (MESH:D045265), Omecamtiv mecarbil (MESH:C547293), perindopril (MESH:D020913), NO (MESH:D009614), Omecamtiv (-), calcium (MESH:D002118), valsartan (MESH:D000068756), lipid (MESH:D008055), Sacubitril (MESH:C000717211), spironolactone (MESH:D013148), Vericiguat (MESH:C000603960), uric acid (MESH:D014527), candesartan (MESH:C081643), cGMP (MESH:D006152)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12920234/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12920234/full.md

## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920234/full.md

---
Source: https://tomesphere.com/paper/PMC12920234