# Efficacy of sacubitril/valsartan sodium combined with simvastatin in treating chronic heart failure with arrhythmia and its effects on IL-6, IL-8, and TNF-α

**Authors:** Jingjing Li, Zhihua Wang

PMC · DOI: 10.5937/jomb0-59426 · Journal of Medical Biochemistry · 2026-01-06

## TL;DR

Combining sacubitril/valsartan sodium with simvastatin improves heart function and reduces inflammation in patients with chronic heart failure and arrhythmia.

## Contribution

The study demonstrates that combining sacubitril/valsartan sodium with simvastatin is more effective than monotherapy in treating chronic heart failure with arrhythmia.

## Key findings

- Combination therapy improved clinical efficacy, cardiac function, and reduced inflammatory markers more than simvastatin alone.
- The combination therapy group had fewer arrhythmia episodes and better lipid profiles.
- Adverse reactions were significantly lower in the combination therapy group.

## Abstract

To explore, in conjunction with clinical practice, the efficacy of different pharmacological treatment regimens for patients with chronic heart failure complicated by arrhythmia, and their effects on inflammatory factor levels.

A total of 96 patients with chronic heart failure and arrhythmia treated at our hospital from June 2022 to January 2025 were selected and randomly assigned by envelope method into a combination therapy group and a simvastatin group. The simvastatin group received simvastatin monotherapy, while the combination group was treated with sacubitril/valsartan sodium plus simvastatin. Clinical efficacy was compared between the two groups. Cardiac function, inflammatory factors, arrhythmia episodes, blood lipid levels, and oxidative stress markers were assessed before and after treatment. Adverse reactions in both groups were also observed.

The overall effective rate in the combination therapy group (93.75%) was significantly higher than that in the simvastatin group (72.92%) (c2= 7.500, P=0.006). After treatment, the combination group exhibited higher LVEF and lower LVESD and LVEDD levels compared to the simvastatin group (P&lt; 0.05). Serum levels of inflammatory factors (IL-6, IL-8, TNF-a) were significantly lower in the combination group than in the simvastatin group after treatment (P&lt; 0.05). Both the duration and frequency of arrhythmia episodes were reduced in the combination group compared to the simvastatin group (P&lt; 0.05). Post-treatment, LDL-C, TG, and TC levels were lower, and HDL-C was higher in the combination group than in the simvastatin group (P&lt; 0.05). MDA and SOD levels were also lower in the combination group after treatment (P&lt; 0.05). The incidence of adverse reactions was lower in the combination group (3.33%) compared to the simvastatin group (22.92%) (c2 = 5.352, P= 0.021).

For patients with chronic heart failure and arrhythmia, combined therapy with sacubitril/valsartan sodium and simvastatin demonstrates significant efficacy. It can alleviate inflammatory responses, improve cardiac function, reduce the frequency and duration of arrhythmia episodes, optimize lipid profiles and stress responses, and decrease adverse reactions. This approach is worthy of further clinical promotion.

## Linked entities

- **Chemicals:** simvastatin (PubChem CID 54454), IL-6 (PubChem CID 165368475), IL-8 (PubChem CID 169410440), TG (PubChem CID 2723601), TC (PubChem CID 23957), MDA (PubChem CID 1614)
- **Diseases:** arrhythmia (MONDO:0007263)

## Full-text entities

- **Genes:** MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Chronic heart failure (MESH:D006333), heart diseases (MESH:D006331), myalgia (MESH:D063806), myotoxicity (MESH:D000081030), rhabdomyolysis (MESH:D012206), myocardial ischemia (MESH:D017202), hypertrophy (MESH:D006984), cardiovascular death (MESH:D002318), dizziness (MESH:D004244), Arrhythmia (MESH:D001145), LVEDD (MESH:D018487), myocardial cell injury (MESH:D009202), chest tightness (MESH:D002637), ion channel abnormalities (MESH:C538353), metabolic (MESH:D008659), hypoxia (MESH:D000860), myocardial fibrosis (MESH:D005355), inflammatory (MESH:D007249), myocardial electrical instability (MESH:D064752), muscle weakness (MESH:D018908)
- **Chemicals:** Sacubitril (MESH:C000717211), lipid (MESH:D008055), Simvastatin (MESH:D019821), Valsartan (MESH:D000068756), calcium (MESH:D002118), H20000009 (-), sodium (MESH:D012964), TG (MESH:D013866), natriuretic peptide (MESH:D045265), MDA (MESH:D008315), cholesterol (MESH:D002784), TC (MESH:D013667), oxygen (MESH:D010100), MDA (MESH:D015104), aldosterone (MESH:D000450), TG (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12967194/full.md

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Source: https://tomesphere.com/paper/PMC12967194