# Clinical application of butylphthalide sequential therapy on PTX-3, S100B, IL-6 in acute cerebral infarction

**Authors:** Pin Meng, Jianyu Zhang, Jiaojiao Li, Niu Ji, Xinyu Zhou, Bingchao Xu

PMC · DOI: 10.5937/jomb0-57276 · Journal of Medical Biochemistry · 2025-10-28

## TL;DR

This study shows that butylphthalide sequential therapy improves outcomes in patients with acute cerebral infarction and cognitive dysfunction.

## Contribution

The study introduces butylphthalide sequential therapy as a novel treatment for acute cerebral infarction with cognitive dysfunction.

## Key findings

- Butylphthalide therapy reduced inflammatory markers like PTX-3, IL-6, and hs-CRP in ACI patients.
- Patients receiving butylphthalide showed better cognitive and neurological outcomes compared to controls.
- The therapy was associated with fewer complications and improved quality of life.

## Abstract

Acute cerebral infarction (ACI) is a frequent type of stroke disease in clinical practice. Cognitive dysfunction is a common complication of ACI, which severely influences the quality of life of patients. Objective: To evaluate the effects of butylphthalide sequential therapy on inflammatory markers (PTX-3, S100B, IL-6) and cognitive outcomes in patients with acute cerebral infarction (ACI).

From March 2023 to March 2024, 120 patients with ACI combined with cognitive dysfunction diagnosed and treated in our hospital were randomly divided into a control group (CG) and an observation group (OG). The clinical effective rate, MMSE scores, NIHSS scores, Barthel index scores, levels of inflammatory factors, and incidence of complications in both groups were compared.

Compared to the CG, the total effective rate of the OG was higher (c2=4.90, P&lt;0.05). MMSE scores and Barthel index scores were elevated in both groups 2 weeks and 2 months after treatment, and those in the OG were higher relative to the CG (P&lt;0.05). NIHSS scores and hs-CRP, as well as PTX-3 levels, declined in both groups 2 weeks and 2 months after treatment, and those in the OG were lessened compared to the CG (P&lt;0.05). The occurrence of complications in the OG was reduced relative to the CG (P&lt;0.05). Serum analysis showed lower hs-CRP, PTX-3, and IL-6 levels in the OG (P&lt;0.05), suggesting reduced inflammation with butylphthalide therapy. While S100B levels showed a non-significant decline, albumin levels remained unchanged, indicating no significant impact on neuronal injury or nutritional recovery (P&gt;0.05).

Butylphthalide sequential therapy can promote the neurological function as well as living ability of patients with ACI combined with cognitive dysfunction, with high safety, which is valuable for clinical promotion.

## Linked entities

- **Proteins:** PTX3 (pentraxin 3), S100B (S100 calcium binding protein B), IL6 (interleukin 6)
- **Chemicals:** butylphthalide (PubChem CID 61361)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, S100B (S100 calcium binding protein B) [NCBI Gene 6285] {aka NEF, S100, S100-B, S100beta}, PTX3 (pentraxin 3) [NCBI Gene 5806] {aka TNFAIP5, TSG-14}
- **Diseases:** inflammation (MESH:D007249), Cognitive dysfunction (MESH:D003072), ACI (MESH:D056989), neuronal injury (MESH:D009410), stroke disease (MESH:D020521)
- **Chemicals:** Butylphthalide (MESH:C027125)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12639508/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12639508/full.md

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Source: https://tomesphere.com/paper/PMC12639508