ArticleExperimental and therapeutic medicine2021
Expression and significance of S-100β, CysC and NF-κB in patients with acute cerebral infarction.
Article in Experimental and therapeutic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 8 citations in OpenAlex.
- Development and validation of a dynamic nomogram for predicting in-hospital mortality in acute massive cerebral infarction: a retrospective study in a Chinese population.European journal of medical research · 2025Article
- Effect of oral ligustrazine phosphate with cerebroside carnosine on neurological function and serum inflammatory factors among patients with ischemic cerebrovascular disease: a quasi-experimental study.European journal of medical research · 2025Article
- Observational
- miR-124 Is Downregulated in Serum of Acute Cerebral Infarct Patients and Shows Diagnostic and Prognostic Value.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/HemostasisArticle
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2 authors at 1 institution in 1 country.
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Abstract
The present study aimed to explore the expression and significance of S100 protein β (S100β), cystatin C (CysC), and nuclear factor kappa B (NF-κB) in patients with acute cerebral infarction (ACI). ACI patients (n=120) were selected as the experimental group at Xuzhou Central Hospital from August 2016 to August 2018. Ninety healthy subjects who underwent a physical examination at Xuzhou Central Hospital during the same period were selected as the control group. The expression levels of S-100β, CysC and NF-κB were compared between the two groups. Serum S-100β, CysC and NF-κB levels were compared between ACI patients with different degree of nervous functional defects, different infarct size and different prognosis. ROC curve analysis was used for the diagnosis of ACI by serum S-100β, CysC and NF-κB levels. Serum S-100β, CysC and NF-κB levels in the experimental group were higher than those in the control group (P<0.05). The levels of serum S-100β, CysC and NF-κB in patients with different neurological deficits were significantly different. The levels of serum S-100β, CysC and NF-κB in the severe and medium type infarction group were significantly higher than those in the mild type infarction group (both P<0.05). The levels of serum S-100β, CysC and NF-κB in the severe type infarction group were higher than those in the medium type infarction group (P<0.05). There were significant differences in serum S-100β, CysC and NF-κB levels in patients with different infarct sizes. The levels of serum S-100β, CysC and NF-κB in patients with large and medium size infarction were higher than those in the small size infarction group (both P<0.05). The levels of serum S-100β, CysC and NF-κB in patients with large size infarction were higher than those in patients with medium size infarction (P<0.05). Serum S-100β, CysC and NF-κB levels in patients of the worsening group were significantly higher than those in patients of the non-worsening group. The levels of S-100β, CysC, NF-κB in ACI patients were significantly higher than those in healthy subjects. Increased levels of S-100β, CysC and NF-κB can be used as ideal indexes for diagnosing cerebral infarction and studying the condition.
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