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STAT3 单核苷酸多态性对儿童癫痫的影响。

The effect of single nucleotide polymorphisms of STAT3 on epilepsy in children.

机构信息

Department of Neurology, No. 1 People's Hospital of Jining, Jining, Shandong, China.

出版信息

Eur Rev Med Pharmacol Sci. 2020 Jan;24(2):837-842. doi: 10.26355/eurrev_202001_20067.

DOI:10.26355/eurrev_202001_20067
PMID:32016989
Abstract

OBJECTIVE

To investigate the effect of single nucleotide polymorphisms (SNPs) of signal transducer and activator of transcription 3 (STAT3) on epilepsy in children.

PATIENTS AND METHODS

A total of 169 children suffering from epilepsy admitted in No. 1 People's Hospital of Jining from July 2015 to December 2016 were enrolled as the research subjects. Immunohistochemistry and real time-PCR were used for analysis of the expression of STAT3 and p-STAT3 in epilepsy patients. The genotypes and alleles of rs1053005 and re744166 were analyzed through polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Statistical analysis was conducted to explore the correlation between the polymorphism of STAT3 and the incidence of epilepsy in children, and the polymorphism of STAT3 in the drug-resistant and non-resistant patients was compared.

RESULTS

Both the STAT3 and p-STAT3 were over-expressed in epilepsy patients. The GG genotype of rs1053005 was significantly lower in epilepsy patients than that of health control, p<0.05. By contrast, no significant difference was found in genotypes of rs744166 between epilepsy and healthy children. When comparing the genotypes of drug-resistant patients and that of non-resistant patients, the distribution of rs1053005 genotypes in the two groups showed a significant difference, p<0.05. No statistical difference was observed in rs744166 genotypes.

CONCLUSIONS

STAT3 polymorphism was associated with the risk of epilepsy and drug resistance to epilepsy. This study may provide a better understanding of STAT3 in epilepsy patients and provide new targets for the treatment of epilepsy patients.

摘要

目的

研究信号转导子和转录激活子 3(STAT3)单核苷酸多态性(SNP)对儿童癫痫的影响。

方法

选取 2015 年 7 月至 2016 年 12 月在济宁市第一人民医院就诊的 169 例癫痫患儿为研究对象,采用免疫组化和实时荧光定量 PCR 法分析癫痫患儿 STAT3 和 p-STAT3 的表达,采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)法分析 STAT3 的 rs1053005 和 re744166 基因型和等位基因。统计分析探讨 STAT3 多态性与儿童癫痫发病的相关性,并比较 STAT3 多态性与耐药和非耐药患儿的关系。

结果

癫痫患儿 STAT3 和 p-STAT3 均过表达。与健康对照组相比,癫痫患儿 rs1053005 的 GG 基因型明显降低,p<0.05。而癫痫患儿与健康儿童 rs744166 基因型无显著差异。耐药患儿与非耐药患儿 rs1053005 基因型分布比较,两组间基因型分布差异有统计学意义,p<0.05。rs744166 基因型在两组间无统计学差异。

结论

STAT3 多态性与癫痫的发病风险和癫痫耐药有关。本研究可能为了解癫痫患者的 STAT3 提供更好的依据,并为癫痫患者的治疗提供新的靶点。

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