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MAPK1基因多态性及mRNA表达与缺血性脑卒中神经功能缺损程度的相关分析▲
Correlation between MAPK1 gene polymorphisms and mRNA expression and the degree of neurological deficits in patients with ischemic stroke

内科 201914卷02期 页码:125-128+141

作者机构:广西医科大学公共卫生学院流行病学教研室,南宁市530021

基金信息:▲基金项目:国家自然科学基金项目(81473670,81573756)
*通信作者:苏莉,广西医科大学公共卫生学院流行病学教研室,电子邮箱 suli2018@hotmail.com

DOI:10.16121/j.cnki.cn45-1347/r.2019.02.01

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  • 英文简介
  • 参考文献
目的探讨丝裂原活化蛋白激酶1(MAPK1)基因rs6928、rs13515、rs1063311多态性及MAPK1基因mRNA表达与缺血性脑卒中(IS)患者神经功能缺损严重程度的相关性。方法采用Massarray SNP基因分型技术对MAPK1基因的rs6928、rs13515、rs1063311多态性进行基因分型,运用qRT-PCR实验技术测定MAPK1基因mRNA表达水平,使用NIHSS量表对IS患者进行神经功能缺损评分。结果校正性别、年龄之后,在加性模型、隐性模型中,rs6928多态性与IS患者NIHSS评分具有相关性(P<0.05)。MAPK1基因mRNA表达水平与IS患者NIHSS评分无相关性(P>0.05)。结论MAPK1基因rs6928多态性可能会影响IS患者神经功能缺损的严重程度。
ObjectiveTo investigate the correlation between polymorphisms of mitogen-activated protein kinases 1(MAPK1)gene rs6928, rs13515 and rs1063311 and MAPK1 mRNA expression and the degree of neurological deficits in patients with ischemic stroke(IS). MethodsGenotypes of MAPK1 gene rs6928, rs13515 and rs1063311 were detected using Massarray SNP genotyping technique, MAPK1 mRNA expression was assessed by qRT-PCR, and the degree of neurological deficits in patients with IS was evaluated using NIHSS score. ResultsAfter adjusting for gender and age, the polymorphisms of rs6928 was associated with NIHSS score in patients with IS in the additive model and recessive model(P<0.05). The MAPK1 mRNA expression was not correlated to NIHSS score in IS patients (P>0.05). ConclusionThe polymorphism of MAPK1 gene rs6928 may affect the degree of neurological deficits in patients with IS.

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