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中国汉族人群中神经损伤诱导蛋白基因2多态性与中风的关系。

Relationship between nerve injury-induced protein gene 2 polymorphism and stroke in Chinese Han population.

作者信息

Wang Xin, Zhang Jianying, Liu Yi, Zhang Yingdong

机构信息

Department of Neurology, Medical School of Nanjing Medical University, Nanjing, Jiangsu 210029, China;

出版信息

J Biomed Res. 2011 Jul;25(4):287-91. doi: 10.1016/S1674-8301(11)60039-0.

Abstract

The aim of present study was to investigate the relationship between nerve injury-induced protein 2 (NINJ2) gene polymorphism and stroke in Chinese Han population. Fifty-two patients with large-artery atherosclerosis (LAA) infarction, 85 patients with small-artery occlusion lacunar (SAO) infarction, 50 patients with intracerebral hemorrhage (ICH) and 66 controls were included. Genotypes and alleles frequencies of the two single nucleotide polymorphisms (SNPs) of NINJ2 among different groups were analyzed and compared. In regard to rs12425791, the frequencies of the AG and AA+AG genotypes of the LAA and SAO groups were significantly higher than those in the control group; the frequency of the A allele of the SAO group was significantly higher than that of the control group. In regard to rs11833579, there were not any significant differences between the case and the control groups. The SNP rs12425791 is significantly associated with ischemic stroke, and the A allele increases the susceptibility to stroke. The SNP rs11833579 is not significantly associated with stroke.

摘要

本研究旨在探讨神经损伤诱导蛋白2(NINJ2)基因多态性与中国汉族人群中风的关系。纳入52例大动脉粥样硬化(LAA)梗死患者、85例小动脉闭塞性腔隙性(SAO)梗死患者、50例脑出血(ICH)患者和66例对照。分析并比较不同组间NINJ2两个单核苷酸多态性(SNP)的基因型和等位基因频率。对于rs12425791,LAA组和SAO组的AG以及AA + AG基因型频率显著高于对照组;SAO组的A等位基因频率显著高于对照组。对于rs11833579,病例组与对照组之间无显著差异。SNP rs12425791与缺血性中风显著相关,且A等位基因增加中风易感性。SNP rs11833579与中风无显著关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1531/3597068/53c7e7fc30b7/jbr-25-04-287-g001.jpg

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