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Toll 样受体 2 多态性与缺血性脑卒中患者国立卫生研究院卒中量表评分的相关性。

Association of Toll-like receptor 2 polymorphisms with National Institute of Health Stroke Scale scores of ischemic stroke patients.

机构信息

Kohwang Medical Research Institute, School of Medicine, Kyung Hee University, Seoul, South Korea.

出版信息

J Mol Neurosci. 2012 Mar;46(3):536-40. doi: 10.1007/s12031-011-9640-1. Epub 2011 Sep 2.

Abstract

Toll-like receptor 2 (TLR2) has been shown to have an important role in the postischemic inflammatory response and to contribute to ischemic brain damage. In this study, we investigated whether coding region single nucleotide polymorphisms (SNPs) of the TLR2 gene were associated with ischemic stroke (IS) and with clinical phenotypes in IS patients. We genotyped two SNPs (rs3804099 [Asn199Asn] and rs3804100 [Ser450Ser]) using direct sequencing in 202 IS patients and 291 control subjects. No SNPs of the TLR2 gene were found to be associated with IS. However, in analysis of clinical phenotypes, we found that rs3804099 was associated with the National Institute of Health Stroke Scale (NIHSS) scores of IS patients in codominant (TC vs. TT, p = 0.0005; CC vs. TT, p = 0.0007) and dominant models (TC/CC vs. TT, p = 0.0001). Also, rs3804100 revealed significant association in codominant (TC vs. TT, p = 0.0002; CC vs. TT, p = 0.008) and dominant models (TC/CC vs. TT, p < 0.0001). In allele frequency analysis, we also found that the C alleles of rs3804099 and rs3804100 were associated with higher NIHSS scores (p = 0.0003 in rs3804099; p = 0.0001 in rs3804100). Our results suggest that TLR2 may be related to severe IS.

摘要

Toll 样受体 2(TLR2)已被证明在缺血后炎症反应中具有重要作用,并有助于缺血性脑损伤。在这项研究中,我们研究了 TLR2 基因编码区单核苷酸多态性(SNP)是否与缺血性脑卒中(IS)和 IS 患者的临床表型相关。我们使用直接测序法对 202 例 IS 患者和 291 例对照进行了 TLR2 基因的两个 SNP(rs3804099 [Asn199Asn]和 rs3804100 [Ser450Ser])的基因分型。TLR2 基因的 SNP 与 IS 无关。然而,在临床表型分析中,我们发现 rs3804099 与 NIHSS 评分呈显著相关(TC 与 TT 相比,p=0.0005;CC 与 TT 相比,p=0.0007),并且 rs3804099 与显性模型(TC/CC 与 TT 相比,p=0.0001)也呈显著相关。此外,rs3804100 在显性模型(TC 与 TT 相比,p=0.0002;CC 与 TT 相比,p=0.008)和显性模型(TC/CC 与 TT 相比,p<0.0001)中也存在显著相关性。在等位基因频率分析中,我们还发现 rs3804099 和 rs3804100 的 C 等位基因与 NIHSS 评分升高相关(rs3804099 中 p=0.0003;rs3804100 中 p=0.0001)。我们的研究结果表明,TLR2 可能与严重的 IS 有关。

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