Suppr超能文献

OAS2 rs739901 C/A 多态性与中国儿童 EV71 感染易感性有关。

Polymorphism of OAS2 rs739901 C/A Involves the Susceptibility to EV71 Infection in Chinese Children.

机构信息

Department of Pediatrics, the Affiliated Hospital of Qingdao University, Qirtgdao, 266000, China.

Department of Pediatrics, Zibo Maternal and Child Health Hospital, Zibo, 255029, China.

出版信息

Curr Med Sci. 2018 Aug;38(4):640-647. doi: 10.1007/s11596-018-1925-y. Epub 2018 Aug 20.

Abstract

This study aimed to assess the relationship of OAS2 rs739901 5,-flanking C/A polymorphisms with the susceptibility to Enterovirus-71 (EV71) infection. We investigated 294 hand-foot-mouth disease (HFMD) Chinese children with EV71 infection (165 mild cases and 129 encephalitis cases). The improved multiplex ligation detection reaction (iMLDR) technique was used to test the genotypes. In EV71-infected patients, the CA genotype distribution (P=0.007), A allele frequency (OR 1.32,95% CI 1.0-1.7, P=0.034) and CA+AA carriage frequency (P=0.003) of OAS2 rs739901 5'-flanking were obviously elevated as compared with controls, but there were no statistically significant differences between mild cases and encephalitis cases. In EV71-infected patients, the counts of white blood cells (P=0.034) and blood glucose concentrations (P=0.042) were raised in A carriers (CA+AA). Among different genotypes of encephalitis cases, the contents of cerebrospinal fluid (CSF) showed no significant differences. IFN-γ levels in EV71-infected patients were higher than those in controls (mild group vs. control group, P<0.01; encephalitis group vs. control group, P<0.01;). In encephalitis cases, IFN-γ levels were reduced (P<0.05) in A carriers compared to CC genotype, however, there were no significant differences between genotypes CA and AA (P=0.226). These findings suggest that OAS2 rs739901 5'-flanking C/A genetic polymorphisms involve the susceptibility to EV71 infection, and A allele might be a risk factor of the susceptibility to EV-71 infection.

摘要

本研究旨在评估 OAS2 rs739901 5'-侧翼 C/A 多态性与肠道病毒 71(EV71)感染易感性的关系。我们研究了 294 例手足口病(HFMD)中国儿童 EV71 感染(165 例轻症病例和 129 例脑炎病例)。采用改良多重连接检测反应(iMLDR)技术检测基因型。在 EV71 感染患者中,CA 基因型分布(P=0.007)、A 等位基因频率(OR 1.32,95%CI 1.0-1.7,P=0.034)和 CA+AA 携带频率(P=0.003)明显高于对照组,但轻症病例和脑炎病例之间无统计学差异。在 EV71 感染患者中,A 携带者(CA+AA)的白细胞计数(P=0.034)和血糖浓度(P=0.042)升高。在不同脑炎病例基因型中,脑脊液(CSF)含量无明显差异。EV71 感染患者 IFN-γ水平高于对照组(轻症组与对照组,P<0.01;脑炎组与对照组,P<0.01)。在脑炎病例中,与 CC 基因型相比,A 携带者的 IFN-γ水平降低(P<0.05),但 CA 和 AA 基因型之间无显著差异(P=0.226)。这些发现表明,OAS2 rs739901 5'-侧翼 C/A 遗传多态性与 EV71 感染易感性有关,A 等位基因可能是 EV-71 感染易感性的危险因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验