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Autism and KIR genes of the human genome: A brief meta-analysis

机译:人类基因组的自闭症和 KIR 基因:简要的荟萃分析

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Background Killer cell immunoglobin-like receptors (KIR) are the transmembrane glycoproteins on natural killer (NK) cells that regulate their functions. Studies show that immune system plays roles in neurodevelopmental disorders like autism, and NK cell abnormality can be a risk factor in autism spectrum disorders. Aim This study aims to investigate the role of KIR genes diversity in autism. Methods In order to find the relevant literature, we used PubMed, Google Scholar and other search engines. Association of each gene was analyzed through chi-square with Yate's correction (or Fisher's exact test if necessary). Software comprehensive meta-analysis was used. Both fixed and random effect models were reported. Results Among fourteen genes of KIR , the risk role of KIR2DS1 and KIR3DS1 were statistically significant based on fixed effect model. Among these two genes, KIR2DS1 needed random effect model because of its heterogeneity. After applying random effect, its role was not significant. The funnel plot showed no publication bias for KIR3DS1 , and its role was significant based on fixed effect model (P?=?.028; OR?=?1.31). Conclusions Autism spectrum disorders are accompanied by KIR3DS1 which is an activating gene of KIR . It seems that hyper-activity of NK cells results in inflammation in neuroimmune system that in turn can be associated with autism. The legend of 3DS1 receptor is unknown, and suggested to be investigated. This meta-analysis should be updated in future.
机译:背景杀伤细胞免疫球蛋白样受体(KIR)是天然杀伤(NK)细胞上的跨膜糖蛋白,可调节其功能。研究表明,免疫系统在自闭症等神经发育疾病中起作用,而NK细胞异常可能是自闭症谱系障碍的危险因素。目的本研究旨在研究KIR基因多样性在自闭症中的作用。方法为了找到相关文献,我们使用了PubMed,Google Scholar和其他搜索引擎。每个基因的关联性均通过卡方分析和Yate校正(或必要时采用Fisher精确检验)进行分析。使用软件综合荟萃分析。报告了固定效应模型和随机效应模型。结果在14个KIR基因中,基于固定效应模型,KIR2DS1和KIR3DS1的风险作用具有统计学意义。在这两个基因中,KIR2DS1由于其异质性需要随机效应模型。应用随机效应后,其作用不明显。漏斗图没有显示出KIR3DS1的发布偏倚,并且根据固定效应模型,其作用很显着(P?=?0.028; OR?=?1.31)。结论自闭症谱系障碍伴有KIR3DS1,它是KIR的激活基因。似乎NK细胞的过度活跃导致神经免疫系统的炎症,而炎症又可能与自闭症有关。 3DS1受体的图例是未知的,建议进行调查。该荟萃分析应在将来进行更新。

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