Mo Weiming, Liu Jun, Zhang Zengyu, Yu Hong, Yang Aiping, Qu Fei, Hu Pingfang, Liu Zhuo, Hu Fengpei
a Department of Clinical Laboratory , Zhejiang Xiaoshan Hospital , Hangzhou , China.
b Department of Pediatrics , Xiaoshan First People's Hospital , Hangzhou , China.
Nord J Psychiatry. 2018 Apr;72(3):179-183. doi: 10.1080/08039488.2017.1410570. Epub 2017 Dec 7.
Autism spectrum disorder (ASD) is a group of developmental brain disorders caused by genetic and environmental factors. The objective of this study was to investigate whether single nucleotide polymorphisms (SNPs) in genes related to immune function were associated with ASD in Chinese Han children.
A total of 201 children with ASD and 200 age- and gender-matched healthy controls were recruited from September 2012 to June 2106. A TaqMan probe-based approach was used to genotype SNPs corresponding to rs28532698 and rs4301112 in CD157, rs855867 in AIM2, and rs2237126 in JARID2. Case-control and case-only studies were performed to determine the contribution of SNPs to the predisposition of disease and its severity, respectively.
Our results revealed that the genotypes and allele frequencies of these SNPs were not significantly associated with childhood ASD and its severity in this population.
Results of our study suggest that these SNPs are not predictors of childhood ASD in the Chinese Han population. The discrepant results suggest the predictor roles of SNPs have to be determined in different ethnic populations due to genetic heterogeneity of ASD.
自闭症谱系障碍(ASD)是一组由遗传和环境因素引起的发育性脑部疾病。本研究的目的是调查免疫功能相关基因中的单核苷酸多态性(SNP)是否与中国汉族儿童的ASD相关。
2012年9月至2016年6月共招募了201名ASD儿童和200名年龄及性别匹配的健康对照。采用基于TaqMan探针的方法对CD157中对应于rs28532698和rs4301112、AIM2中rs855867以及JARID2中rs2237126的SNP进行基因分型。分别进行病例对照研究和仅病例研究,以确定SNP对疾病易感性及其严重程度的影响。
我们的结果显示,在该人群中,这些SNP的基因型和等位基因频率与儿童ASD及其严重程度无显著相关性。
我们的研究结果表明,这些SNP不是中国汉族人群儿童ASD的预测指标。结果的差异表明,由于ASD的遗传异质性,SNP的预测作用必须在不同种族人群中确定。