Qiu Shuang, Li Yan, Li Yong, Zhong Weijing, Shi Meijuan, Zhao Qian, Zhang Kaixin, Wang Yihan, Lu Meihan, Zhu Xiaojuan, Jiang Huiyi, Yu Yaqin, Cheng Yi, Liu Yawen
Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun 130021, Jilin, China.
Chunguang Rehabilitation Hospital, Changchun 130012, Jilin, China.
Gene. 2018 Apr 20;651:100-105. doi: 10.1016/j.gene.2018.01.078. Epub 2018 Feb 7.
Autism spectrum disorder (ASD), as one of neurodevelopmental disorders, affects about 1/160 of people worldwide. The etiology and pathogenesis of ASD remain elusive. Synapses are essential components of neurons and basic information transmission unit in the nervous system, adjusting behavior to environmental stimuli and controlling body functions, memories, and emotions. SHANK3 is one of the synapse genes which play important roles in maintaining synaptic structure and function. SHANK3 has been researched as a probably susceptibility gene for ASD. We investigated the association between polymorphisms in SHANK3 and ASD in the Northeast Han Chinese population. A total of 470 subjects (229 cases and 241 controls) were enrolled in our case-control study. Five single nucleotide polymorphisms (SNPs) (rs756638, rs4824116, rs76268556, rs9616915, and rs75767639) in SHANK3 were selected and genotyped. Our study did not identify a significant association of SHANK3 SNPs with ASD in the Northeast Han Chinese population. Future studies need to test more SHANK3 SNPs in large sample to demonstrate the association between SNPs in SHANK3 and ASD.
自闭症谱系障碍(ASD)作为神经发育障碍之一,影响着全球约1/160的人口。ASD的病因和发病机制仍不清楚。突触是神经元的重要组成部分,也是神经系统中基本的信息传递单元,可根据环境刺激调整行为,并控制身体功能、记忆和情绪。SHANK3是在维持突触结构和功能中起重要作用的突触基因之一。SHANK3已被作为ASD的一个可能的易感基因进行研究。我们调查了中国东北汉族人群中SHANK3基因多态性与ASD之间的关联。我们的病例对照研究共纳入了470名受试者(229例病例和241名对照)。选择并对SHANK3基因中的五个单核苷酸多态性(SNP)(rs756638、rs4824116、rs76268556、rs9616915和rs75767639)进行基因分型。我们的研究未发现中国东北汉族人群中SHANK3基因SNP与ASD之间存在显著关联。未来的研究需要在大样本中检测更多的SHANK3基因SNP,以证明SHANK3基因SNP与ASD之间的关联。