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首页> 外文期刊>Autism research: official journal of the International Society for Autism Research >SHANK1 SHANK1 polymorphisms and SNP–SNP interactions among SHANK SHANK family: A possible cue for recognition to autism spectrum disorder in infant age
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SHANK1 SHANK1 polymorphisms and SNP–SNP interactions among SHANK SHANK family: A possible cue for recognition to autism spectrum disorder in infant age

机译:Shank1 Shank1柄柄之间的多态性和SNP-SNP相互作用:婴儿年龄识别自闭症谱系障碍的可能提示

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摘要

Autism spectrum disorder (ASD) is a serious lifelong neurodevelopmental disorder. ASD is diagnosed for children at the age of two. ASD diagnosis, as early as possible, lays the foundation for treatment and much better prognosis. Notably, gene‐based test is an inherent method to recognize the potential infants with ASD before the age of two. To investigate whether SHANK family contributes to ASD prediction, on the basis of our previous studies of SHANK2 and SHANK3 , we further investigated associations between SHANK1 polymorphisms and ASD risk as well as SNP–SNP interactions among SHANK family. We enrolled 470 subjects (229 cases and 241 healthy controls) who were northeast Chinese Han. Four tag SNPs (rs73042561, rs3745521, rs4801846, and rs12461427) of SHANK1 were selected and genotyped. We used the SNPStats online analysis program to assess the associations between the four SNPs and ASD risk. The SNP–SNP interactions among SHANK family were analyzed using multifactor dimensionality reduction method. We found that the four SHANK1 SNPs were not associated with ASD risk in northeast Chinese Han population. There existed a strong synergistic interaction between rs11236697 [ SHANK2 ] and rs74336682 [ SHANK2 ], and moderate synergistic interactions (rs74336682 [ SHANK2 ]–rs73042561 [ SHANK1 ], rs11236697 [ SHANK2 ]–rs77716438 [ SHANK2 ], and rs11236697 [ SHANK2 ]–rs75357229 [ SHANK2 ]). These SHANK1 variants may not affect the susceptibility to ASD in Chinese Han population. SNP–SNP interactions in SHANK family may confer ASD risk. Autism Res 2019, 12: 375–383 ? 2019 International Society for Autism Research, Wiley Periodicals, Inc. Lay Summary ASD is a serious lifelong neurodevelopmental disorder with strong genetic components. We investigated associations between SHANK1 polymorphisms and ASD risk as well as SNP–SNP interactions among SHANK family. Our results indicated that there exists no association between SHANK1 SNPs and ASD, and SNP–SNP interactions in SHANK family may confer ASD risk in the Northeast Han Chinese population. Future studies are needed to test more SHANK family SNPs in a large sample to demonstrate the associations.
机译:自闭症谱系障碍(ASD)是一种严重的终身神经发育障碍。 ASD被诊断为2岁的儿童。尽早诊断,为治疗和更好的预后奠定基础。值得注意的是,基于基因的测试是一种固有的方法,可以在两岁之前识别ASD的潜在婴儿。为了调查柄部是否有助于朝向ASD预测,在我们对Shank2和Shank3的先前研究的基础上,我们进一步调查了Shank1多态性和ASD风险之间的关联以及柄族之间的SNP-SNP相互作用。我们注册了470名科目(229例,241例健康控制),他是中国东北汉族。选择Shank1的四个标签SNPS(RS73042561,RS3745521,RS4801846和RS461427)和基因分型。我们使用SNPSTATA在线分析计划来评估四个SNP和ASD风险之间的关联。利用多因素维数减少方法分析柄族之间的SNP-SNP相互作用。我们发现,四个Shank1 SNP与东北汉族人口的ASD风险无关。 Rs11236697 [Shank2]和RS74336682 [Shank2]之间存在强大的协同相互作用(RS74336682 [Shank2] -RS73042561 [Shank1],RS1123669738 [Shank2]和RS11236697 [Shank2] -RS75357229 [ shank2])。这些Shank1变体可能不会影响中国汉族人群对ASD的易感性。 Shank系列中的SNP-SNP相互作用可能会授予ASD风险。自闭症es 2019,12:375-383? 2019年国际自闭症研究协会,Wiley期刊,Inc。Lay概要ASD是一种严重的终身神经发育障碍,具有强大的遗传成分。我们调查了Shank1多态性和ASD风险的关联以及柄部中的SNP-SNP相互作用。我们的结果表明,SHANK1 SNP和ASD之间没有关联,SHANK系列中的SNP-SNP互动可能会在东北汉族人群中授予ASD风险。未来的研究需要在大型样品中测试更多的柄族SNP以展示协会。

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  • 作者单位

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Chunguang Rehabilitation HospitalChangchun Jilin China;

    The Key Laboratory of Molecular Epigenetics of Ministry of Education Institute of Cytology and;

    Institute of Translational MedicineThe First Hospital of Jilin UniversityChangchun Jilin China;

    Institute of Translational MedicineThe First Hospital of Jilin UniversityChangchun Jilin China;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

    Department of Epidemiology and Biostatistics School of Public HealthJilin UniversityChangchun;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经病学与精神病学;
  • 关键词

    autism spectrum disorder; SHANK1; SHANK2; SHANK3; Single nucleotide polymorphisms; SNP–SNP interaction;

    机译:自闭症谱系;Shank1;shank2;shank3;单核苷酸多态性;snp-snp互动;

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