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首页> 外文期刊>Psychoneuroendocrinology: An International Journal >Further investigations of the relation between polymorphisms in sex steroid related genes and autistic-like traits
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Further investigations of the relation between polymorphisms in sex steroid related genes and autistic-like traits

机译:性类固醇相关基因多态性与自闭型特征之间关系的进一步研究

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摘要

Autism spectrum disorders (ASDs) are more prevalent in boys than in girls, indicating that high levels of testosterone during early development may be a risk factor. Evidence for this hypothesis comes from studies showing associations between fetal testosterone levels, as well as indirect measures of prenatal androgenization, and ASDs and autistic-like traits (ALTs). In a recent study we reported associations between ALTs and single nucleotide polymorphisms (SNPs) in the genes encoding estrogen receptor 1 (ESR1), steroid-5-alpha-reductase, type 2 (SRD5A2) and sex hormone-binding globulin (SHBG) in a subset (n = 1771) from the Child and Adolescent Twin Study in Sweden (CATSS). The aim of the present study was to try to replicate these findings in an additional, larger, sample of individuals from the CATSS (n = 10,654), as well as to analyze additional SNPs of functional importance in SHBG and SRD5A2. No associations between the previously associated SNPs in the genes ESR1 and SRD5A2 and ALTs could be seen in the large replication sample. Still, our results show that two non-linked SNPs (rs6259 and rs9901675) at the SHBG gene locus might be of importance for language impairment problems in boys. The results of the present study do not point toward a major role for the investigated SNPs in the genes ESR1 and SRD5A2 in ALTs, but a possible influence of genetic variation in SHBG, especially for language impairment problems in boys, cannot be ruled out. (C) 2016 Elsevier Ltd. All rights reserved.
机译:自闭症谱系障碍(ASD)在男孩中比在女孩中更为普遍,这表明早期发育过程中睾丸激素水平升高可能是一个危险因素。该假设的证据来自研究,这些研究表明胎儿睾丸激素水平之间以及产前雄激素化的间接指标与ASD和自闭症样特征(ALT)之间存在关联。在最近的研究中,我们报道了ALTs与编码雌激素受体1(ESR1),甾体5α-还原酶,2型(SRD5A2)和性激素结合球蛋白(SHBG)的基因中的单核苷酸多态性(SNP)之间的关联。瑞典儿童和青少年双胞胎研究(CATSS)的一个子集(n = 1771)。本研究的目的是试图在CATSS(n = 10,654)的更大样本中复制这些发现,并分析在SHBG和SRD5A2中具有重要功能的其他SNP。在大型复制样本中,看不到基因ESR1和SRD5A2中先前关联的SNP与ALT之间的关联。尽管如此,我们的结果显示,SHBG基因位点的两个非连接SNP(rs6259和rs9901675)可能对男孩的语言障碍问题很重要。本研究的结果并未指出被调查的ALT中ESR1和SRD5A2基因中SNP的主要作用,但不能排除SHBG遗传变异的可能影响,尤其是男孩语言障碍问题。 (C)2016 Elsevier Ltd.保留所有权利。

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