Zettergren Anna, Karlsson Sara, Hovey Daniel, Jonsson Lina, Melke Jonas, Anckarsäter Henrik, Lichtenstein Paul, Lundström Sebastian, Westberg Lars
Institute of Neuroscience and Physiology, Department of Pharmacology, University of Gothenburg, Sweden; Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, University of Gothenburg, Sweden.
Institute of Neuroscience and Physiology, Department of Pharmacology, University of Gothenburg, Sweden.
Psychoneuroendocrinology. 2016 Jun;68:1-5. doi: 10.1016/j.psyneuen.2016.02.020. Epub 2016 Feb 23.
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.
自闭症谱系障碍(ASD)在男孩中比在女孩中更为普遍,这表明早期发育期间的高睾酮水平可能是一个风险因素。这一假设的证据来自于一些研究,这些研究显示胎儿睾酮水平以及产前雄激素化的间接测量指标与ASD和自闭症样特征(ALT)之间存在关联。在最近的一项研究中,我们报告了在瑞典儿童和青少年双胞胎研究(CATSS)的一个子集(n = 1771)中,ALT与编码雌激素受体1(ESR1)、2型类固醇5-α-还原酶(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。本研究的目的是试图在来自CATSS的另外一个更大的个体样本(n = 10,654)中重复这些发现,并分析SHBG和SRD5A2中其他具有功能重要性的SNP。在这个大的重复样本中,未发现ESR1和SRD5A2基因中先前相关的SNP与ALT之间存在关联。尽管如此,我们的结果表明,SHBG基因座上的两个非连锁SNP(rs6259和rs9901675)可能对男孩的语言障碍问题具有重要意义。本研究结果并未表明ESR1和SRD5A2基因中所研究的SNP在ALT中起主要作用,但不能排除SHBG基因变异可能产生的影响,尤其是对男孩语言障碍问题的影响。