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5-羟色胺转运体基因启动子区多态性(5-HTTLPR)及环境危险因素对巴西自闭症谱系障碍患者样本的影响。

Influence of the 5-HTTLPR polymorphism and environmental risk factors in a Brazilian sample of patients with autism spectrum disorders.

作者信息

Longo Dânae, Schüler-Faccini Lavínia, Brandalize Ana Paula Carneiro, dos Santos Riesgo Rudimar, Bau Claiton Henrique Dotto

机构信息

Graduate Program in Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul, Brazil.

出版信息

Brain Res. 2009 Apr 24;1267:9-17. doi: 10.1016/j.brainres.2009.02.072. Epub 2009 Mar 10.

Abstract

The 5-HTTLPR polymorphism of serotonin transporter gene is widely investigated in association studies in autism spectrum disorders (ASD). The results of such studies, however, remain controversial possibly due to the great genetic heterogeneity related to ASD and the lack of evaluation of the triallelic functional structure of 5-HTTLPR. This study tested for association between the 5-HTTLPR and ASD in a Brazilian sample by case-control and family-based association test (FBAT) methods, considering the biallelic and triallelic structures of this polymorphism. In addition, we performed an exploratory analysis of associations between specific clinical outcomes of ASD patients and 5-HTTLPR as well as several prenatal environmental factors. Genotyping was achieved in 151 ASD patients, 179 unrelated controls and 105 complete trios. There was no evidence of association between the 5-HTTLPR with ASD in both case-control and FBAT tests, but the LaLa 5-HTTLPR genotype was associated with mood instability in patients (P=0.006). The prenatal exposure to potential neuroteratogenic drugs was associated with epilepsy (P<0.001). Our findings suggest that the 5-HTTLPR is not associated with ASD in the Brazilian population, even considering the triallelic structure. Additionally, this study suggested a role of the 5-HTTLPR and environmental factors in the clinical expression of ASD.

摘要

血清素转运体基因的5-HTTLPR多态性在自闭症谱系障碍(ASD)的关联研究中得到了广泛调查。然而,此类研究的结果仍存在争议,这可能是由于与ASD相关的巨大遗传异质性以及对5-HTTLPR三等位基因功能结构缺乏评估所致。本研究通过病例对照和基于家系的关联测试(FBAT)方法,在一个巴西样本中测试了5-HTTLPR与ASD之间的关联,同时考虑了该多态性的双等位基因和三等位基因结构。此外,我们还对ASD患者的特定临床结局与5-HTTLPR以及几种产前环境因素之间的关联进行了探索性分析。对151例ASD患者、179名无关对照和105个完整三联体进行了基因分型。在病例对照和FBAT测试中,均未发现5-HTTLPR与ASD之间存在关联的证据,但LaLa 5-HTTLPR基因型与患者的情绪不稳定有关(P=0.006)。产前接触潜在的神经致畸药物与癫痫有关(P<0.001)。我们的研究结果表明,即使考虑三等位基因结构,5-HTTLPR在巴西人群中也与ASD无关。此外,本研究表明5-HTTLPR和环境因素在ASD的临床表型中发挥作用。

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