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与色氨酸羟化酶 2 基因多态性与韩国家族性自闭症谱系障碍的关联。

Association with tryptophan hydroxylase 2 gene polymorphisms and autism spectrum disorders in Korean families.

机构信息

Department of Pharmacology, School of Medicine, Eulji University, 77, Gyeryong-ro, 771 Beon-gil, Jung-gu, Daejeon 301-746, Republic of Korea.

出版信息

Neurosci Res. 2012 Aug;73(4):333-6. doi: 10.1016/j.neures.2012.05.012. Epub 2012 Jun 12.

Abstract

It was performed a family-based association study of 6 single nucleotide polymorphisms (SNPs) from the TPH2 with autism spectrum disorder (ASD) in 151 Korean trios. We found a significant association at the rs2129575 with ASD susceptibility (corrected p=0.006). Furthermore, after conducting with the quantitative scores in the Autism Diagnostic Interview-Revised, there were associations between restricted, repetitive, and stereotyped patterns of behavior (preoccupation with parts of objects or nonfunctional elements of materials) in ASD and SNPs in TPH2. These results suggest that TPH2 polymorphisms influence the phenotypic impairments of ASD and enhance ASD susceptibility.

摘要

进行了一项基于家系的关联研究,共涉及 151 个韩国家系中的 6 个色氨酸羟化酶 2(TPH2)单核苷酸多态性(SNPs)与自闭症谱系障碍(ASD)的相关性。我们发现 rs2129575 与 ASD 易感性显著相关(校正后 p=0.006)。此外,在对自闭症诊断访谈修订版的定量评分进行分析后,发现 TPH2 中的 SNPs 与 ASD 患者的受限、重复和刻板行为模式(对物体的部分或材料的非功能元素的过分关注)之间存在关联。这些结果表明,TPH2 多态性影响 ASD 的表型损伤,并增加 ASD 的易感性。

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