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血清素转运体启动子变体:在印度自闭症患者及对照人群中的分析

Serotonin transporter promoter variants: Analysis in Indian autistic and control population.

作者信息

Guhathakurta Subhrangshu, Ghosh Sagarmoy, Sinha Swagata, Chatterjee Anindita, Ahmed Shabina, Chowdhury Susanta Roy, Gangopadhyay Prasanta Kumar, Ghosh Saurabh, Singh Manoranjan, Usha Rajamma

机构信息

Manovikas Biomedical Research and Diagnostic Centre, 482 Madudah, Plot I-24, Sector-J, EM Bypass, Kolkata 700 107, India.

出版信息

Brain Res. 2006 May 30;1092(1):28-35. doi: 10.1016/j.brainres.2006.03.078. Epub 2006 May 3.

Abstract

Serotonin transporter (5-HTT) is a transmembrane protein belonging to Na+/Cl- dependent membrane transporter family and transports 5-HT across the membranes of presynaptic neurons. 5-HTT-linked polymorphic region (5-HTTLPR) gained much interest because of the differential regulation of expression and activity of 5-HTT by its various genotypes. A population-based study has been conducted on 5-HTTLPR with 358 individuals, which included 79 autistic probands, 136 parents, and 143 controls from two subpopulations of east and northeast regions of India. The genotypic frequencies of all the groups conform to Hardy-Weinberg equilibrium. With the finding of efficacy of serotonin reuptake inhibitors in ameliorating ritualistic behavior in autistic disorder, 5-HTT emerged as a putative candidate gene for autism and association studies have been carried out in different ethnic populations. But these studies were inconclusive due to conflicting results on association. Because such a study has never been performed in the Indian population, we have tested the possible involvement of 5-HTTLPR polymorphism with autism. The present study failed to establish any association or linkage of 5-HTTLPR with autism in the Indian population by case-control studies (chi2 = 1.314, P = 0.63) and family-based approaches (TDT chi2 = 0.22, P = 0.64 and HHRR-chi2 = 0.25, P = 0.61). However, when a meta-analysis of all the available TDT data, inclusive of the present study is carried out, we observed a significant preferential transmission of S-allele from parents to the affected offspring (chi2 = 7.51, P = 0.006) indicating an association of 5-HTTLPR with autism.

摘要

血清素转运体(5-HTT)是一种跨膜蛋白,属于Na+/Cl-依赖性膜转运体家族,可将5-羟色胺转运过突触前神经元的膜。5-HTT连锁多态性区域(5-HTTLPR)因其不同基因型对5-HTT表达和活性的差异调节而备受关注。对358名个体进行了一项基于人群的5-HTTLPR研究,其中包括来自印度东部和东北部两个亚群体的79名自闭症先证者、136名父母和143名对照。所有组的基因型频率均符合哈迪-温伯格平衡。随着血清素再摄取抑制剂在改善自闭症仪式行为方面疗效的发现,5-HTT成为自闭症的一个假定候选基因,并已在不同种族人群中进行了关联研究。但由于关联结果相互矛盾,这些研究尚无定论。因为在印度人群中从未进行过此类研究,所以我们测试了5-HTTLPR多态性与自闭症的可能关联。本研究通过病例对照研究(卡方=1.314,P=0.63)和基于家系的方法(传递不平衡检验卡方=0.22,P=0.64和家系相对风险比卡方=0.25,P=0.61)未能在印度人群中确定5-HTTLPR与自闭症的任何关联或连锁关系。然而,当对所有可用的传递不平衡检验数据(包括本研究)进行荟萃分析时,我们观察到S等位基因从父母向受影响后代的显著优先传递(卡方=7.51,P=0.006),表明5-HTTLPR与自闭症有关联。

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