Koishi Shinko, Yamamoto Kenji, Matsumoto Hideo, Koishi Seiji, Enseki Youichi, Oya Akitoshi, Asakura Arata, Aoki Yutaka, Atsumi Mariko, Iga Tomiei, Inomata Jyoji, Inoko Hidetoshi, Sasaki Tsukasa, Nanba Eiji, Kato Nobumasa, Ishii Tetsuo, Yamazaki Kosuke
Department of Psychiatry, Course of Specialized Clinical Science, Tokai University School of Medicine, Bohseidai, Isehara, Kanagawa 259-1193, Japan.
Brain Dev. 2006 May;28(4):257-60. doi: 10.1016/j.braindev.2005.09.003. Epub 2006 Feb 14.
Autism is now widely accepted as a biological disorder which, by and large, starts before birth. It has been shown that serotonin (5-HT) is associated with several psychological processes and hyperserotoninemia is observed in some autistic patients. The results of previous reports about family-based association studies between the serotonin transporter (5-HTT) gene promoter polymorphism and autism are controversial. In this study, an analysis using the transmission/disequilibrium test (TDT) between the 5-HTT gene promoter polymorphism and autism in 104 trios, all ethnically Japanese, showed no significant linkage disequilibrium (P=0.17). Recently, it has been reported that some haplotypes at the serotonin transporter locus may be associated with the pathogenesis of autism. Therefore, further investigations by haplotype analyses are necessary to confirm the implications of genetic variants of the serotonin transporter in the etiology of autism.
自闭症目前已被广泛认为是一种主要在出生前就开始的生物紊乱疾病。研究表明,血清素(5-羟色胺,5-HT)与多种心理过程相关,并且在一些自闭症患者中观察到血清素水平过高。先前关于血清素转运体(5-HTT)基因启动子多态性与自闭症之间基于家系的关联研究结果存在争议。在本研究中,对104个均为日本种族的三联体进行了5-HTT基因启动子多态性与自闭症之间的传递不平衡检验(TDT)分析,结果显示无显著连锁不平衡(P = 0.17)。最近,有报道称血清素转运体位点的某些单倍型可能与自闭症的发病机制有关。因此,有必要通过单倍型分析进行进一步研究,以证实血清素转运体基因变异在自闭症病因学中的意义。