Ueki Akinori, Ueno Hideo, Sato Noriko, Shinjo Hidetaka, Morita Yoshio
Department of Neuropsychiatry, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
J Alzheimers Dis. 2007 Nov;12(3):245-53. doi: 10.3233/jad-2007-12306.
The purpose of the present study was to confirm an association of functional polymorphism within the serotonin transporter (5-HTT) gene with Alzheimer's disease (AD) and behavioral and psychological symptoms of dementia (BPSD) in mild AD. Apolipoprotein E (ApoE) gene polymorphism and 2 types of functional polymorphism in the 5-HTT gene, 5-HTT-linked polymorphic region (5-HTTLPR) and a 5-HTT variable number of tandem repeats sequence (5-HTTVNTR) were analyzed longitudinally in outpatients with mild AD to find out whether there was a relation between any such polymorphisms and the occurrence of BPSD. No significant differences in genotype distribution or allele frequencies were identified for 5-HTTLPR or 5-HTTVNTR between AD patients and age- and sex-matched non-demented controls regardless of ApoE epsilon4 allele. No significant differences were noted in 5-HTTLPR genotype or allele distributions between AD patients with or without BPSD. However, significant associations were observed between presence of 5-HTTVNTR allele 10 and BPSD or aggressiveness. This difference was independent of the presence of the ApoE epsilon4 allele. As a result, 5-HTT polymorphisms are unlikely to play any substantial role in susceptibility to AD. Conversely, 5-HTTVNTR influences the risk of developing BPSD or aggressiveness and genetic variations in the 5-HTT gene may be involved in the development of symptomatology for mild AD.
本研究的目的是证实血清素转运体(5-HTT)基因内的功能多态性与轻度阿尔茨海默病(AD)及痴呆的行为和心理症状(BPSD)之间的关联。对轻度AD门诊患者的载脂蛋白E(ApoE)基因多态性以及5-HTT基因中的两种功能多态性,即5-HTT连锁多态性区域(5-HTTLPR)和5-HTT可变串联重复序列(5-HTTVNTR)进行纵向分析,以查明这些多态性与BPSD的发生是否存在关联。无论ApoE ε4等位基因如何,AD患者与年龄和性别匹配的非痴呆对照在5-HTTLPR或5-HTTVNTR的基因型分布或等位基因频率上均未发现显著差异。有或无BPSD的AD患者在5-HTTLPR基因型或等位基因分布上未观察到显著差异。然而,观察到5-HTTVNTR等位基因10的存在与BPSD或攻击性之间存在显著关联。这种差异与ApoE ε4等位基因的存在无关。因此,5-HTT多态性不太可能在AD易感性中发挥任何实质性作用。相反,5-HTTVNTR影响发生BPSD或攻击性的风险,并且5-HTT基因的遗传变异可能参与轻度AD症状学的发展。