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血清素转运体基因多态性与轻度阿尔茨海默病中的行为和心理症状

Serotonin transporter gene polymorphism and BPSD in mild Alzheimer's disease.

作者信息

Ueki Akinori, Ueno Hideo, Sato Noriko, Shinjo Hidetaka, Morita Yoshio

机构信息

Department of Neuropsychiatry, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.

出版信息

J Alzheimers Dis. 2007 Nov;12(3):245-53. doi: 10.3233/jad-2007-12306.

Abstract

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.

摘要

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。

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