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tau基因多态性与帕金森病发病年龄的相关性。

Correlation of tau gene polymorphism with age at onset of Parkinson's disease.

作者信息

Kobayashi Hideaki, Ujike Hiroshi, Hasegawa Junko, Yamamoto Mitsutoshi, Kanzaki Akihiro, Sora Ichiro

机构信息

Department of Psychobiology, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai 980-8574, Japan.

出版信息

Neurosci Lett. 2006 Sep 25;405(3):202-6. doi: 10.1016/j.neulet.2006.06.057. Epub 2006 Jul 28.

Abstract

Parkinson's disease (PD) is a neurodegenerative disease and its prevalence increases with age. The microtubule-associated protein tau (MAPT) is thought to be implicated in the pathogenesis of PD. Association of the MAPT H1 haplotype with PD in Caucasians has been extensively studied, however, the results were inconsistent. In this study, we investigated whether MAPT gene variants contribute to the pathogenesis process including the age at onset in Japanese PD. Promoter region of MAPT gene was analyzed to find polymorphisms in Japanese population. Two single nucleotide polymorphisms (SNPs), C-639T and Del-568TIns, in promoter region were found. C-639T was novel. Unlike Caucasians, the -226C and -45A alleles consisting of the H1 haplotype were monomorphic in Japanese population. Association analysis was performed using 240 PD and 191 controls in these SNPs. No significant association was observed between these SNPs and PD. Haplotype analysis also showed no significant association (P=0.72). However, the age at onset showed significant correlation with the genotypes of Del-568TIns in PD samples when analyzed by Kendall rank correlation test (Kendall tau=-0.098, P=0.0243). These results suggested that MAPT gene variants may modify the pathogenesis process of PD.

摘要

帕金森病(PD)是一种神经退行性疾病,其患病率随年龄增长而增加。微管相关蛋白tau(MAPT)被认为与PD的发病机制有关。MAPT H1单倍型与白种人PD的关联已得到广泛研究,然而,结果并不一致。在本研究中,我们调查了MAPT基因变异是否参与了日本PD患者发病机制过程,包括发病年龄。对MAPT基因的启动子区域进行分析,以寻找日本人群中的多态性。在启动子区域发现了两个单核苷酸多态性(SNP),即C-639T和Del-568TIns。C-639T是新发现的。与白种人不同,组成H1单倍型的-226C和-45A等位基因在日本人群中是单态的。在这些SNP中,对240例PD患者和191例对照进行了关联分析。未观察到这些SNP与PD之间存在显著关联。单倍型分析也未显示出显著关联(P=0.72)。然而,通过肯德尔等级相关检验分析时,PD样本的发病年龄与Del-568TIns的基因型显示出显著相关性(肯德尔tau=-0.098,P=0.0243)。这些结果表明,MAPT基因变异可能会改变PD的发病机制过程。

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