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Genetic marker for the diagnosis of dementia with lewy bodies

机译:诊断路易体痴呆的遗传标记

摘要

Specific polymorphisms in BChE gene have been found which allow determining whether a patient suffers from dementia with Lewy bodies (DLB), and allow distinguishing it from Alzheimer's disease. The invention provides an in vitro method for the diagnosis of DLB comprising determining in a biological sample from a subject, the genotype of the following polymorphisms in butyrylcholinesterase (BChE) gene: the polymorphic site at position 3687 in NCBI Accession Number NG_009031 (i.e. SEQ ID NO: 1 ) the polymorphic site at position 4206 in SEQ ID NO: 1, the polymorphic site at position 4443 in SEQ ID NO: 1. and the polymorphic site at position 68974 in NCBI Accession Number NG_009031 (i.e. position 934 in SEQ ID NO: 26).
机译:已经发现了BChE基因中的特定多态性,其可以确定患者是否患有路易体痴呆症(DLB),并且可以将其与阿尔茨海默氏病区分开。本发明提供了用于诊断DLB的体外方法,其包括在来自受试者的生物样品中确定丁酰胆碱酯酶(BChE)基因中以下多态性的基因型:NCBI登录号NG_009031中3687位的多态性位点(即SEQ ID NO: NO:1)SEQ ID NO:1中4206位的多态性位点,SEQ ID NO:1中4443位的多态性位点和NCBI登录号NG_009031中68974位的多态性位点(即SEQ ID NO:934中的934位) :26)。

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