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DYT1基因突变的显性和隐性携带者中不同模式的电生理缺陷

Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation.

作者信息

Edwards Mark J, Huang Ying-Zu, Wood Nicholas W, Rothwell John C, Bhatia Kailash P

机构信息

Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.

出版信息

Brain. 2003 Sep;126(Pt 9):2074-80. doi: 10.1093/brain/awg209. Epub 2003 Jun 23.

Abstract

A mutation in the DYT1 gene on chromosome 9q34 causes early-onset primary torsion dystonia with autosomal dominant inheritance but low phenotypic penetrance. The aim of the present study was to assess the functional consequences of the DYT1 gene, by comparing the electrophysiology of cortical and spinal circuits in clinically affected and unaffected carriers of the DYT1 gene mutation. We assessed intracortical inhibition (ICI), intracortical facilitation (ICF), the cortical silent period (SP) and spinal reciprocal inhibition (RI) in 10 manifesting DYT1 gene carriers (MDYT1), seven non-manifesting DYT1 gene carriers (NMDYT1) and 13 healthy controls. The MDYT1 subjects had abnormalities similar to those seen in previous studies of non-genetically characterized individuals with primary dystonia. They had reduced ICI, shorter SP and absent presynaptic phase of RI compared with the healthy controls. NMDYT1 subjects also had a significant reduction in cortical inhibition (ICI and SP), but their spinal RI was not different from controls. We conclude that clinical expression of dystonia depends on widespread electrophysiological deficits, and the presence of the DYT1 gene mutation itself leads only to a subset of these changes. This is consistent with the hypothesis that additional environmental/genetic insults may be needed to reveal clinical symptoms in DYT1 gene carriers.

摘要

9号染色体长臂34区(9q34)上DYT1基因的突变会导致早发性原发性扭转性肌张力障碍,呈常染色体显性遗传,但表型外显率较低。本研究的目的是通过比较DYT1基因突变的临床受累携带者和未受累携带者皮质及脊髓回路的电生理,来评估DYT1基因的功能后果。我们评估了10名有症状的DYT1基因携带者(MDYT1)、7名无症状的DYT1基因携带者(NMDYT1)和13名健康对照者的皮质内抑制(ICI)、皮质内易化(ICF)、皮质静息期(SP)和脊髓交互抑制(RI)。MDYT1受试者存在与先前对非基因特征性原发性肌张力障碍个体研究中所见相似的异常。与健康对照者相比,他们的ICI降低、SP缩短且RI的突触前相缺失。NMDYT1受试者的皮质抑制(ICI和SP)也显著降低,但其脊髓RI与对照者无差异。我们得出结论,肌张力障碍的临床表型取决于广泛的电生理缺陷,DYT1基因突变本身仅导致这些变化的一部分。这与以下假设一致,即可能需要额外的环境/基因损伤才能使DYT1基因携带者出现临床症状。

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