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该基因中的GGC重复序列扩增与以运动感觉和自主神经病变为主的表型相关。

GGC Repeat Expansion in the Gene Is Associated With a Phenotype of Predominant Motor-Sensory and Autonomic Neuropathy.

作者信息

Wang Hui, Yu Jiaxi, Yu Meng, Deng Jianwen, Zhang Wei, Lv He, Liu Jing, Shi Xin, Liang Wei, Jia Zhirong, Hong Daojun, Meng Lingchao, Wang Zhaoxia, Yuan Yun

机构信息

Department of Neurology, Peking University First Hospital, Beijing, China.

Beijing Key Laboratory of Neurovascular Disease Discovery, Beijing, China.

出版信息

Front Genet. 2021 Jul 7;12:694790. doi: 10.3389/fgene.2021.694790. eCollection 2021.

Abstract

There is still a considerable proportion of patients with inherited peripheral neuropathy (IPN) whose pathogenic genes are unknown. This study was intended to investigate whether the GGC repeat expansion in the is presented in some patients with IPN. A total of 142 unrelated mainland Chinese patients with highly suspected diagnosis of IPN without any known causative gene were recruited. Repeat-primed polymerase chain reaction (RP-PCR) was performed to screen GGC repeat expansion in , followed by fluorescence amplicon length analysis-PCR (AL-PCR) to determine the GGC repeat size. Detailed clinical data as well as nerve, muscle, and skin biopsy were reviewed and analyzed in the -related IPN patients. In total, five of the 142 patients (3.52%) were found to have pathogenic GGC expansion in , with repeat size ranging from 126 to 206 repeats. All the -related IPN patients presented with adult-onset motor-sensory and autonomic neuropathy that predominantly affected the motor component of peripheral nerves. While tremor and irritating dry cough were noted in four-fifths of the patients, no other signs of the central nervous system were presented. Electrophysiological studies revealed both demyelinating and axonal changes of polyneuropathy that were more severe in lower limbs and asymmetrically in upper limbs. Sural nerve pathology was characterized by multiple fibers with thin myelination, indicating a predominant demyelinating process. Muscle pathology was consistent with neuropathic changes. P62-positive intranuclear inclusions were observed in nerve, skin, and muscle tissues. Our study has demonstrated that GGC expansion in is associated with IPN presenting as predominant motor-sensory and autonomic neuropathy, which expands the phenotype of the -related repeat expansion spectrum. Screening of GGC repeat expansions in the should be considered in patients presenting with peripheral neuropathy with tremor and irritating dry cough.

摘要

仍有相当比例的遗传性周围神经病(IPN)患者的致病基因未知。本研究旨在调查某些IPN患者中是否存在[具体基因名称]的GGC重复扩增。共招募了142名来自中国大陆的无亲缘关系且高度疑似诊断为IPN但无任何已知致病基因的患者。采用重复引物聚合酶链反应(RP-PCR)筛选[具体基因名称]中的GGC重复扩增,随后进行荧光扩增片段长度分析-PCR(AL-PCR)以确定GGC重复大小。对与[具体基因名称]相关的IPN患者的详细临床数据以及神经、肌肉和皮肤活检进行了回顾和分析。总共142名患者中有5名(3.52%)被发现存在[具体基因名称]的致病性GGC扩增,重复大小范围为126至206次重复。所有与[具体基因名称]相关的IPN患者均表现为成人起病的运动感觉和自主神经病变,主要影响周围神经的运动成分。五分之四的患者出现震颤和刺激性干咳,但未出现中枢神经系统的其他体征。电生理研究显示多神经病的脱髓鞘和轴索改变,下肢更为严重,上肢不对称。腓肠神经病理学特征为多条纤维髓鞘薄,表明主要为脱髓鞘过程。肌肉病理学与神经病变一致。在神经、皮肤和肌肉组织中观察到p62阳性核内包涵体。我们的研究表明,[具体基因名称]中的GGC扩增与以主要运动感觉和自主神经病变为表现的IPN相关,这扩展了与[具体基因名称]相关的重复扩增谱的表型。对于表现为周围神经病并伴有震颤和刺激性干咳的患者,应考虑筛查[具体基因名称]中的GGC重复扩增。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aca/8293674/1e023f520073/fgene-12-694790-g001.jpg

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