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中国肌萎缩侧索硬化症患者中VCP突变的表型

Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients.

作者信息

Feng Shu-Yan, Lin Han, Che Chun-Hui, Huang Hua-Pin, Liu Chang-Yun, Zou Zhang-Yu

机构信息

Department of Neurophysiology, Henan Provincial People's Hospital, Zhengzhou, China.

Zhengzhou University People's Hospital, Zhengzhou, China.

出版信息

Front Neurol. 2022 Feb 7;13:790082. doi: 10.3389/fneur.2022.790082. eCollection 2022.

DOI:10.3389/fneur.2022.790082
PMID:35197922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8858817/
Abstract

Mutations in the valosin-containing protein (VCP) gene have been linked to amyotrophic lateral sclerosis (ALS) in the Caucasian populations. However, the phenotype of VCP mutations in Chinese patients with (ALS) remains unclear. Targeted next-generation sequencing covered 28 ALS-related genes including the VCP gene was undertaken to screen in a Chinese cohort of 275 sporadic ALS cases and 15 familial ALS pedigrees. An extensive literature review was performed to identify all patients with ALS carrying VCP mutations previously reported. The clinical characteristics and genetic features of ALS patients with VCP mutations were reviewed. One known p.R155C mutation in the VCP gene was detected in two siblings from a familial ALS pedigree and two sporadic individuals. In addition, the same VCP p.R155C mutation was detected in an additional patient with ALS referred in 2021. Three patients with VCP p.R155C mutation presented with muscular weakness starting from proximal extremities to distal extremities. The other patient developed a phenotype of Paget's disease of bone in addition to the progressive muscular atrophy. We reported the first VCP mutation carrier manifesting ALS with Paget's disease of bone in the Chinese population. Our findings expand the phenotypic spectrum of the VCP mutations in Chinese patients with ALS and suggest that ALS patients with VCP p.R155C mutations tend to present with relatively young onset, symmetrical involvement of proximal muscles weakness of arms or legs, and then progressed to distal muscles of limbs.

摘要

含缬酪肽蛋白(VCP)基因突变与白种人群的肌萎缩侧索硬化症(ALS)相关。然而,中国ALS患者中VCP基因突变的表型仍不清楚。我们对275例散发型ALS病例和15个家族性ALS家系的中国队列进行了靶向二代测序,覆盖包括VCP基因在内的28个与ALS相关的基因。我们进行了广泛的文献综述,以确定所有先前报道的携带VCP基因突变的ALS患者。我们对携带VCP基因突变的ALS患者的临床特征和遗传特征进行了综述。在一个家族性ALS家系的两名同胞和两名散发病例中检测到VCP基因中一个已知的p.R155C突变。此外,在2021年转诊的另一名ALS患者中也检测到相同的VCP p.R155C突变。三名携带VCP p.R155C突变的患者表现为从近端肢体到远端肢体的肌肉无力。另一名患者除进行性肌肉萎缩外,还出现了骨佩吉特病的表型。我们报道了中国人群中首例表现为伴有骨佩吉特病的ALS的VCP突变携带者。我们的研究结果扩展了中国ALS患者中VCP基因突变的表型谱,并表明携带VCP p.R155C突变的ALS患者往往发病年龄相对较轻,手臂或腿部近端肌肉无力呈对称性受累,然后进展至四肢远端肌肉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4630/8858817/ed1a13665239/fneur-13-790082-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4630/8858817/ed1a13665239/fneur-13-790082-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4630/8858817/ed1a13665239/fneur-13-790082-g0001.jpg

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Brain. 2021 Aug 17;144(7):1985-1993. doi: 10.1093/brain/awab078.
2
Genetic epidemiology of familial ALS in Brazil.巴西家族性肌萎缩侧索硬化症的遗传流行病学。
Neurobiol Aging. 2021 Jun;102:227.e1-227.e4. doi: 10.1016/j.neurobiolaging.2021.01.007. Epub 2021 Jan 22.
3
Value of systematic genetic screening of patients with amyotrophic lateral sclerosis.
Brain Behav. 2024 Nov;14(11):e70115. doi: 10.1002/brb3.70115.
4
A pathogenic mutation in the ALS/FTD gene VCP induces mitochondrial hypermetabolism by modulating the permeability transition pore.ALS/FTD 基因 VCP 的致病性突变通过调节通透性转换孔诱导线粒体过度代谢。
Acta Neuropathol Commun. 2024 Oct 10;12(1):161. doi: 10.1186/s40478-024-01866-0.
5
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Mol Neurodegener. 2023 Aug 7;18(1):52. doi: 10.1186/s13024-023-00639-y.
6
Novel Variants in the Gene Causing Multisystem Proteinopathy 1.导致多系统蛋白病 1 的 基因中的新型变异。
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4
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J Med Genet. 2020 May 14. doi: 10.1136/jmedgenet-2020-106866.
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Eur J Neurol. 2020 Jun;27(6):1017-1022. doi: 10.1111/ene.14213. Epub 2020 Apr 10.