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C9orf72重复序列扩增仅限于肌萎缩侧索硬化症-额颞叶痴呆谱系。

C9orf72 repeat expansions are restricted to the ALS-FTD spectrum.

作者信息

Ticozzi Nicola, Tiloca Cinzia, Calini Daniela, Gagliardi Stella, Altieri Alessandra, Colombrita Claudia, Cereda Cristina, Ratti Antonia, Pezzoli Gianni, Borroni Barbara, Goldwurm Stefano, Padovani Alessandro, Silani Vincenzo

机构信息

Department of Neurology and Laboratory of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Auxologico Italiano, Milan, Italy; Department of Pathophysiology and Transplantation, Dino Ferrari Center, Università degli Studi di Milano, Milan, Italy.

Department of Neurology and Laboratory of Neuroscience, Istituto di Ricovero e Cura a Carattere Scientifico Istituto Auxologico Italiano, Milan, Italy; Doctoral School in Molecular Medicine, Department of Sciences and Biomedical Technologies, University of Milan, Milan, Italy.

出版信息

Neurobiol Aging. 2014 Apr;35(4):936.e13-7. doi: 10.1016/j.neurobiolaging.2013.09.037. Epub 2013 Oct 2.

Abstract

Expansion of a GGGGCC repeat (RE) in the C9orf72 gene has been recently reported as the main genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Given the growing evidence of genetic and clinicopathologic overlap among ALS, FTD, and other neurodegenerative diseases, we investigated the occurrence of RE in a subset of 9 patients with ALS-plus syndromes, including Parkinson's disease (PD), progressive supranuclear palsy (PSP), corticobasal syndrome (CBS), and multiple system atrophy. We identified RE in 2 ALS-plus individuals (22.2%) displaying PSP and CBS features. On the basis of this finding, we extended our analysis to a cohort composed of 190 PD, 103 CBS, 107 PSP, and 177 Alzheimer's disease cases. We did not identify any RE in these patients, indicating that C9orf72 is in all probability not involved in the pathogenesis of these disorders. However, the high frequency of C9orf72 RE in patients with ALS-plus syndromes suggests that, similar to ALS-FTD patients, individuals with combined motor neuron and extrapyramidal features should be screened for RE, independent of their family history.

摘要

最近有报道称,C9orf72基因中GGGGCC重复序列(RE)的扩增是肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD)的主要遗传病因。鉴于越来越多的证据表明ALS、FTD和其他神经退行性疾病之间存在遗传和临床病理重叠,我们对9例患有ALS加综合征的患者进行了RE检测,这些综合征包括帕金森病(PD)、进行性核上性麻痹(PSP)、皮质基底节综合征(CBS)和多系统萎缩。我们在2例表现出PSP和CBS特征的ALS加综合征个体(22.2%)中发现了RE。基于这一发现,我们将分析扩展到一个由190例PD、103例CBS、107例PSP和177例阿尔茨海默病病例组成的队列。我们在这些患者中未发现任何RE,这表明C9orf72很可能不参与这些疾病的发病机制。然而,ALS加综合征患者中C9orf72 RE的高频率表明,与ALS-FTD患者类似,对于具有运动神经元和锥体外系特征组合的个体,无论其家族史如何,都应进行RE筛查。

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