痴呆
失智症
肌萎缩侧索硬化
C9orf72
疾病
认知
医学
额颞叶变性
神经退行性变
共济失调
路易氏体型失智症
快速眼动睡眠行为障碍
认知功能衰退
病理
心理学
帕金森病
精神科
作者
Anita Korpioja,Johanna Krüger,Anri Hurme‐Niiranen,Eino Solje,Kasper Katisko,Joonas Lipponen,Maria Lehtilahti,Anne M. Remes,Kari Majamaa,Laura Kytövuori
标识
DOI:10.1016/j.parkreldis.2022.08.034
摘要
Abstract
Introduction
The biallelic repeat expansion (AAGGG)exp in RFC1 causes cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS). Recently, cognitive impairment has been reported in patients with CANVAS and a broader neurodegenerative process associated with RFC1 has been suggested. Furthermore, rare cases of multiple system atrophy, Parkinson's disease, amyotrophic lateral sclerosis or CANVAS with features of dementia with Lewy bodies have been found. Objective
We hypothesized that the biallelic (AAGGG)exp is associated with neurodegeneration manifested as cognitive symptoms and that atypical RFC1 disease may be found among patients with cognitive disorder. Methods
Clinical data on nine patients with biallelic (AAGGG)exp were reviewed and 564 patients with Alzheimer's disease or frontotemporal dementia (FTD) were investigated for biallelic RFC1 (AAGGG)exp. Results
Five patients with biallelic (AAGGG)exp were found with a cognitive impairment and in four of them the phenotype resembled FTD. However, biallelic (AAGGG)exp was not detected among patients with Alzheimer's disease or FTD. Conclusion
Cognitive impairment is a feature in patients with the biallelic (AAGGG)exp, but the pathogenic expansion seems to be rare in patients with dementia. Studies on patients with diverse phenotypes would be useful to further explore the involvement of RFC1 in neuronal degeneration and to identify atypical phenotypes, which should be taken into account in clinical practice.
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