C9orf72
失智症
突变
脑脊液
三核苷酸重复扩增
磷酸化
痴呆
内科学
生物
化学
病理
基因
遗传学
医学
疾病
等位基因
作者
Marc Suárez‐Calvet,Oriol Dols‐Icardo,Albert Lladó,Raquel Sánchez‐Valle,Isabel de la Torre Díez,G. Amer,Sofía Antón‐Aguirre,Daniel Alcolea,Juan Fortea,Irene Ferrer,Julie van der Zee,Lubina Dillen,Christine Van Broeckhoven,José Luís Molinuevo,Rafael Blesa,Jordi Clarimón,Alberto Lleó
标识
DOI:10.1136/jnnp-2013-305972
摘要
Objectives
About a half of patients with frontotemporal dementia (FTD) has deposition of phosphorylated TDP-43 protein (pTDP-43) in the brain. We studied pTDP-43 and total TDP-43 levels in plasma and cerebrospinal fluid (CSF) in healthy controls and patients with FTD, including those carrying a repeat expansion in the C9orf72 gene or a mutation in GRN. Methods
We included 88 plasma samples of 10 C9orf72 expansion carriers, 5 GRN mutation carriers, 51 patients with FTD without a known mutation and 22 healthy controls. We also obtained CSF samples from 25 patients with FTD (2 with C9orf72 expansion and 3 with a GRN mutation) and 22 healthy controls. We measured pTDP-43 and total TDP-43 levels using sandwich ELISA. Results
Patients carrying the C9orf72 repeat expansion or a GRN mutation had significantly higher plasma and CSF levels of pTDP-43 than the remaining patients with FTD (p<0.05). In addition, plasma pTDP-43 levels were higher in patients with FTD carrying a C9orf72 expansion or GRN mutations than in healthy controls (p<0.05). Conclusions
Our study shows that plasma pTDP-43 levels may be increased in some genetic forms of FTD known to be associated with TDP-43 proteinopathies.
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