| Literature DB >> 29226866 |
Liyong Wu1,2, Jia Liu1, Xueyan Feng1, Jing Dong1, Wei Qin1, Yang Liu1, Jingjuan Wang3, Jie Lu3,4, Kewei Chen5, Yuping Wang1, Jianping Jia1.
Abstract
Frontotemporal dementia with parkinsonism-linked to chromosome 17 (FTDP-17) is a rare autosomal dominant neurodegenerative disorder. Most patients with FTDP-17 carry the mutation in the microtubule-associated protein tau (MAPT) gene. Striatum is predominantly and early affected in FTDP-17. Five family members (two symptomatic patients and three presymptomatic mutation carriers) from a Chinese pedigree of FTDP-17 with N279K mutation in MAPT were enrolled. Parkinsonism was the initial symptom for symptomatic patients. 2b-carbomethoxy-3b-(4-trimethylstannylphenyl) tropane (11C-CFT) uptake was obviously affected in the putamen of two presymptomatic mutation carriers. Presymptomatic case 3, whose 11C-CFT uptake in the right putamen was normal at baseline, was still free of parkinsonism during follow-up. In conclusion, 11C-CFT-positron emission tomography could be a potential biomarker for the presymptomatic stage of FTDP-17 to predict the disease onset.Entities:
Keywords: 11C-CFT-PET; frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17); microtubule-associated protein tau (MAPT); presymptomatic mutation carriers
Mesh:
Substances:
Year: 2018 PMID: 29226866 DOI: 10.3233/JAD-170561
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472