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Genetic study of young‐onset dementia using targeted gene panel sequencing in Taiwan
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ( IF 2.8 ) Pub Date : 2021-02-13 , DOI: 10.1002/ajmg.b.32836 Jung‐Lung Hsu, Chin‐Hsien Lin, Pei‐Lung Chen, Kun‐Ju Lin, Ta‐Fu Chen
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ( IF 2.8 ) Pub Date : 2021-02-13 , DOI: 10.1002/ajmg.b.32836 Jung‐Lung Hsu, Chin‐Hsien Lin, Pei‐Lung Chen, Kun‐Ju Lin, Ta‐Fu Chen
Recent genetic progress allows the molecular diagnosis of young‐onset dementia, including Alzheimer's disease (AD) and frontotemporal dementia (FTD). We aimed to identify the mutational and clinical spectra of causal genes in a Taiwanese cohort of young‐onset dementia. Ninety‐one patients with young‐onset dementia and 22 age/gender‐matched controls were recruited. Genetic causes were identified by a targeted panel containing 90 causative genes for AD, FTD, and related neurodegenerative disorders. Plasma biomarkers, including total tau, Aβ42, and Aβ40, were assayed. Molecular amyloid and tau PET scans were performed in some patients carrying mutations. Nine of 52 patients (17.3%) with young‐onset AD had mutations: 2 (22.2%), 4 (44.5%), 2 (22.2%), and 1 (11.1%) in APP, PSEN1, PSEN2, and TREM2, respectively. Two of 33 patients (6.1%) with young‐onset FTD had mutations in MAPT and LRRK2. Three of the 6 patients (50.0%) with possible FTD combined with other neurodegenerative disorders had individual mutations in APP, PSEN2, or MAPT. Patients with PSEN1 mutations had earlier onset of disease than those without mutations (p = .02). Plasma level of total tau was increased and Aβ42 and Aβ40 levels decreased in all groups of dementia patients compared to controls. Our findings provide a genetic spectrum of young‐onset dementia in our population.
更新日期：2021-03-10
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