Literature DB >> 31914226

Comparison of sporadic and familial behavioral variant frontotemporal dementia (FTD) in a North American cohort.

Hilary W Heuer1, P Wang1, K Rascovsky2, A Wolf1, B Appleby3, J Bove2, Y Bordelon4, P Brannelly5, D E Brushaber6, C Caso7, G Coppola4, B Dickerson8, S Dickinson9, K Domoto-Reilly7, K Faber10, J Ferrall11, J Fields6, A Fishman12, J Fong1, T Foroud10, L K Forsberg6, D Gearhart6, B Ghazanfari13, N Ghoshal14, J Goldman15, J Graff-Radford6, N Graff-Radford16, I Grant17, M Grossman2, D Haley16, G-Y Hsiung18, E Huey15, D Irwin2, D Jones6, K Kantarci6, A Karydas1, D Kaufer11, D Kerwin19, D Knopman6, J Kornak1, J H Kramer1, R Kraft6, W K Kremers6, W Kukull20, I Litvan21, P Ljubenkov1, I R Mackenzie18, M Maldonado4, M Manoochehri15, S McGinnis8, E McKinley22, M F Mendez4, B L Miller1, C Onyike12, A Pantelyat12, R Pearlman23, L Petrucelli16, M Potter10, R Rademakers16, E M Ramos4, K P Rankin1, E D Roberson22, E Rogalski17, P Sengdy18, L Shaw2, J Syrjanen6, M C Tartaglia13, N Tatton9, J Taylor1, A Toga24, J Trojanowski3, S Weintraub17, B Wong8, Z Wszolek16, B F Boeve6, H J Rosen1, A L Boxer1.   

Abstract

INTRODUCTION: Behavioral variant frontotemporal dementia (bvFTD) may present sporadically or due to an autosomal dominant mutation. Characterization of both forms will improve understanding of the generalizability of assessments and treatments.
METHODS: A total of 135 sporadic (s-bvFTD; mean age 63.3 years; 34% female) and 99 familial (f-bvFTD; mean age 59.9; 48% female) bvFTD participants were identified. f-bvFTD cases included 43 with known or presumed chromosome 9 open reading frame 72 (C9orf72) gene expansions, 28 with known or presumed microtubule-associated protein tau (MAPT) mutations, 14 with known progranulin (GRN) mutations, and 14 with a strong family history of FTD but no identified mutation.
RESULTS: Participants with f-bvFTD were younger and had earlier age at onset. s-bvFTD had higher total Neuropsychiatric Inventory Questionnaire (NPI-Q) scores due to more frequent endorsement of depression and irritability. DISCUSSION: f-bvFTD and s-bvFTD cases are clinically similar, suggesting the generalizability of novel biomarkers, therapies, and clinical tools developed in either form to the other.
© 2020 the Alzheimer's Association.

Entities:  

Keywords:  C9orf72; GRN; MAPT; bvFTD; clinical trials; frontotemporal dementia; genetics

Mesh:

Substances:

Year:  2020        PMID: 31914226      PMCID: PMC7192555          DOI: 10.1002/alz.12046

Source DB:  PubMed          Journal:  Alzheimers Dement        ISSN: 1552-5260            Impact factor:   21.566


  23 in total

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