Neuroimaging in genetic frontotemporal dementia and amyotrophic lateral sclerosis
Author(s) -
Suvi Häkkinen,
Stephanie A. Chu,
Suzee E. Lee
Publication year - 2020
Publication title -
neurobiology of disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.205
H-Index - 166
eISSN - 1095-953X
pISSN - 0969-9961
DOI - 10.1016/j.nbd.2020.105063
Subject(s) - c9orf72 , frontotemporal dementia , amyotrophic lateral sclerosis , tardbp , neuroimaging , neuroscience , sod1 , psychology , dementia , medicine , pathology , disease
Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) have a strong clinical, genetic and pathological overlap. This review focuses on the current understanding of structural, functional and molecular neuroimaging signatures of genetic FTD and ALS. We overview quantitative neuroimaging studies on the most common genes associated with FTD (MAPT, GRN), ALS (SOD1), and both (C9orf72), and summarize visual observations of images reported in the rarer genes (CHMP2B, TARDBP, FUS, OPTN, VCP, UBQLN2, SQSTM1, TREM2, CHCHD10, TBK1).
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