TY - JOUR
T1 - Subcortical and deep cortical atrophy in Frontotemporal Lobar Degeneration
AU - Garibotto, Valentina
AU - Borroni, Barbara
AU - Agosti, Chiara
AU - Premi, Enrico
AU - Alberici, Antonella
AU - Eickhoff, Simon B.
AU - Brambati, Simona M.
AU - Bellelli, Giuseppe
AU - Gasparotti, Roberto
AU - Perani, Daniela
AU - Padovani, Alessandro
PY - 2011/5
Y1 - 2011/5
N2 - Though neuroimaging, pathology and pathophysiology suggest a subcortical and deep cortical involvement in Frontotemporal Lobar Degeneration (FTLD), no studies have comprehensively assessed the associated gray matter (GM) volume changes. We measured caudate, putamen, thalamus, and amygdala GM volume using probabilistic a-priori regions of interest (ROIs) in 53 early FTLD patients (38 behavioral variant FTD [bvFTD], 9 Semantic Dementia [SD], 6 Progressive Non-Fluent Aphasia [PNFA]), and 25 age-matched healthy controls (HC). ANOVA showed significant (P<0.001) main effect of diagnosis, and significant interactions for diagnosis and region, and diagnosis and hemisphere. Post-hoc comparisons with HC showed bilateral GM atrophy in the caudate, putamen and thalamus, in bvFTD; a left-confined GM reduction in the amygdala in SD; and bilateral GM atrophy in the caudate and thalamus, and left-sided GM reduction in the putamen and amygdala in PNFA. Correlation analyses suggested an association between GM volumes and language, psychomotor speed and behavioral disturbances. This study showed a widespread involvement of subcortical and deep cortical GM in early FTLD with patterns specific for clinical entity.
AB - Though neuroimaging, pathology and pathophysiology suggest a subcortical and deep cortical involvement in Frontotemporal Lobar Degeneration (FTLD), no studies have comprehensively assessed the associated gray matter (GM) volume changes. We measured caudate, putamen, thalamus, and amygdala GM volume using probabilistic a-priori regions of interest (ROIs) in 53 early FTLD patients (38 behavioral variant FTD [bvFTD], 9 Semantic Dementia [SD], 6 Progressive Non-Fluent Aphasia [PNFA]), and 25 age-matched healthy controls (HC). ANOVA showed significant (P<0.001) main effect of diagnosis, and significant interactions for diagnosis and region, and diagnosis and hemisphere. Post-hoc comparisons with HC showed bilateral GM atrophy in the caudate, putamen and thalamus, in bvFTD; a left-confined GM reduction in the amygdala in SD; and bilateral GM atrophy in the caudate and thalamus, and left-sided GM reduction in the putamen and amygdala in PNFA. Correlation analyses suggested an association between GM volumes and language, psychomotor speed and behavioral disturbances. This study showed a widespread involvement of subcortical and deep cortical GM in early FTLD with patterns specific for clinical entity.
KW - Basal ganglia
KW - Behavioral variant Frontotemporal Dementia
KW - Frontotemporal Lobar Degeneration
KW - Probabilistic atlases
KW - Progressive Non-Fluent Aphasia
KW - Semantic Dementia
UR - http://www.scopus.com/inward/record.url?scp=79954605057&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79954605057&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2009.05.004
DO - 10.1016/j.neurobiolaging.2009.05.004
M3 - Article
C2 - 19501427
AN - SCOPUS:79954605057
VL - 32
SP - 875
EP - 884
JO - Neurobiology of Aging
JF - Neurobiology of Aging
SN - 0197-4580
IS - 5
ER -