TY - JOUR
T1 - Degenerative and Vascular Fluent Aphasia: Looking for Differences
AU - Silveri, Maria Caterina
AU - Di Tella, Sonia
AU - Magni, Eugenio
AU - Pepe, Fulvio
AU - Lassandro Pepe, Francesca
AU - Leone, Edoardo
AU - Piludu, Francesca
AU - Colosimo, Cesare
AU - Ciccarelli, Nicoletta
PY - 2019
Y1 - 2019
N2 - Objective:To investigate whether the characteristics of language disorders of degenerative and vascular aphasias depend on the underlying neuropathology.Methods:Logopenic variant/mixed primary progressive aphasics (lvmPPA; n=18) and poststroke fluent aphasics (PSA; n=11) underwent a neuropsychological examination and an assessment of the macro-and microlinguistic aspects of language. A principal component analysis and a cluster analysis applying a two-group solution were performed on the scores obtained from the neuropsychological and language examination.Results:Global cognition, lexical-semantic, and morphosyntactic components, and two components loading macrolinguistic variables, were extracted by the principal component analysis. A first cluster of 18 participants (14 lvmPPA and 4 PSA) and a second cluster of 11 participants (4 lvmPPA and 7 PSA) were identified. Participants in the first cluster were significantly more impaired than those in the second cluster in global cognition, lexical-semantic, and morphosyntactic components. Macrolinguistic components did not differentiate the two clusters. lvmPPA in the first cluster showed bilateral cortical thinning (greater on the left), whereas lvmPPA in the second cluster showed atrophy only in the left. Participants with PSA in both clusters showed vascular lesions encompassing the posterior left perisylvian regions. Underestimation of the severity of the leukoencephalopathy and damage of the interhemispheric connectivity might be responsible for the inclusion of PSA individuals in the first cluster, despite a unilateral lesion.Conclusions:Lesion localization is the main factor that determines the characteristics of aphasic deficits. Etiology indirectly acts through a different sensitivity of the brain regions to various pathologies.
AB - Objective:To investigate whether the characteristics of language disorders of degenerative and vascular aphasias depend on the underlying neuropathology.Methods:Logopenic variant/mixed primary progressive aphasics (lvmPPA; n=18) and poststroke fluent aphasics (PSA; n=11) underwent a neuropsychological examination and an assessment of the macro-and microlinguistic aspects of language. A principal component analysis and a cluster analysis applying a two-group solution were performed on the scores obtained from the neuropsychological and language examination.Results:Global cognition, lexical-semantic, and morphosyntactic components, and two components loading macrolinguistic variables, were extracted by the principal component analysis. A first cluster of 18 participants (14 lvmPPA and 4 PSA) and a second cluster of 11 participants (4 lvmPPA and 7 PSA) were identified. Participants in the first cluster were significantly more impaired than those in the second cluster in global cognition, lexical-semantic, and morphosyntactic components. Macrolinguistic components did not differentiate the two clusters. lvmPPA in the first cluster showed bilateral cortical thinning (greater on the left), whereas lvmPPA in the second cluster showed atrophy only in the left. Participants with PSA in both clusters showed vascular lesions encompassing the posterior left perisylvian regions. Underestimation of the severity of the leukoencephalopathy and damage of the interhemispheric connectivity might be responsible for the inclusion of PSA individuals in the first cluster, despite a unilateral lesion.Conclusions:Lesion localization is the main factor that determines the characteristics of aphasic deficits. Etiology indirectly acts through a different sensitivity of the brain regions to various pathologies.
KW - morphosyntactic disorder
KW - poststroke fluent aphasia
KW - primary progressive aphasia
KW - semantic deficit
KW - morphosyntactic disorder
KW - poststroke fluent aphasia
KW - primary progressive aphasia
KW - semantic deficit
UR - http://hdl.handle.net/10807/147745
UR - http://www.cogbehavneurol.com
U2 - 10.1097/WNN.0000000000000207
DO - 10.1097/WNN.0000000000000207
M3 - Article
SN - 1543-3633
VL - 32
SP - 225
EP - 235
JO - Cognitive and Behavioral Neurology
JF - Cognitive and Behavioral Neurology
ER -