Crossed aphasia confirmed by fMRI in a case with nonfluent variant of primary progressive aphasia carrying a GRN mutation.
Crossed aphasia
Functional MRI (fMRI)
Nonfluent/agrammatic primary progressive aphasia
Progranulin (GRN) mutation
Journal
Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
13
03
2019
accepted:
23
03
2019
revised:
22
03
2019
pubmed:
30
3
2019
medline:
14
8
2019
entrez:
30
3
2019
Statut:
ppublish
Résumé
To characterize patterns of language lateralization in a right-handed woman with nonfluent/agrammatic primary progressive aphasia (nfvPPA) clinical picture despite showing a prevalent right-sided brain damage. We report a case of a 58-year-old woman with nfvPPA diagnosis (age at onset = 55) previously described as a crossed aphasia case with progranulin mutation. At 2 years from the first visit, patient underwent 3DT1-weighted and a task-based functional MRI (fMRI). During the fMRI task, she was asked to perform a letter fluency test as the task of interest and to count forward as the control condition. Image processing and data analysis were performed using SPM12 and the effect of each task was tested at p < 0.05 FWE corrected. The structural MRI confirmed a widespread right fronto-temporal atrophy mainly involving the right inferior frontal gyrus. During the letter fluency task, we observed an increased activation centered at the right inferior orbitofrontal gyrus and right middle frontal gyrus. By reducing the threshold, the pattern of functional activation was still dramatically prevalent at the right side. We provided evidence of the right language lateralization in a previously suspected crossed nfvPPA. Despite the long disease duration and the large amount of atrophy at the right side, there was no fMRI evidence of a left-hemisphere contribution to language function. We might speculate that compensatory effects do not appear when the premorbid language lateralization is purely right. The investigation of the underlying functional brain substrates in crossed nfvPPA cases may help understanding disease vulnerability in these neurodegenerative conditions.
Identifiants
pubmed: 30923936
doi: 10.1007/s00415-019-09298-w
pii: 10.1007/s00415-019-09298-w
doi:
Substances chimiques
GRN protein, human
0
Progranulins
0
Oxygen
S88TT14065
Types de publication
Case Reports
Journal Article
Langues
eng
Pagination
1274-1279Subventions
Organisme : Ministero della Salute
ID : GR-2011-02351217
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