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Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study

OBJECTIVE: Friedreich's ataxia (FRDA) is a spinocerebellar degenerative disorder, in which cognitive deficits are sparsely explored. In this behavioral and multimodal magnetic resonance imaging (MRI) study, we investigated the neurocognitive profile and cortico‐cerebellar dysfunctions underlyin...

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Autores principales: Dogan, Imis, Tinnemann, Eugenie, Romanzetti, Sandro, Mirzazade, Shahram, Costa, Ana S., Werner, Cornelius J., Heim, Stefan, Fedosov, Kathrin, Schulz, Stefanie, Timmann, Dagmar, Giordano, Ilaria A., Klockgether, Thomas, Schulz, Jörg B., Reetz, Kathrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999591/
https://www.ncbi.nlm.nih.gov/pubmed/27606341
http://dx.doi.org/10.1002/acn3.315
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author Dogan, Imis
Tinnemann, Eugenie
Romanzetti, Sandro
Mirzazade, Shahram
Costa, Ana S.
Werner, Cornelius J.
Heim, Stefan
Fedosov, Kathrin
Schulz, Stefanie
Timmann, Dagmar
Giordano, Ilaria A.
Klockgether, Thomas
Schulz, Jörg B.
Reetz, Kathrin
author_facet Dogan, Imis
Tinnemann, Eugenie
Romanzetti, Sandro
Mirzazade, Shahram
Costa, Ana S.
Werner, Cornelius J.
Heim, Stefan
Fedosov, Kathrin
Schulz, Stefanie
Timmann, Dagmar
Giordano, Ilaria A.
Klockgether, Thomas
Schulz, Jörg B.
Reetz, Kathrin
author_sort Dogan, Imis
collection PubMed
description OBJECTIVE: Friedreich's ataxia (FRDA) is a spinocerebellar degenerative disorder, in which cognitive deficits are sparsely explored. In this behavioral and multimodal magnetic resonance imaging (MRI) study, we investigated the neurocognitive profile and cortico‐cerebellar dysfunctions underlying executive functioning in individuals with FRDA. METHODS: 22 FRDA patients and 22 controls were clinically and neuropsychologically examined. Fifteen of each underwent structural and functional MRI using a verbal‐fluency task with phonemic and semantic conditions. Gray (GM) and white matter (WM) alterations were assessed by means of voxel‐based morphometry and diffusion‐tensor imaging. RESULTS: The neuropsychological profile demonstrated deficits in verbal fluency, working memory and social cognition. Functional MRI data showed most pronounced group‐differences in phonemic fluency with patients exhibiting enhanced activity in the cerebellum (VI, Crus I), fronto‐insular, premotor and temporo‐occipital regions. The semantic condition only revealed reduced activity in the anterior cerebellum; for overt speech, we found increased activity in the motor cortex. Functional connectivity‐analysis showed higher co‐activation within cerebellar and cortical regions, respectively, and impaired interregional coupling between the cerebellum and fronto‐insular cortex for phonemic processing, which was also related to poorer task performance. GM reduction in FRDA was mainly found in lobule VI, whereas WM degeneration was more pronounced including brainstem, cerebellum, and cortex. Decreased cerebellar GM was associated with enhanced activity in the fronto‐insular cortex, while loss of WM integrity may translate cortico‐cerebellar pathway disruptions. INTERPRETATION: The pattern of increased neural response with both cerebellar and cortical involvement underlying executive functioning indicates functional reorganization driven by disease‐related structural damage in FRDA.
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spelling pubmed-49995912016-09-07 Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study Dogan, Imis Tinnemann, Eugenie Romanzetti, Sandro Mirzazade, Shahram Costa, Ana S. Werner, Cornelius J. Heim, Stefan Fedosov, Kathrin Schulz, Stefanie Timmann, Dagmar Giordano, Ilaria A. Klockgether, Thomas Schulz, Jörg B. Reetz, Kathrin Ann Clin Transl Neurol Research Paper OBJECTIVE: Friedreich's ataxia (FRDA) is a spinocerebellar degenerative disorder, in which cognitive deficits are sparsely explored. In this behavioral and multimodal magnetic resonance imaging (MRI) study, we investigated the neurocognitive profile and cortico‐cerebellar dysfunctions underlying executive functioning in individuals with FRDA. METHODS: 22 FRDA patients and 22 controls were clinically and neuropsychologically examined. Fifteen of each underwent structural and functional MRI using a verbal‐fluency task with phonemic and semantic conditions. Gray (GM) and white matter (WM) alterations were assessed by means of voxel‐based morphometry and diffusion‐tensor imaging. RESULTS: The neuropsychological profile demonstrated deficits in verbal fluency, working memory and social cognition. Functional MRI data showed most pronounced group‐differences in phonemic fluency with patients exhibiting enhanced activity in the cerebellum (VI, Crus I), fronto‐insular, premotor and temporo‐occipital regions. The semantic condition only revealed reduced activity in the anterior cerebellum; for overt speech, we found increased activity in the motor cortex. Functional connectivity‐analysis showed higher co‐activation within cerebellar and cortical regions, respectively, and impaired interregional coupling between the cerebellum and fronto‐insular cortex for phonemic processing, which was also related to poorer task performance. GM reduction in FRDA was mainly found in lobule VI, whereas WM degeneration was more pronounced including brainstem, cerebellum, and cortex. Decreased cerebellar GM was associated with enhanced activity in the fronto‐insular cortex, while loss of WM integrity may translate cortico‐cerebellar pathway disruptions. INTERPRETATION: The pattern of increased neural response with both cerebellar and cortical involvement underlying executive functioning indicates functional reorganization driven by disease‐related structural damage in FRDA. John Wiley and Sons Inc. 2016-06-21 /pmc/articles/PMC4999591/ /pubmed/27606341 http://dx.doi.org/10.1002/acn3.315 Text en © 2016 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Paper
Dogan, Imis
Tinnemann, Eugenie
Romanzetti, Sandro
Mirzazade, Shahram
Costa, Ana S.
Werner, Cornelius J.
Heim, Stefan
Fedosov, Kathrin
Schulz, Stefanie
Timmann, Dagmar
Giordano, Ilaria A.
Klockgether, Thomas
Schulz, Jörg B.
Reetz, Kathrin
Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study
title Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study
title_full Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study
title_fullStr Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study
title_full_unstemmed Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study
title_short Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study
title_sort cognition in friedreich's ataxia: a behavioral and multimodal imaging study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4999591/
https://www.ncbi.nlm.nih.gov/pubmed/27606341
http://dx.doi.org/10.1002/acn3.315
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