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Diffusion tensor imaging in the characterization of multiple system atrophy

PURPOSE: Multiple system atrophy (MSA) is a rare neurodegenerative disease that remains poorly understood, and the diagnosis of MSA continues to be challenging. We endeavored to improve the diagnostic process and understanding of in vivo characteristics of MSA by diffusion tensor imaging (DTI). MATE...

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Autores principales: Rulseh, Aaron Michael, Keller, Jiri, Rusz, Jan, Syka, Michael, Brozova, Hana, Rusina, Robert, Havrankova, Petra, Zarubova, Katerina, Malikova, Hana, Jech, Robert, Vymazal, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008640/
https://www.ncbi.nlm.nih.gov/pubmed/27616888
http://dx.doi.org/10.2147/NDT.S109094
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author Rulseh, Aaron Michael
Keller, Jiri
Rusz, Jan
Syka, Michael
Brozova, Hana
Rusina, Robert
Havrankova, Petra
Zarubova, Katerina
Malikova, Hana
Jech, Robert
Vymazal, Josef
author_facet Rulseh, Aaron Michael
Keller, Jiri
Rusz, Jan
Syka, Michael
Brozova, Hana
Rusina, Robert
Havrankova, Petra
Zarubova, Katerina
Malikova, Hana
Jech, Robert
Vymazal, Josef
author_sort Rulseh, Aaron Michael
collection PubMed
description PURPOSE: Multiple system atrophy (MSA) is a rare neurodegenerative disease that remains poorly understood, and the diagnosis of MSA continues to be challenging. We endeavored to improve the diagnostic process and understanding of in vivo characteristics of MSA by diffusion tensor imaging (DTI). MATERIALS AND METHODS: Twenty MSA subjects, ten parkinsonian dominant (MSA-P), ten cerebellar dominant (MSA-C), and 20 healthy volunteer subjects were recruited. Fractional anisotropy, mean diffusivity, radial diffusivity, and axial diffusivity maps were processed using tract-based spatial statistics. Diffusion data were additionally evaluated in the basal ganglia. A support vector machine was used to assess diagnostic utility, leave-one-out cross-validation in the evaluation of classification schemes, and receiver operating characteristic analyses to determine cutoff values. RESULTS: We detected widespread changes in the brain white matter of MSA subjects; however, no group-wise differences were found between MSA-C and MSA-P subgroups. Altered DTI metrics in the putamen and middle cerebellar peduncles were associated with a positive parkinsonian and cerebellar phenotype, respectively. Concerning clinical applicability, we achieved high classification performance on mean diffusivity data in the combined bilateral putamen and middle cerebellar peduncle (accuracy 90.3%±9%, sensitivity 86.5%±11%, and specificity 99.3%±4%). CONCLUSION: DTI in the middle cerebellar peduncle and putamen may be used in the diagnosis of MSA with a high degree of accuracy.
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spelling pubmed-50086402016-09-09 Diffusion tensor imaging in the characterization of multiple system atrophy Rulseh, Aaron Michael Keller, Jiri Rusz, Jan Syka, Michael Brozova, Hana Rusina, Robert Havrankova, Petra Zarubova, Katerina Malikova, Hana Jech, Robert Vymazal, Josef Neuropsychiatr Dis Treat Original Research PURPOSE: Multiple system atrophy (MSA) is a rare neurodegenerative disease that remains poorly understood, and the diagnosis of MSA continues to be challenging. We endeavored to improve the diagnostic process and understanding of in vivo characteristics of MSA by diffusion tensor imaging (DTI). MATERIALS AND METHODS: Twenty MSA subjects, ten parkinsonian dominant (MSA-P), ten cerebellar dominant (MSA-C), and 20 healthy volunteer subjects were recruited. Fractional anisotropy, mean diffusivity, radial diffusivity, and axial diffusivity maps were processed using tract-based spatial statistics. Diffusion data were additionally evaluated in the basal ganglia. A support vector machine was used to assess diagnostic utility, leave-one-out cross-validation in the evaluation of classification schemes, and receiver operating characteristic analyses to determine cutoff values. RESULTS: We detected widespread changes in the brain white matter of MSA subjects; however, no group-wise differences were found between MSA-C and MSA-P subgroups. Altered DTI metrics in the putamen and middle cerebellar peduncles were associated with a positive parkinsonian and cerebellar phenotype, respectively. Concerning clinical applicability, we achieved high classification performance on mean diffusivity data in the combined bilateral putamen and middle cerebellar peduncle (accuracy 90.3%±9%, sensitivity 86.5%±11%, and specificity 99.3%±4%). CONCLUSION: DTI in the middle cerebellar peduncle and putamen may be used in the diagnosis of MSA with a high degree of accuracy. Dove Medical Press 2016-08-26 /pmc/articles/PMC5008640/ /pubmed/27616888 http://dx.doi.org/10.2147/NDT.S109094 Text en © 2016 Rulseh et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Rulseh, Aaron Michael
Keller, Jiri
Rusz, Jan
Syka, Michael
Brozova, Hana
Rusina, Robert
Havrankova, Petra
Zarubova, Katerina
Malikova, Hana
Jech, Robert
Vymazal, Josef
Diffusion tensor imaging in the characterization of multiple system atrophy
title Diffusion tensor imaging in the characterization of multiple system atrophy
title_full Diffusion tensor imaging in the characterization of multiple system atrophy
title_fullStr Diffusion tensor imaging in the characterization of multiple system atrophy
title_full_unstemmed Diffusion tensor imaging in the characterization of multiple system atrophy
title_short Diffusion tensor imaging in the characterization of multiple system atrophy
title_sort diffusion tensor imaging in the characterization of multiple system atrophy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008640/
https://www.ncbi.nlm.nih.gov/pubmed/27616888
http://dx.doi.org/10.2147/NDT.S109094
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