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Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease

BACKGROUND: Corrupted gradient directions (GD) in diffusion weighted images may seriously affect reliability of diffusion tensor imaging (DTI)-based comparisons at the group level. In the present study we employed a quality control (QC) algorithm to eliminate corrupted gradient directions from DTI d...

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Autores principales: Müller, Hans-Peter, Kassubek, Jan, Grön, Georg, Sprengelmeyer, Reiner, Ludolph, Albert C, Klöppel, Stefan, Hobbs, Nicola Z, Roos, Raymund AC, Duerr, Alexandra, Tabrizi, Sarah J, Orth, Michael, Süssmuth, Sigurd D, Landwehrmeyer, G Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162922/
https://www.ncbi.nlm.nih.gov/pubmed/25178314
http://dx.doi.org/10.1186/1475-925X-13-128
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author Müller, Hans-Peter
Kassubek, Jan
Grön, Georg
Sprengelmeyer, Reiner
Ludolph, Albert C
Klöppel, Stefan
Hobbs, Nicola Z
Roos, Raymund AC
Duerr, Alexandra
Tabrizi, Sarah J
Orth, Michael
Süssmuth, Sigurd D
Landwehrmeyer, G Bernhard
author_facet Müller, Hans-Peter
Kassubek, Jan
Grön, Georg
Sprengelmeyer, Reiner
Ludolph, Albert C
Klöppel, Stefan
Hobbs, Nicola Z
Roos, Raymund AC
Duerr, Alexandra
Tabrizi, Sarah J
Orth, Michael
Süssmuth, Sigurd D
Landwehrmeyer, G Bernhard
author_sort Müller, Hans-Peter
collection PubMed
description BACKGROUND: Corrupted gradient directions (GD) in diffusion weighted images may seriously affect reliability of diffusion tensor imaging (DTI)-based comparisons at the group level. In the present study we employed a quality control (QC) algorithm to eliminate corrupted gradient directions from DTI data. We then assessed effects of this procedure on comparisons between Huntington disease (HD) subjects and controls at the group level. METHODS: Sixty-one HD patients in early stages and forty matched healthy controls were studied in a longitudinal design (baseline and two follow-ups at three time points over 15 months), in a multicenter setting with similar acquisition protocols on four different MR scanners at four European study sites. A QC algorithm was used to identify corrupted GD in DTI data sets. Differences in fractional anisotropy (FA) maps at the group level with and without elimination of corrupted GD were analyzed. RESULTS: The elimination of corrupted GD had an impact on individual FA maps as well as on cross-sectional group comparisons between HD subjects and controls. Following application of the QC algorithm, less small clusters of FA changes were observed, compared to the analysis without QC. However, the main pattern of regional reductions and increases in FA values with and without QC-based elimination of corrupted GD was unchanged. CONCLUSION: An impact on the result patterns of the comparison of FA maps between HD subjects and controls was observed depending on whether QC-based elimination of corrupted GD was performed. QC-based elimination of corrupted GD in DTI scans reduces the risk of type I and type II errors in cross-sectional group comparison of FA maps contributing to an increase in reliability and stability of group comparisons.
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spelling pubmed-41629222014-09-14 Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease Müller, Hans-Peter Kassubek, Jan Grön, Georg Sprengelmeyer, Reiner Ludolph, Albert C Klöppel, Stefan Hobbs, Nicola Z Roos, Raymund AC Duerr, Alexandra Tabrizi, Sarah J Orth, Michael Süssmuth, Sigurd D Landwehrmeyer, G Bernhard Biomed Eng Online Research BACKGROUND: Corrupted gradient directions (GD) in diffusion weighted images may seriously affect reliability of diffusion tensor imaging (DTI)-based comparisons at the group level. In the present study we employed a quality control (QC) algorithm to eliminate corrupted gradient directions from DTI data. We then assessed effects of this procedure on comparisons between Huntington disease (HD) subjects and controls at the group level. METHODS: Sixty-one HD patients in early stages and forty matched healthy controls were studied in a longitudinal design (baseline and two follow-ups at three time points over 15 months), in a multicenter setting with similar acquisition protocols on four different MR scanners at four European study sites. A QC algorithm was used to identify corrupted GD in DTI data sets. Differences in fractional anisotropy (FA) maps at the group level with and without elimination of corrupted GD were analyzed. RESULTS: The elimination of corrupted GD had an impact on individual FA maps as well as on cross-sectional group comparisons between HD subjects and controls. Following application of the QC algorithm, less small clusters of FA changes were observed, compared to the analysis without QC. However, the main pattern of regional reductions and increases in FA values with and without QC-based elimination of corrupted GD was unchanged. CONCLUSION: An impact on the result patterns of the comparison of FA maps between HD subjects and controls was observed depending on whether QC-based elimination of corrupted GD was performed. QC-based elimination of corrupted GD in DTI scans reduces the risk of type I and type II errors in cross-sectional group comparison of FA maps contributing to an increase in reliability and stability of group comparisons. BioMed Central 2014-09-01 /pmc/articles/PMC4162922/ /pubmed/25178314 http://dx.doi.org/10.1186/1475-925X-13-128 Text en © Müller et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Müller, Hans-Peter
Kassubek, Jan
Grön, Georg
Sprengelmeyer, Reiner
Ludolph, Albert C
Klöppel, Stefan
Hobbs, Nicola Z
Roos, Raymund AC
Duerr, Alexandra
Tabrizi, Sarah J
Orth, Michael
Süssmuth, Sigurd D
Landwehrmeyer, G Bernhard
Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
title Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
title_full Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
title_fullStr Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
title_full_unstemmed Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
title_short Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease
title_sort impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in huntington disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162922/
https://www.ncbi.nlm.nih.gov/pubmed/25178314
http://dx.doi.org/10.1186/1475-925X-13-128
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