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Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging

BACKGROUND AND AIM: We evaluated whether diffusion kurtosis and tensor imaging (DKI/DTI) could reveal microstructural alterations in the brains of patients with functional gastrointestinal disorders (FGIDs), and whether imaging findings were correlated with health‐related quality of life (HRQOL). ME...

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Autores principales: Chiba, Toshimi, Ito, Kenji, Mori, Futoshi, Sasaki, Makoto, Matsumoto, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578273/
https://www.ncbi.nlm.nih.gov/pubmed/33102770
http://dx.doi.org/10.1002/jgh3.12375
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author Chiba, Toshimi
Ito, Kenji
Mori, Futoshi
Sasaki, Makoto
Matsumoto, Takayuki
author_facet Chiba, Toshimi
Ito, Kenji
Mori, Futoshi
Sasaki, Makoto
Matsumoto, Takayuki
author_sort Chiba, Toshimi
collection PubMed
description BACKGROUND AND AIM: We evaluated whether diffusion kurtosis and tensor imaging (DKI/DTI) could reveal microstructural alterations in the brains of patients with functional gastrointestinal disorders (FGIDs), and whether imaging findings were correlated with health‐related quality of life (HRQOL). METHODS: Twelve patients with FGIDs fulfilling the Rome IV criteria, and seven healthy controls were examined using a 3 T magnetic resonance (MR) scanner. Tract‐based spatial statistics and regions of interest analyses were performed to compare the mean kurtosis (MK), fractional anisotropy (FA), and mean diffusivity (MD) between patients with FGIDs versus controls. HRQOL was assessed in patients with FGIDs using the eight‐item short form of the Medical Outcome Study Questionnaire (SF‐8) and the Gastrointestinal Symptom Rating Scale. RESULTS: Patients with FGIDs had extensive, widespread regions of reduced MD in the white matter in comparison with healthy controls, whereas no significant differences were observed in MK and FA. No significant differences in deep gray matter for the MK, FA, and MD values were observed between patients with FGIDs and controls. In patients with FGIDs, the FA values in the globus pallidus had a significant and negative correlation with SF‐8 (a mental component summary) (r = −0.797, P = 0.01 uncorrected for multiple comparisons). CONCLUSIONS: DKI/DTI can help identify microstructural white matter alterations in patients with FGIDs. The FA values in the globus pallidus may be useful for a severity assessment of FGIDs.
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spelling pubmed-75782732020-10-23 Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging Chiba, Toshimi Ito, Kenji Mori, Futoshi Sasaki, Makoto Matsumoto, Takayuki JGH Open Original Articles BACKGROUND AND AIM: We evaluated whether diffusion kurtosis and tensor imaging (DKI/DTI) could reveal microstructural alterations in the brains of patients with functional gastrointestinal disorders (FGIDs), and whether imaging findings were correlated with health‐related quality of life (HRQOL). METHODS: Twelve patients with FGIDs fulfilling the Rome IV criteria, and seven healthy controls were examined using a 3 T magnetic resonance (MR) scanner. Tract‐based spatial statistics and regions of interest analyses were performed to compare the mean kurtosis (MK), fractional anisotropy (FA), and mean diffusivity (MD) between patients with FGIDs versus controls. HRQOL was assessed in patients with FGIDs using the eight‐item short form of the Medical Outcome Study Questionnaire (SF‐8) and the Gastrointestinal Symptom Rating Scale. RESULTS: Patients with FGIDs had extensive, widespread regions of reduced MD in the white matter in comparison with healthy controls, whereas no significant differences were observed in MK and FA. No significant differences in deep gray matter for the MK, FA, and MD values were observed between patients with FGIDs and controls. In patients with FGIDs, the FA values in the globus pallidus had a significant and negative correlation with SF‐8 (a mental component summary) (r = −0.797, P = 0.01 uncorrected for multiple comparisons). CONCLUSIONS: DKI/DTI can help identify microstructural white matter alterations in patients with FGIDs. The FA values in the globus pallidus may be useful for a severity assessment of FGIDs. Wiley Publishing Asia Pty Ltd 2020-06-12 /pmc/articles/PMC7578273/ /pubmed/33102770 http://dx.doi.org/10.1002/jgh3.12375 Text en © 2020 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Chiba, Toshimi
Ito, Kenji
Mori, Futoshi
Sasaki, Makoto
Matsumoto, Takayuki
Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
title Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
title_full Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
title_fullStr Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
title_full_unstemmed Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
title_short Detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
title_sort detection of microstructural white matter alterations in functional gastrointestinal disorders assessed by diffusion kurtosis imaging
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578273/
https://www.ncbi.nlm.nih.gov/pubmed/33102770
http://dx.doi.org/10.1002/jgh3.12375
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