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The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis
Volumetric magnetic resonance imaging (MRI) atrophy is a hallmark of Rasmussen’s encephalitis (RE). Here, we aim to investigate voxel-wise gray matter (GM) atrophy in RE, and its associations with glucose hypometabolism and neurotransmitter distribution utilizing MRI and PET data. In this study, fif...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713113/ https://www.ncbi.nlm.nih.gov/pubmed/34952352 http://dx.doi.org/10.1016/j.nicl.2021.102918 |
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author | Tang, Chongyang Ren, Peng Ma, Kaiqiang Li, Siyang Wang, Xiongfei Guan, Yuguang Zhou, Jian Li, Tianfu Liang, Xia Luan, Guoming |
author_facet | Tang, Chongyang Ren, Peng Ma, Kaiqiang Li, Siyang Wang, Xiongfei Guan, Yuguang Zhou, Jian Li, Tianfu Liang, Xia Luan, Guoming |
author_sort | Tang, Chongyang |
collection | PubMed |
description | Volumetric magnetic resonance imaging (MRI) atrophy is a hallmark of Rasmussen’s encephalitis (RE). Here, we aim to investigate voxel-wise gray matter (GM) atrophy in RE, and its associations with glucose hypometabolism and neurotransmitter distribution utilizing MRI and PET data. In this study, fifteen RE patients and fourteen MRI normal subjects were included in this study. Voxel-wise GM volume and glucose metabolic uptake were evaluated using structural MRI and FDG-PET images, respectively. Spatial Spearman’s correlation was performed between GM atrophy of RE with FDG uptake alterations, and neurotransmitter distributions provided in the JuSpace toolbox. Compared with the control group, RE patients displayed extensive GM volume loss not only in the ipsilateral hemisphere, but also in the frontal lobe, basal ganglia, and cerebellum in the contralateral hemisphere. Within the RE group, the insular and temporal cortices exhibited significantly more GM atrophy on the ipsilesional than the contralesional side. FDG-PET data revealed significant hypometabolism in areas surrounding the insular cortices in the ipsilesional hemisphere. RE-related GM volumetric atrophy was spatially correlated with hypomebolism in FDG uptake, and with spatial distribution of the dopaminergic and serotonergic neurotransmitter systems. The spatial concordance of morphological changes with metabolic abnormalities suggest FDG-PET offers potential value for RE diagnosis. The GM alterations associated with neurotransmitter distribution map could provide novel insight in understanding the neuropathological mechanisms and clinical feature of RE. |
format | Online Article Text |
id | pubmed-8713113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87131132022-01-05 The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis Tang, Chongyang Ren, Peng Ma, Kaiqiang Li, Siyang Wang, Xiongfei Guan, Yuguang Zhou, Jian Li, Tianfu Liang, Xia Luan, Guoming Neuroimage Clin Regular Article Volumetric magnetic resonance imaging (MRI) atrophy is a hallmark of Rasmussen’s encephalitis (RE). Here, we aim to investigate voxel-wise gray matter (GM) atrophy in RE, and its associations with glucose hypometabolism and neurotransmitter distribution utilizing MRI and PET data. In this study, fifteen RE patients and fourteen MRI normal subjects were included in this study. Voxel-wise GM volume and glucose metabolic uptake were evaluated using structural MRI and FDG-PET images, respectively. Spatial Spearman’s correlation was performed between GM atrophy of RE with FDG uptake alterations, and neurotransmitter distributions provided in the JuSpace toolbox. Compared with the control group, RE patients displayed extensive GM volume loss not only in the ipsilateral hemisphere, but also in the frontal lobe, basal ganglia, and cerebellum in the contralateral hemisphere. Within the RE group, the insular and temporal cortices exhibited significantly more GM atrophy on the ipsilesional than the contralesional side. FDG-PET data revealed significant hypometabolism in areas surrounding the insular cortices in the ipsilesional hemisphere. RE-related GM volumetric atrophy was spatially correlated with hypomebolism in FDG uptake, and with spatial distribution of the dopaminergic and serotonergic neurotransmitter systems. The spatial concordance of morphological changes with metabolic abnormalities suggest FDG-PET offers potential value for RE diagnosis. The GM alterations associated with neurotransmitter distribution map could provide novel insight in understanding the neuropathological mechanisms and clinical feature of RE. Elsevier 2021-12-20 /pmc/articles/PMC8713113/ /pubmed/34952352 http://dx.doi.org/10.1016/j.nicl.2021.102918 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Tang, Chongyang Ren, Peng Ma, Kaiqiang Li, Siyang Wang, Xiongfei Guan, Yuguang Zhou, Jian Li, Tianfu Liang, Xia Luan, Guoming The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis |
title | The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis |
title_full | The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis |
title_fullStr | The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis |
title_full_unstemmed | The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis |
title_short | The correspondence between morphometric MRI and metabolic profile in Rasmussen’s encephalitis |
title_sort | correspondence between morphometric mri and metabolic profile in rasmussen’s encephalitis |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713113/ https://www.ncbi.nlm.nih.gov/pubmed/34952352 http://dx.doi.org/10.1016/j.nicl.2021.102918 |
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