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Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis

OBJECTIVE: Psychosis is an important comorbidity in epilepsy, but its pathophysiology is still unknown. The imaging modality (18)F‐fluorodeoxyglucose‐positron emission tomography ((18)F‐FDG PET) is widely used to measure brain glucose metabolism, and we speculated that (18)F‐FDG PET may detect chara...

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Autores principales: Sone, Daichi, Sato, Noriko, Shigemoto, Yoko, Kimura, Yukio, Matsuda, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712471/
https://www.ncbi.nlm.nih.gov/pubmed/35977826
http://dx.doi.org/10.1002/epi4.12645
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author Sone, Daichi
Sato, Noriko
Shigemoto, Yoko
Kimura, Yukio
Matsuda, Hiroshi
author_facet Sone, Daichi
Sato, Noriko
Shigemoto, Yoko
Kimura, Yukio
Matsuda, Hiroshi
author_sort Sone, Daichi
collection PubMed
description OBJECTIVE: Psychosis is an important comorbidity in epilepsy, but its pathophysiology is still unknown. The imaging modality (18)F‐fluorodeoxyglucose‐positron emission tomography ((18)F‐FDG PET) is widely used to measure brain glucose metabolism, and we speculated that (18)F‐FDG PET may detect characteristic alteration patterns in individuals with temporal lobe epilepsy (TLE) and psychosis. METHODS: We enrolled 13 patients with TLE and interictal psychosis (TLE‐P) and 21 patients with TLE without psychosis (TLE‐N). All underwent interictal (18)F‐FDG‐PET scanning. Statistical Parametric Mapping (SPM)12 software was used for the normalization process, and we performed a voxel‐wise comparison of the TLE‐P and TLE‐N groups. RESULTS: Cerebral hypometabolic areas were observed in the ipsilateral temporal pole to hippocampus in both patient groups. In the TLE‐P group, the voxel‐wise comparison revealed significantly increased (18)F‐FDG signals in the upper cerebellum, superior cerebellar peduncle, and midbrain. There were no significant between‐group metabolic differences around the focus or other cerebral areas. SIGNIFICANCE: Our results demonstrated significant hypermetabolism around the upper cerebellum in patients with TLE and interictal psychosis compared to patients with TLE without psychosis. These findings may reflect the involvement of the cerebellum in the underlying neurobiology of interictal psychosis and could contribute to a better understanding of this disorder.
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spelling pubmed-97124712022-12-02 Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis Sone, Daichi Sato, Noriko Shigemoto, Yoko Kimura, Yukio Matsuda, Hiroshi Epilepsia Open Original Articles OBJECTIVE: Psychosis is an important comorbidity in epilepsy, but its pathophysiology is still unknown. The imaging modality (18)F‐fluorodeoxyglucose‐positron emission tomography ((18)F‐FDG PET) is widely used to measure brain glucose metabolism, and we speculated that (18)F‐FDG PET may detect characteristic alteration patterns in individuals with temporal lobe epilepsy (TLE) and psychosis. METHODS: We enrolled 13 patients with TLE and interictal psychosis (TLE‐P) and 21 patients with TLE without psychosis (TLE‐N). All underwent interictal (18)F‐FDG‐PET scanning. Statistical Parametric Mapping (SPM)12 software was used for the normalization process, and we performed a voxel‐wise comparison of the TLE‐P and TLE‐N groups. RESULTS: Cerebral hypometabolic areas were observed in the ipsilateral temporal pole to hippocampus in both patient groups. In the TLE‐P group, the voxel‐wise comparison revealed significantly increased (18)F‐FDG signals in the upper cerebellum, superior cerebellar peduncle, and midbrain. There were no significant between‐group metabolic differences around the focus or other cerebral areas. SIGNIFICANCE: Our results demonstrated significant hypermetabolism around the upper cerebellum in patients with TLE and interictal psychosis compared to patients with TLE without psychosis. These findings may reflect the involvement of the cerebellum in the underlying neurobiology of interictal psychosis and could contribute to a better understanding of this disorder. John Wiley and Sons Inc. 2022-08-30 /pmc/articles/PMC9712471/ /pubmed/35977826 http://dx.doi.org/10.1002/epi4.12645 Text en © 2022 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 Original Articles
Sone, Daichi
Sato, Noriko
Shigemoto, Yoko
Kimura, Yukio
Matsuda, Hiroshi
Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
title Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
title_full Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
title_fullStr Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
title_full_unstemmed Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
title_short Upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
title_sort upper cerebellar glucose hypermetabolism in patients with temporal lobe epilepsy and interictal psychosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9712471/
https://www.ncbi.nlm.nih.gov/pubmed/35977826
http://dx.doi.org/10.1002/epi4.12645
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