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Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies

BACKGROUND: Previous positron emission tomography studies have reported the changes of cerebral glucose metabolism in bipolar disorder. However, the findings across studies remain controversial, containing differing results. METHODS: A systematic literature search of the PubMed, Embase, Cochrane Lib...

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Autores principales: Wu, Chujun, Ren, Chutong, Teng, Ziwei, Li, Sujuan, Silva, Floyd, Wu, Haishan, Chen, Jindong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119802/
https://www.ncbi.nlm.nih.gov/pubmed/33769704
http://dx.doi.org/10.1002/brb3.2117
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author Wu, Chujun
Ren, Chutong
Teng, Ziwei
Li, Sujuan
Silva, Floyd
Wu, Haishan
Chen, Jindong
author_facet Wu, Chujun
Ren, Chutong
Teng, Ziwei
Li, Sujuan
Silva, Floyd
Wu, Haishan
Chen, Jindong
author_sort Wu, Chujun
collection PubMed
description BACKGROUND: Previous positron emission tomography studies have reported the changes of cerebral glucose metabolism in bipolar disorder. However, the findings across studies remain controversial, containing differing results. METHODS: A systematic literature search of the PubMed, Embase, Cochrane Library, and Web of Science databases was conducted. We conducted a voxel‐wide meta‐analysis of cerebral glucose metabolism studies, using the seed‐based mapping approach, in patients with bipolar disorder (BD). RESULTS: We identified 7 studies suitable for inclusion, which included a total of 126 individuals with BD and 160 healthy controls. The most consistent and robust findings were an increase in cerebral glucose metabolism in the right precentral gyrus and a decrease in the left superior temporal gyrus, left middle temporal gyrus, and cerebellum. Additionally, the sex distribution and illness duration had significant moderating effects on cerebral glucose metabolism alterations. CONCLUSIONS: Cerebral glucose metabolism alterations in these brain regions are likely to reflect the disease‐related functional abnormalities such as emotion and cognition. These findings contribute to a better understanding of the neurobiological underpinnings of bipolar disorder. Limitations. This study was done at a study level and cannot be addressed at the patient level. Subgroup analysis of BD I and BD II is not possible due to limited literature data.
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spelling pubmed-81198022021-05-20 Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies Wu, Chujun Ren, Chutong Teng, Ziwei Li, Sujuan Silva, Floyd Wu, Haishan Chen, Jindong Brain Behav Original Research BACKGROUND: Previous positron emission tomography studies have reported the changes of cerebral glucose metabolism in bipolar disorder. However, the findings across studies remain controversial, containing differing results. METHODS: A systematic literature search of the PubMed, Embase, Cochrane Library, and Web of Science databases was conducted. We conducted a voxel‐wide meta‐analysis of cerebral glucose metabolism studies, using the seed‐based mapping approach, in patients with bipolar disorder (BD). RESULTS: We identified 7 studies suitable for inclusion, which included a total of 126 individuals with BD and 160 healthy controls. The most consistent and robust findings were an increase in cerebral glucose metabolism in the right precentral gyrus and a decrease in the left superior temporal gyrus, left middle temporal gyrus, and cerebellum. Additionally, the sex distribution and illness duration had significant moderating effects on cerebral glucose metabolism alterations. CONCLUSIONS: Cerebral glucose metabolism alterations in these brain regions are likely to reflect the disease‐related functional abnormalities such as emotion and cognition. These findings contribute to a better understanding of the neurobiological underpinnings of bipolar disorder. Limitations. This study was done at a study level and cannot be addressed at the patient level. Subgroup analysis of BD I and BD II is not possible due to limited literature data. John Wiley and Sons Inc. 2021-03-26 /pmc/articles/PMC8119802/ /pubmed/33769704 http://dx.doi.org/10.1002/brb3.2117 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Research
Wu, Chujun
Ren, Chutong
Teng, Ziwei
Li, Sujuan
Silva, Floyd
Wu, Haishan
Chen, Jindong
Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies
title Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies
title_full Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies
title_fullStr Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies
title_full_unstemmed Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies
title_short Cerebral glucose metabolism in bipolar disorder: A voxel‐based meta‐analysis of positron emission tomography studies
title_sort cerebral glucose metabolism in bipolar disorder: a voxel‐based meta‐analysis of positron emission tomography studies
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119802/
https://www.ncbi.nlm.nih.gov/pubmed/33769704
http://dx.doi.org/10.1002/brb3.2117
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