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Associations of leptin and corticostriatal connectivity in bipolar disorder

Bipolar disorder (BD) and metabolic disturbance represent a chronic state of low-grade inflammation and corticostriatal circuitry alterations. Herein, we aimed to investigate whether plasma leptin, an adipokine that plays a key role in the interplay of metabolism and inflammation, is associated with...

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Autores principales: Wei, Shyh-Yuh, Tseng, Huai-Hsuan, Chang, Hui Hua, Chang, Wei Hung, Yang, Yen Kuang, Chen, Po See
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763246/
https://www.ncbi.nlm.nih.gov/pubmed/36535988
http://dx.doi.org/10.1038/s41598-022-26233-8
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author Wei, Shyh-Yuh
Tseng, Huai-Hsuan
Chang, Hui Hua
Chang, Wei Hung
Yang, Yen Kuang
Chen, Po See
author_facet Wei, Shyh-Yuh
Tseng, Huai-Hsuan
Chang, Hui Hua
Chang, Wei Hung
Yang, Yen Kuang
Chen, Po See
author_sort Wei, Shyh-Yuh
collection PubMed
description Bipolar disorder (BD) and metabolic disturbance represent a chronic state of low-grade inflammation and corticostriatal circuitry alterations. Herein, we aimed to investigate whether plasma leptin, an adipokine that plays a key role in the interplay of metabolism and inflammation, is associated with corticostriatal connectivity in patients with BD. Twenty-eight BD I patients, 36 BD II patients and 66 healthy controls were enrolled and completed the Hamilton Depression Rating Scale, the Young Mania Rating Scale, and the Recent Life Change Questionnaire. Fasting plasma leptin and C-reactive protein (CRP) levels were measured, and corticostriatal connectivity was examined using functional magnetic resonance imaging (fMRI). The relationships between leptin, CRP and body mass index (BMI) identified in the controls and BD II patients were absent in the BD I patients. We did not find a significant group difference in the leptin level; nevertheless, the negative correlation between leptin level and corticostriatal connectivity (ventrolateral prefrontal cortex and inferior temporal gyrus) observed in the healthy controls was absent in the BD patients. The disproportionate increase in leptin level with increasing BMI in BD indicated a potential inflammatory role of white adipose tissue in BD. Furthermore, higher CRP levels in BD I patients might induce leptin resistance. Collectively, our results implied vulnerability to inflammatory and metabolic diseases in patients with BD, especially BD I.
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spelling pubmed-97632462022-12-21 Associations of leptin and corticostriatal connectivity in bipolar disorder Wei, Shyh-Yuh Tseng, Huai-Hsuan Chang, Hui Hua Chang, Wei Hung Yang, Yen Kuang Chen, Po See Sci Rep Article Bipolar disorder (BD) and metabolic disturbance represent a chronic state of low-grade inflammation and corticostriatal circuitry alterations. Herein, we aimed to investigate whether plasma leptin, an adipokine that plays a key role in the interplay of metabolism and inflammation, is associated with corticostriatal connectivity in patients with BD. Twenty-eight BD I patients, 36 BD II patients and 66 healthy controls were enrolled and completed the Hamilton Depression Rating Scale, the Young Mania Rating Scale, and the Recent Life Change Questionnaire. Fasting plasma leptin and C-reactive protein (CRP) levels were measured, and corticostriatal connectivity was examined using functional magnetic resonance imaging (fMRI). The relationships between leptin, CRP and body mass index (BMI) identified in the controls and BD II patients were absent in the BD I patients. We did not find a significant group difference in the leptin level; nevertheless, the negative correlation between leptin level and corticostriatal connectivity (ventrolateral prefrontal cortex and inferior temporal gyrus) observed in the healthy controls was absent in the BD patients. The disproportionate increase in leptin level with increasing BMI in BD indicated a potential inflammatory role of white adipose tissue in BD. Furthermore, higher CRP levels in BD I patients might induce leptin resistance. Collectively, our results implied vulnerability to inflammatory and metabolic diseases in patients with BD, especially BD I. Nature Publishing Group UK 2022-12-19 /pmc/articles/PMC9763246/ /pubmed/36535988 http://dx.doi.org/10.1038/s41598-022-26233-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wei, Shyh-Yuh
Tseng, Huai-Hsuan
Chang, Hui Hua
Chang, Wei Hung
Yang, Yen Kuang
Chen, Po See
Associations of leptin and corticostriatal connectivity in bipolar disorder
title Associations of leptin and corticostriatal connectivity in bipolar disorder
title_full Associations of leptin and corticostriatal connectivity in bipolar disorder
title_fullStr Associations of leptin and corticostriatal connectivity in bipolar disorder
title_full_unstemmed Associations of leptin and corticostriatal connectivity in bipolar disorder
title_short Associations of leptin and corticostriatal connectivity in bipolar disorder
title_sort associations of leptin and corticostriatal connectivity in bipolar disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763246/
https://www.ncbi.nlm.nih.gov/pubmed/36535988
http://dx.doi.org/10.1038/s41598-022-26233-8
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