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Peripheral Interleukin-18 is negatively correlated with abnormal brain activity in patients with depression: a resting-state fMRI study

BACKGROUND: Interleukin-18 (IL-18) may participate in the development of major depressive disorder, but the specific mechanism remains unclear. This study aimed to explore whether IL-18 correlates with areas of the brain associated with depression. METHODS: Using a case–control design, 68 subjects (...

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Detalles Bibliográficos
Autores principales: Du, Xiangdong, Zou, Siyun, Yue, Yan, Fang, Xiaojia, Wu, Yuxuan, Wu, Siqi, Wang, Haitao, Li, Zhe, Zhao, Xueli, Yin, Ming, Ye, Gang, Sun, Hongyan, Gu, Xiaochu, Zhang, Xiaobin, Miao, Zhigang, Jin, Jeff Wang, Wu, Hanjing Emily, Liu, Yansong, Xu, Xingshun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354267/
https://www.ncbi.nlm.nih.gov/pubmed/35931995
http://dx.doi.org/10.1186/s12888-022-04176-8
Descripción
Sumario:BACKGROUND: Interleukin-18 (IL-18) may participate in the development of major depressive disorder, but the specific mechanism remains unclear. This study aimed to explore whether IL-18 correlates with areas of the brain associated with depression. METHODS: Using a case–control design, 68 subjects (34 patients and 34 healthy controls) underwent clinical assessment, blood sampling, and resting-state functional Magnetic Resonance Imaging (fMRI). The total Hamilton depression-17 (HAMD-17) score was used to assess depression severity. Enzyme-linked immunosorbent assay (ELISA) was used to detect IL-18 levels. Rest-state fMRI was conducted to explore spontaneous brain activity. RESULTS: The level of IL-18 was higher in patients with depression in comparison with healthy controls. IL-18 was negatively correlated with degree centrality of the left posterior cingulate gyrus in the depression patient group, but no correlation was found in the healthy control group. CONCLUSION: This study suggests the involvement of IL-18 in the pathophysiological mechanism for depression and interference with brain activity.