Inflammation is correlated with abnormal functional connectivity in unmedicated bipolar depression: an independent component analysis study of resting-state fMRI

中央前回 静息状态功能磁共振成像 炎症 眶额皮质 内科学 功能磁共振成像 萧条(经济学) 神经科学 内分泌学 心理学 医学 双相情感障碍 磁共振成像 精神科 认知 前额叶皮质 宏观经济学 锂(药物) 经济 放射科
作者
Guixian Tang,Pan Chen,Guanmao Chen,Shuming Zhong,Jiaying Gong,Hui Zhong,Tao Ye,Feng Chen,Jurong Wang,Zhenye Luo,Zhangzhang Qi,Yanbin Jia,Ying Wang,Li Huang
出处
期刊:Psychological Medicine [Cambridge University Press]
卷期号:52 (15): 3431-3441 被引量:34
标识
DOI:10.1017/s003329172100009x
摘要

Abstract Background Inflammation might play a role in bipolar disorder (BD), but it remains unclear the relationship between inflammation and brain structural and functional abnormalities in patients with BD. In this study, we focused on the alterations of functional connectivity (FC), peripheral pro-inflammatory cytokines and their correlations to investigate the role of inflammation in FC in BD depression. Methods In this study, 42 unmedicated patients with BD II depression and 62 healthy controls (HCs) were enrolled. Resting-state-functional magnetic resonance imaging was performed in all participants and independent component analysis was used. Serum levels of Interleukin-6 (IL-6) and Interleukin-8 (IL-8) were measured in all participants. Correlation between FC values and IL-6 and IL-8 levels in BD was calculated. Results Compared with the HCs, BD II patients showed decreased FC in the left orbitofrontal cortex (OFC) implicating the limbic network and the right precentral gyrus implicating the somatomotor network. BD II showed increased IL-6 ( p = 0.039), IL-8 ( p = 0.002) levels. Moreover, abnormal FC in the right precentral gyrus were inversely correlated with the IL-8 ( r = −0.458, p = 0.004) levels in BD II. No significant correlation was found between FC in the left OFC and cytokines levels. Conclusions Our findings that serum IL-8 levels are associated with impaired FC in the right precentral gyrus in BD II patients suggest that inflammation might play a crucial role in brain functional abnormalities in BD.
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