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Abnormal functional connectivity within the prefrontal cortex is associated with multiple plasma lipid species in major depressive disorder

重性抑郁障碍 前额叶皮质 双相情感障碍 功能磁共振成像 额上回 病理生理学 神经科学 内科学 心理学 脂类学 化学 医学 生物化学 认知
作者
Jinxue Wei,Zijian Zhang,Xiao Yang,Liansheng Zhao,Min Wang,Yikai Dou,Yushun Yan,Rong‐Jun Ni,Meng Gong,Zaiquan Dong,Xiaohong Ma
出处
期刊:Journal of Affective Disorders [Elsevier]
卷期号:350: 713-720 被引量:3
标识
DOI:10.1016/j.jad.2023.12.072
摘要

Abnormalities in functional connectivity (FC) in major depressive disorder (MDD) have been widely reported. Analysis of the relationship between FC and plasma lipid profiles would be meaningful in the exploration of pathophysiological mechanisms and helpful for the identification of biomarkers for MDD. Patients with MDD (n = 49) and healthy controls (HC, n = 87) were recruited. Resting-state functional magnetic resonance imaging (rs-fMRI) data were collected for FC construction. The plasma lipid profiles were acquired using ultra-performance liquid chromatography (UPLC) and mass spectrometry (MS) analysis and clustered as co-expression modules. The differential FC and lipid modules between HCs and patients with MDD were identified, and then the association between FC and lipid co-expression modules was analyzed using correlation analysis. The modules associated molecular function was explored using metabolite set enrichment analysis (MSEA). MDD-associated FC and lipid co-expression modules were identified. One module was associated with FC values between the right orbital part of the middle frontal gyrus and the opercular part of the left inferior frontal gyrus, which was enriched in lipid sets of diacylglycerols and fatty alcohols; another module was associated with FC values between the right middle frontal gyrus and the right anterior cingulate and paracingulate gyri, which was enriched in lipid sets of glycerophosphocholines and glycerophosphoethanolamines. Our results indicated that abnormal FC in the prefrontal cortex is associated with multiple plasma lipid species, which may provide novel clues for exploring the pathophysiology of MDD.
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