Prasad Konasale M, Upton Catherine H, Nimgaonkar Vishwajit L, Keshavan Matcheri S
Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, United States.
Department of Psychiatry and Behavioral Neuroscience, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Schizophr Res. 2015 Jan;161(1):119-25. doi: 10.1016/j.schres.2014.09.043. Epub 2014 Oct 22.
The pathophysiological underpinnings of impaired anatomical and functional connectivity are not precisely known. Emerging data suggest that immune mediators may underlie such dysconnectivity. We examined anatomical brain connections using diffusion tensor imaging (DTI) data in relation to interleukin-6 (IL-6) and C-reactive protein (CRP) levels among early-course clinically stable schizophrenia subjects compared to healthy controls (HC).
DTI data were acquired in 30 directions with 2 averages. Fractional anisotropy (FA) and radial diffusivity (RD) maps were separately processed using FSL4.1.9 and Tract-Based Spatial Statistics (TBSS). Threshold free cluster enhancements (TFCE) were examined employing familywise error (FWE) corrections for multiple testing within linear regression models including age, sex and socioeconomic status as covariates. IL-6 and CRP were assayed using highly sensitive and specific sandwich immunosorbent assays.
The groups did not differ in age and sex as well as in the IL-6 and CRP levels. IL-6 levels were negatively correlated with the FA and positively correlated with RD among schizophrenia subjects but not HC. The voxel clusters that showed significant correlations were localized to the forceps major, the inferior longitudinal fasciculus and the inferior fronto-occipital fasciculus. CRP levels showed similar pattern except for lack of correlation with RD on any cluster that corresponded to the forceps major.
Our results suggest that the IL-6 and CRP contribute to impaired anisotropy of water diffusion in selected pathways that have been previously associated with schizophrenia suggesting differential susceptibility of selected neural pathways to immune mediators.
解剖学和功能连接受损的病理生理基础尚不完全清楚。新出现的数据表明,免疫介质可能是这种连接障碍的基础。我们使用扩散张量成像(DTI)数据,研究了早期病程临床稳定的精神分裂症患者与健康对照者(HC)之间,与白细胞介素-6(IL-6)和C反应蛋白(CRP)水平相关的脑解剖连接情况。
在30个方向上采集DTI数据,平均采集2次。使用FSL4.1.9和基于体素的空间统计学(TBSS)分别处理分数各向异性(FA)和径向扩散率(RD)图。在线性回归模型中,采用家族性错误(FWE)校正进行多重检验,以检查无阈值聚类增强(TFCE),该模型将年龄、性别和社会经济地位作为协变量。使用高灵敏度和特异性的夹心免疫吸附测定法检测IL-6和CRP。
两组在年龄、性别以及IL-6和CRP水平上没有差异。在精神分裂症患者中,IL-6水平与FA呈负相关,与RD呈正相关,但在HC中并非如此。显示出显著相关性的体素簇定位于主要钳状束、下纵束和下额枕束。CRP水平呈现出类似的模式,但在与主要钳状束对应的任何簇上,与RD均无相关性。
我们的结果表明,IL-6和CRP导致了先前与精神分裂症相关的特定通路中水扩散各向异性受损,这表明特定神经通路对免疫介质的易感性存在差异。