Key Laboratory for NeuroInformation of Ministry of Education, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054, PR China.
Brain Res. 2011 May 4;1388:167-77. doi: 10.1016/j.brainres.2011.03.018. Epub 2011 Mar 12.
In social anxiety disorder (SAD), impairments in limbic/paralimbic structures are associated with emotional dysregulation and inhibition of the medial prefrontal cortex (MPFC). Little is known, however, about alterations in limbic and frontal regions associated with the integrated morphometric, functional, and structural architecture of SAD. Whether altered gray matter volume is associated with altered functional and structural connectivity in SAD. Three techniques were used with 18 SAD patients and 18 healthy controls: voxel-based morphometry; resting-state functional connectivity analysis; and diffusion tensor imaging tractography. SAD patients exhibited significantly decreased gray matter volumes in the right posterior inferior temporal gyrus (ITG) and right parahippocampal/hippocampal gyrus (PHG/HIP). Gray matter volumes in these two regions negatively correlated with the fear factor of the Liebowitz Social Anxiety Scale. In addition, we found increased functional connectivity in SAD patients between the right posterior ITG and the left inferior occipital gyrus, and between the right PHF/HIP and left middle temporal gyrus. SAD patients had increased right MPFC volume, along with enhanced structural connectivity in the genu of the corpus callosum. Reduced limbic/paralimbic volume, together with increased resting-state functional connectivity, suggests the existence of a compensatory mechanism in SAD. Increased MPFC volume, consonant with enhanced structural connectivity, suggests a long-time overgeneralization of structural connectivity and a role of this area in the mediation of clinical severity. Overall, our results may provide a valuable basis for future studies combining morphometric, functional and anatomical data in the search for a comprehensive understanding of the neural circuitry underlying SAD.
在社交焦虑障碍(SAD)中,边缘/旁边缘结构的损伤与情绪调节障碍和内侧前额叶皮质(MPFC)的抑制有关。然而,关于与 SAD 的综合形态、功能和结构架构相关的边缘和额叶区域的改变知之甚少。改变的灰质体积是否与 SAD 中的功能和结构连接改变有关。使用三种技术对 18 名 SAD 患者和 18 名健康对照组进行了研究:体素形态测量学;静息状态功能连接分析;和弥散张量成像追踪。SAD 患者右侧后颞下回(ITG)和右侧海马旁回/海马回(PHG/HIP)的灰质体积显著减少。这两个区域的灰质体积与 Liebowitz 社交焦虑量表的恐惧因子呈负相关。此外,我们发现 SAD 患者右侧后 ITG 与左侧下枕叶之间以及右侧 PHF/HIP 与左侧颞中回之间的功能连接增加。SAD 患者右侧 MPFC 体积增加,胼胝体膝部结构连接增强。边缘/旁边缘区域的灰质体积减少,与静息状态功能连接增加,提示 SAD 中存在代偿机制。MPFC 体积增加,与结构连接增强一致,提示结构连接的长时间过度泛化以及该区域在调节临床严重程度中的作用。总的来说,我们的结果可能为未来的研究提供有价值的基础,这些研究将形态学、功能和解剖学数据结合起来,以全面了解 SAD 下的神经回路。