Translational Addiction Research Laboratory, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON M5S 2S1, Canada.
Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada.
Int J Mol Sci. 2022 Apr 26;23(9):4754. doi: 10.3390/ijms23094754.
(1) Objective: Considering that current knowledge of mechanisms involved in the molecular pathogenesis of Social Anxiety Disorder (SAD) is limited, we conducted a systematic review to evaluate cumulative data obtained by Proton Magnetic Resonance Spectroscopic (H MRS) studies. (2) Methods: A computer-based literature search of Medline, EMBASE, PsycInfo, and ProQuest was performed. Only cross-sectional studies using H MRS techniques in participants with SAD and healthy controls (HCs) were selected. (3) Results: The search generated eight studies. The results indicated regional abnormalities in the 'fear neurocircuitry' in patients with SAD. The implicated regions included the anterior cingulate cortex (ACC), dorsomedial prefrontal cortex (dmPFC), dorsolateral prefrontal cortex (dlPFC), insula, occipital cortex (OC), as well as the subcortical regions, including the thalamus, caudate, and the putamen. (4) Conclusions: The evidence derived from eight studies suggests that possible pathophysiological mechanisms of SAD include impairments in the integrity and function of neurons and glial cells, including disturbances in energy metabolism, maintenance of phospholipid membranes, dysregulations of second messenger systems, and excitatory/inhibitory neurocircuitry. Conducting more cross-sectional studies with larger sample sizes is warranted given the limited evidence in this area of research.
(1) 目的:鉴于目前对社交焦虑障碍(SAD)分子发病机制中涉及的机制的了解有限,我们进行了系统评价,以评估质子磁共振波谱(H MRS)研究获得的累积数据。(2) 方法:计算机检索 Medline、EMBASE、PsycInfo 和 ProQuest 中的文献。仅选择了在 SAD 患者和健康对照者(HCs)中使用 H MRS 技术的横断面研究。(3) 结果:搜索生成了八项研究。结果表明,SAD 患者的“恐惧神经回路”存在区域性异常。涉及的区域包括前扣带回皮质(ACC)、背内侧前额叶皮质(dmPFC)、背外侧前额叶皮质(dlPFC)、岛叶、枕叶皮质(OC)以及包括丘脑、尾状核和壳核在内的皮质下区域。(4) 结论:八项研究的证据表明,SAD 的可能病理生理机制包括神经元和神经胶质细胞的完整性和功能受损,包括能量代谢紊乱、磷脂膜的维持、第二信使系统的失调以及兴奋性/抑制性神经回路。鉴于该研究领域的证据有限,进行更多具有更大样本量的横断面研究是有必要的。