Department of Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.
Department of Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.
Schizophr Res. 2014 Jan;152(1):73-80. doi: 10.1016/j.schres.2013.07.038. Epub 2013 Aug 6.
Self-disturbances (SDs) are increasingly identified in schizophrenia and are theorized to confer vulnerability to psychosis. Neuroimaging research has shed some light on the neural correlates of SDs in schizophrenia. But, the onset and trajectory of the neural alterations underlying SDs in schizophrenia remain incompletely understood. We hypothesize that the aberrant structure and function of brain areas (e.g., prefrontal, lateral temporal, and parietal cortical structures) comprising the "neural circuitry of self" may represent an early, premorbid (i.e., pre-prodromal) indicator of schizophrenia risk. Consistent with neurodevelopmental models, we argue that "early" (i.e., perinatal) dysmaturational processes (e.g., abnormal cortical neural cell migration and mini-columnar formation) affecting key prefrontal (e.g., medial prefrontal cortex), lateral temporal cortical (e.g., superior temporal sulcus), and parietal (e.g., inferior parietal lobule) structures involved in self-processing may lead to subtle disruptions of "self" during childhood in persons at risk for schizophrenia. During adolescence, progressive neurodevelopmental alterations (e.g., aberrant synaptic pruning) affecting the neural circuitry of self may contribute to worsening of SDs. This could result in the emergence of prodromal symptoms and, eventually, full-blown psychosis. To highlight why adolescence may be a period of heightened risk for SDs, we first summarize the literature regarding the neural correlates of self in typically developing children. Next, we present evidence from neuroimaging studies in genetic high-risk youth suggesting that fronto-temporal-parietal structures mediating self-reflection may be abnormal in the premorbid period. Our goal is that the ideas presented here might provide future directions for research into the neurobiology of SDs during the pre-psychosis development of youth at risk for schizophrenia.
自我扰动(SDs)在精神分裂症中越来越多地被识别出来,并被认为是易患精神病的因素。神经影像学研究揭示了精神分裂症中 SD 的神经相关性。但是,SD 所涉及的神经改变的起始和轨迹仍然不完全清楚。我们假设,构成“自我神经回路”的大脑区域(例如前额叶、外侧颞叶和顶叶皮质结构)的异常结构和功能可能代表精神分裂症风险的早期、前驱(即前驱期)指标。与神经发育模型一致,我们认为“早期”(即围产期)发育不良过程(例如皮质神经细胞迁移和迷你柱状形成异常)影响关键的前额叶(例如内侧前额叶皮质)、外侧颞叶皮质(例如颞上沟)和顶叶(例如顶下小叶)与自我加工相关的结构,可能导致处于精神分裂症风险中的个体在儿童期出现“自我”的细微破坏。在青春期,影响自我神经回路的进行性神经发育改变(例如异常的突触修剪)可能会导致 SD 的恶化。这可能导致前驱症状的出现,并最终导致完全精神病发作。为了强调为什么青春期可能是 SD 风险增加的时期,我们首先总结了关于典型发展儿童自我神经相关性的文献。接下来,我们介绍了来自遗传高风险青年神经影像学研究的证据,表明介导自我反思的额颞顶叶结构在前驱期可能异常。我们的目标是,这里提出的观点可能为研究处于前驱期的精神分裂症高危青年的 SD 神经生物学提供未来的方向。