Bender S, Weisbrod M, Resch F
Centre for Psychosocial Medicine, Department for Child and Adolescent Psychiatry, University of Heidelberg, Heidelberg, Germany.
J Neural Transm (Vienna). 2007 Sep;114(9):1199-215. doi: 10.1007/s00702-007-0742-4. Epub 2007 May 21.
The early recognition of schizophrenia seems crucial; various studies relate a longer duration-of-untreated-psychosis to a worse prognosis. We give an overview over common psychopathological early recognition instruments (BSABS, CAARMS, SIPS, IRAOS, ERIraos). However, many clinical symptoms of prodromal schizophrenia stages are not sufficiently specific. Thus we review recent contributions of neuroimaging and electrophysiological as well as genetic studies: which new diagnostic perspectives offer endophenotypes (such as P300, P50 sensory gating, MMN, smooth pursuit eye movements; indicating a specific genetic vulnerability) together with a better understanding of schizophrenic pathophysiology (state-dependent biological markers, e.g. aggravated motor neurological soft signs during psychosis) in prodromal schizophrenia when still ambiguous clinical symptoms are present. Several examples (e.g. from COMT polymorphisms to working memory deficits) illustrate more specific underlying neuronal mechanisms behind behavioural symptoms. This way, a characteristic pattern of disturbed cerebral maturation might be distinguished in order to complement clinical instruments of early schizophrenia detection.
精神分裂症的早期识别似乎至关重要;多项研究表明,未治疗精神病的持续时间越长,预后越差。我们概述了常见的精神病理学早期识别工具(简明精神症状评定量表、综合评估精神分裂症症状量表、精神分裂症前期症状评定量表、综合风险评估量表、简易精神分裂症风险评估量表)。然而,前驱期精神分裂症阶段的许多临床症状特异性不足。因此,我们回顾了神经影像学、电生理学以及遗传学研究的最新成果:当临床症状仍不明确时,哪些新的诊断视角提供了内表型(如P300、P50感觉门控、失匹负波、平稳跟踪眼球运动;表明特定的遗传易感性),同时加深了对前驱期精神分裂症病理生理学的理解(状态依赖性生物学标志物,如精神病发作时加重的运动神经软体征)。几个例子(如从儿茶酚-O-甲基转移酶基因多态性到工作记忆缺陷)说明了行为症状背后更具体的潜在神经元机制。通过这种方式,可能会区分出一种特征性的大脑成熟紊乱模式,以补充早期精神分裂症检测的临床工具。