Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University Mannheim, Germany.
Center for Psychosocial Medicine, Department of General Psychiatry, University of Heidelberg, Germany.
Schizophr Res. 2018 Oct;200:26-34. doi: 10.1016/j.schres.2017.10.007. Epub 2017 Nov 1.
Primary motor abnormalities (PMA), as found in patients with schizophrenia, are quantitatively and qualitatively distinct markers of motor system abnormalities. PMA have been often referred to phenomena that are present across schizophrenia-spectrum disorders. A dysfunction of frontoparietal and subcortical networks has been proposed as core pathophysiological mechanism underlying the expression of PMA. However, it is unclear at present if such mechanisms are a common within schizophrenia and other psychotic disorders. To address this question, we review recent neuroimaging studies investigating the neural substrates of PMA in schizophrenia and so-called "nonschizophrenic nonaffective psychoses" (NSNAP) such as schizophreniform, schizoaffective, brief psychotic, and other unspecified psychotic disorders. Although the extant data in patients with schizophrenia suggests that further investigation is warranted, MRI findings in NSNAP are less persuasive. It is unclear so far which PMA, if any, are characteristic features of NSNAP or, possibly even specific for these disorders. Preliminary data suggest a relationship between relapsing-remitting PMA in hyper-/hypokinetic cycloid syndromes and neurodegenerative disorders of the basal ganglia, likely reflecting the transnosological relevance of subcortical abnormalities. Despite this evidence, neural substrates and mechanisms underlying PMA that are common in schizophrenia and NSNAP cannot be clearly delineated at this stage of research. PMA and their underlying brain circuits could be promising intermediate phenotype candidates for psychotic disorders, but future multimodal neuroimaging studies in schizophrenia and NSNAP patients and their unaffected first-degree relatives are needed to answer fundamental transnosologic questions.
原发性运动异常(PMA)在精神分裂症患者中被发现,是运动系统异常的定量和定性的明显标志物。PMA 通常被称为存在于精神分裂症谱系障碍中的现象。 前额顶叶和皮质下网络功能障碍被认为是 PMA 表达的核心病理生理机制。然而,目前尚不清楚这种机制在精神分裂症和其他精神病障碍中是否普遍存在。为了解决这个问题,我们回顾了最近的神经影像学研究,这些研究调查了精神分裂症和所谓的“非精神分裂症非情感性精神病”(NSNAP)中 PMA 的神经基础,如分裂型、分裂情感性、短暂性精神病和其他未指定的精神病障碍。尽管精神分裂症患者的现有数据表明需要进一步研究,但 NSNAP 的 MRI 发现不太有说服力。到目前为止,还不清楚哪些 PMA(如果有的话)是 NSNAP 的特征特征,甚至可能是这些疾病的特异性特征。初步数据表明,在高/低动力周期性综合征中的复发性 PMA 与基底节的神经退行性疾病之间存在关系,这可能反映了皮质下异常的跨疾病相关性。尽管有这些证据,但在现阶段的研究中,尚不能清楚地区分精神分裂症和 NSNAP 中常见的 PMA 及其潜在的大脑回路的神经基础和机制。PMA 及其潜在的大脑回路可能是精神病的有前途的中间表型候选者,但需要对精神分裂症和 NSNAP 患者及其未受影响的一级亲属进行未来的多模态神经影像学研究,以回答基本的跨疾病问题。