Panagiotidis P, Kaprinis G, Iacovides A, Fountoulakis K
Psychiatric clinic, 424 General Military Hospital of Thessaloniki.
Medical School, Aristotle University of Thessaloniki.
Psychiatriki. 2013 Oct-Dec;24(4):272-87.
Though the pathobiology of schizophrenia can be examined in multiple levels, the organic notion of brain disease suggests that neurological features will be present. One straightforward, inexpensive method of investigating brain dysfunction in schizophrenia is thought the bedside assessment of neurological abnormalities with a standard neurological examination. Neurological abnormalities are traditionally classified as "hard signs" (impairments in basic motor, sensory, and reflex behaviors, which do not appear to be affected in schizophrenia) and "soft signs", which refer to more complex phenomena such as abnormalities in motor control, integrative sensory function, sensorimotor integration, and cerebral laterality. Additionally, neurological soft signs (NSS) are minor motor and sensory abnormalities that are considered to be normal in the course of early development but abnormal when elicited in later life or persist beyond childhood. Soft signs also, have no definitive localizing significance but are indicative of subtle brain dysfunction. Most authors believe that they are a reflection not only of deficient integration between the sensory and motor systems, but also of dysfunctional neuronal circuits linking subcortical brain structures such as the basal ganglia, the brain stem, and the limbic system. Throughout the last four decades, studies have consistently shown that NSS are more frequently present in patients with schizophrenia than in normal subjects and non-psychotic psychiatric patients. However, the functional relevance of NSS remains unclear and their specificity has often been challenged, even though there is indication for a relative specificity with regard to diagnosis, or symptomatology. Many studies have considered soft signs as categorical variables thus hampering the evaluation of fluctuation with symptomatology and/or treatment, whereas other studies included insufficient number of assessed signs, or lacked a comprehensive assessment of extrapyramidal symptomatology. Factors such as sex, age or family history of schizophrenia, are said to influence the performance of neurological examination, whereas relative few studies have provided longitudinal follow-up data on neurological soft signs in a sufficient number of patients, in order to address a possible deterioration of neurological functions. Finally, one additional difficulty when analyzing the NSS literature lies in the diversity of symptoms that are evaluated in the studies and/or non-standardized procedures or scoring. We will review some basic issues concerning recurrent difficulties in the measurement and definition of soft signs, as well as controversies on the significance of these signs with respect to clinical subtyping of schizophrenia, and social and demographic variables.
尽管精神分裂症的病理生物学可以在多个层面进行研究,但脑部疾病的器质性概念表明其会存在神经学特征。一种直接且经济的研究精神分裂症脑功能障碍的方法是通过标准神经学检查在床边评估神经学异常情况。神经学异常传统上分为“硬体征”(基本运动、感觉和反射行为的损害,在精神分裂症中似乎不受影响)和“软体征”,软体征指更复杂的现象,如运动控制异常、综合感觉功能异常、感觉运动整合异常和大脑半球优势异常。此外,神经学软体征(NSS)是轻微的运动和感觉异常,在早期发育过程中被认为是正常的,但在成年后引出或持续到童年之后则被视为异常。软体征也没有明确的定位意义,但表明存在细微的脑功能障碍。大多数作者认为,它们不仅反映了感觉和运动系统之间整合不足,还反映了连接基底神经节、脑干和边缘系统等皮质下脑结构的神经元回路功能失调。在过去的四十年里,研究一直表明,精神分裂症患者比正常受试者和非精神病性精神科患者更频繁地出现神经学软体征。然而,神经学软体征的功能相关性仍不明确,其特异性也经常受到质疑,尽管有迹象表明其在诊断或症状学方面具有相对特异性。许多研究将软体征视为分类变量,从而妨碍了对症状和/或治疗波动的评估,而其他研究评估的体征数量不足,或缺乏对锥体外系症状的全面评估。据说,性别、年龄或精神分裂症家族史等因素会影响神经学检查的结果,而相对较少的研究为足够数量的患者提供了神经学软体征的纵向随访数据,以探讨神经功能可能的恶化情况。最后,分析神经学软体征文献时的另一个困难在于研究中评估的症状多样性以及非标准化程序或评分。我们将回顾一些基本问题,这些问题涉及软体征测量和定义中反复出现的困难,以及这些体征在精神分裂症临床亚型分类以及社会和人口统计学变量方面的意义争议。