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精神分裂症的渐进性变化:它们是否存在以及意味着什么?

Progressive changes in schizophrenia: do they exist and what do they mean?

作者信息

Anderson J E, O'Donnell B F, McCarley R W, Shenton M E

机构信息

The Clinical Neuroscience Division, Laboratory of Neuroscience, Department of Psychiatry, Brockton VA Medical Centre and Harvard Medical School, Boston, MA 02401, USA.

出版信息

Restor Neurol Neurosci. 1998 Jun;12(2-3):175-84.

Abstract

Schizophrenia is a disorder characterized by multiple symptoms, with a varied course and outcome. The etiology is yet unknown, but multiple pathological processes or, equally likely, a unique pathophysiological process, may be involved. Here, we review evidence for progressive changes in schizophrenia in order to understand further the pathophysiology of this disorder. We first present evidence for clinical and psycho-social changes over time, followed by evidence from structural brain studies that suggests that schizophrenia is a brain disorder. We then review findings from the small number of longitudinal studies that have evaluated structural brain changes in schizophrenia, followed by a review of the evidence for neurophysiological changes, both cross-sectional and longitudinal. This is followed by a discussion of possible cellular mechanisms, including NMDA receptor abnormalities, that might account for structural and functional brain changes (temporal and frontal), and we discuss how these abnormalities might be related to not only the specific signs and symptoms of schizophrenia but also to the onset and course of the illness. Finally, we discuss neurodevelopment (static and perhaps non-static alterations) and neurodegenerative theories of schizophrenia. We propose that the two are not mutually exclusive, but instead likely reflect a "two-hit" model for some subtypes of schizophrenia.

摘要

精神分裂症是一种具有多种症状、病程和结局各异的疾病。其病因尚不清楚,但可能涉及多种病理过程,或者同样可能涉及一种独特的病理生理过程。在此,我们回顾精神分裂症进行性变化的证据,以便进一步了解该疾病的病理生理学。我们首先呈现随时间推移临床和心理社会变化的证据,接着是来自脑结构研究的证据,这些证据表明精神分裂症是一种脑部疾病。然后我们回顾少数评估精神分裂症脑结构变化的纵向研究结果,随后是对横断面和纵向神经生理变化证据的综述。接下来讨论可能的细胞机制,包括N-甲基-D-天冬氨酸(NMDA)受体异常,这些机制可能解释脑结构和功能变化(颞叶和额叶),并且我们讨论这些异常如何不仅与精神分裂症的特定体征和症状相关,还与疾病的发作和病程相关。最后,我们讨论精神分裂症的神经发育(静态以及可能的非静态改变)和神经退行性理论。我们提出这两者并非相互排斥,而是可能反映了某些精神分裂症亚型的“两次打击”模型。

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