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迟发性精神分裂症和极晚发性精神分裂症样精神病的神经心理学和神经生物学:批判性综述。

The neuropsychology and neurobiology of late-onset schizophrenia and very-late-onset schizophrenia-like psychosis: A critical review.

机构信息

Section of Old Age Psychiatry, Department of Psychiatry, University Hospitals Leuven, KUL, Belgium.

Collaborative Antwerp Psychiatric Research Institute (CAPRI), University of Antwerp, Antwerp, Belgium; University Psychiatric Hospital Antwerp, Campus Duffel, Belgium.

出版信息

Neurosci Biobehav Rev. 2017 Dec;83:604-621. doi: 10.1016/j.neubiorev.2017.08.024. Epub 2017 Sep 1.

Abstract

OBJECTIVE

The current review discusses neuropsychological profiles and the longitudinal course of cognitive dysfunction in Late Onset Schizophrenia (LOS) and Very-late-onset schizophrenia-like psychosis (VLOSLP), and attempts to clarify its neurobiological underpinnings.

METHOD

A systematic literature search resulted in 29 publications describing original research on the neuropsychology of LOS/VLOSLP and 46 studies focussing on neurobiology.

RESULTS

Although mildly progressive cognitive impairment is usually present, only a subgroup of LOS/VLOSLP develops dementia during a 10-year follow-up succeeding the onset of psychosis. This coincides with the absence of neuropathological evidence for neurodegeneration in many cases. Cognitive deterioration is characterized by deficits in (working) memory, language, psychomotor speed and executive functioning. Underlying neurobiological changes encompass white matter pathology, increased ventricle-to-brain ratio (VBR) with coinciding atrophy and hypo-metabolism of frontal, temporal and subcortical areas.

CONCLUSIONS

Multiple changes in neurobiology and cognition contributing to LOS/VLOSLP may reflect stress-related accelerated brain aging rather than neurodegenerative pathology. Their involvement in the onset of illness, however, might be inversely proportional to pre-existing (psychosocial and/or genetic) vulnerability to psychosis.

摘要

目的

本综述讨论了晚发性精神分裂症(LOS)和极晚发性类似精神分裂症的精神病(VLOSLP)的神经心理学特征和认知功能障碍的纵向病程,并试图阐明其神经生物学基础。

方法

系统文献检索产生了 29 篇描述 LOS/VLOSLP 神经心理学的原始研究和 46 篇专注于神经生物学的研究。

结果

尽管通常存在轻度进行性认知障碍,但只有一小部分 LOS/VLOSLP 在精神病发作后 10 年的随访中发展为痴呆。这与许多情况下没有神经病理学证据表明神经退行性变相吻合。认知恶化的特征是(工作)记忆、语言、精神运动速度和执行功能缺陷。潜在的神经生物学变化包括白质病理学、脑室-脑比率(VBR)增加伴有相应的额叶、颞叶和皮质下区域的萎缩和低代谢。

结论

导致 LOS/VLOSLP 的神经生物学和认知的多种变化可能反映了与应激相关的加速脑老化,而不是神经退行性病理。然而,它们与疾病的发生之间的关系可能与精神病的先前存在的(心理社会和/或遗传)易感性成反比。

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