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痴呆症中神经精神综合征的神经生物学

The neurobiology of neuropsychiatric syndromes in dementia.

作者信息

Meeks Thomas W, Ropacki Susan A, Jeste Dilip V

机构信息

Division of Geriatric Psychiatry, Department of Psychiatry, University of California, San Diego, and Veterans Affairs San Diego Healthcare System, San Diego, California 92161, USA.

出版信息

Curr Opin Psychiatry. 2006 Nov;19(6):581-6. doi: 10.1097/01.yco.0000245746.45384.0e.

DOI:10.1097/01.yco.0000245746.45384.0e
PMID:17012935
Abstract

PURPOSE OF REVIEW

Neuropsychiatric disturbances in dementia are prevalent, and research is uncovering their neurobiological correlates.

RECENT FINDINGS

Late-onset depression appears to be associated with Alzheimer's disease pathology at autopsy, and lifetime depression episodes may worsen Alzheimer's disease pathology in the hippocampus. Vascular disease and elevated homocysteine increase risk for both late-onset depression and Alzheimer's disease and may partly mediate their relationship. Monoamine changes are robust finding in Alzheimer's disease and may account for many observed depression symptoms. Risk of psychosis of Alzheimer's disease appears to be increased by several genes also implicated in schizophrenia (e.g., catechol-O-methyltransferase, neuregulin-1). Psychosis in dementia with Lewy bodies appears to be related to cholinergic deficits. Alzheimer's disease is associated with changes in the circadian sleep-wake cycles, including decreased night-time melatonin. Sleep apnea may be related to apolipoprotein E genotype and impact cognition in Alzheimer's disease. Rapid eye movement sleep behavior disorder is intricately related to synucleinopathies, such as dementia with Lewy bodies, but synuclein changes may not totally explain this relationship.

SUMMARY

Neuropsychiatric disturbances are a core feature of dementia and worsen many clinical outcomes. Among the most validated syndromes are depression, psychosis, and sleep disturbance of Alzheimer's disease. Neuropathology, neuroimaging, and genetic studies increasingly provide insight into the origins of these psychiatric symptoms in dementia.

摘要

综述目的

痴呆中的神经精神障碍很常见,研究正在揭示其神经生物学相关性。

最新发现

尸检时迟发性抑郁症似乎与阿尔茨海默病病理相关,一生中的抑郁发作可能会使海马体中的阿尔茨海默病病理恶化。血管疾病和高同型半胱氨酸血症会增加迟发性抑郁症和阿尔茨海默病的风险,并可能部分介导它们之间的关系。单胺变化是阿尔茨海默病中一个有力的发现,可能解释许多观察到的抑郁症状。阿尔茨海默病的精神病风险似乎因一些也与精神分裂症有关的基因(如儿茶酚-O-甲基转移酶、神经调节蛋白-1)而增加。路易体痴呆中的精神病似乎与胆碱能缺陷有关。阿尔茨海默病与昼夜睡眠-觉醒周期的变化有关,包括夜间褪黑素减少。睡眠呼吸暂停可能与载脂蛋白E基因型有关,并影响阿尔茨海默病的认知。快速眼动睡眠行为障碍与突触核蛋白病密切相关,如路易体痴呆,但突触核蛋白的变化可能无法完全解释这种关系。

总结

神经精神障碍是痴呆的核心特征,并会使许多临床结局恶化。在最得到验证的综合征中包括阿尔茨海默病的抑郁、精神病和睡眠障碍。神经病理学、神经影像学和遗传学研究越来越多地为痴呆中这些精神症状的起源提供见解。

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