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痴呆患者嗅觉通路中的α-突触核蛋白病变

Alpha-synuclein pathology in the olfactory pathways of dementia patients.

作者信息

Hubbard Paul S, Esiri Margaret M, Reading Margaret, McShane Rupert, Nagy Zsuzsanna

机构信息

Division of Neuroscience, The Medical School, University of Birmingham, UK.

出版信息

J Anat. 2007 Jul;211(1):117-24. doi: 10.1111/j.1469-7580.2007.00748.x. Epub 2007 Jun 6.

Abstract

Lewy-type pathology is a characteristic of a number of neurodegenerative disorders, including Parkinson's disease and dementia with Lewy bodies. Thus far, the definitive diagnosis of these dementias can only be confirmed at post-mortem. However, it is known that the loss of smell (anosmia) is an early symptom in patients who develop dementia, and the use of the smell test has been proposed as an early diagnostic procedure. The aim of this study was to understand further the extent of Lewy pathology in the olfactory system of patients with neurodegenerative disorders. Post-mortem tissue from 250 subjects was obtained from the OPTIMA brain bank. Five areas of the olfactory pathway were examined by immunolabelling for alpha-synuclein - a major component of Lewy pathology: the olfactory tract/bulb (n = 79), the anterior olfactory nucleus in the lateral olfactory gyrus (n = 193), the region of olfactory projection to the orbito-frontal cortex (n = 225), the hippocampus (n = 236) and the amygdala (n = 201). Results show that Lewy pathology affects different parts of the olfactory pathways differentially, suggesting a specific pattern of development of pathology. Clinical Parkinson's disease is most likely to be identified if the orbito-frontal cortex is affected, while the diagnosis is less likely if the pathology is restricted to the olfactory bulb or tract. These results suggest that pathology in the olfactory bulb and tract occurs prior to clinical signs of Parkinson's disease. Furthermore, the results presented here provide further evidence supporting the possible value of a smell test to aid the clinical diagnosis of neurodegenerative diseases.

摘要

路易体病理是包括帕金森病和路易体痴呆在内的多种神经退行性疾病的一个特征。到目前为止,这些痴呆症的确诊只能在尸检时得到证实。然而,已知嗅觉丧失(嗅觉减退)是痴呆症患者的早期症状,嗅觉测试已被提议作为一种早期诊断方法。本研究的目的是进一步了解神经退行性疾病患者嗅觉系统中路易体病理的程度。从OPTIMA脑库获取了250名受试者的尸检组织。通过对α-突触核蛋白(路易体病理的主要成分)进行免疫标记,检查了嗅觉通路的五个区域:嗅束/嗅球(n = 79)、外侧嗅回中的前嗅核(n = 193)、向眶额皮质的嗅觉投射区域(n = 225)、海马体(n = 236)和杏仁核(n = 201)。结果表明,路易体病理对嗅觉通路的不同部分影响不同,提示了一种特定的病理发展模式。如果眶额皮质受到影响,临床帕金森病最有可能被识别,而如果病理仅限于嗅球或嗅束,则诊断的可能性较小。这些结果表明,嗅球和嗅束中的病理在帕金森病的临床症状出现之前就已发生。此外,此处呈现的结果提供了进一步的证据,支持嗅觉测试在辅助神经退行性疾病临床诊断方面可能具有的价值。

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