特发性帕金森病和弥漫性路易体病的局部脑萎缩。

K L Double, G M Halliday, D A McRitchie, W G Reid, M A Hely, J G Morris
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引用次数: 79

摘要

这项研究测量了特发性帕金森病和弥漫性路易体病患者的脑萎缩,所有这些患者都有相当程度的中脑多巴胺能神经元损失和阿尔茨海默病的缺失。在整个大脑中发现了体积损失的特征模式,这取决于发病的年龄和临床症状。在所有帕金森病患者中,内侧颞叶结构的损失都相当。这种萎缩在程度上与阿尔茨海默氏症相似,很可能是这些患者组中发现的记忆缺陷的解剖学基础。额叶萎缩是迟发性帕金森病(轻度萎缩)和弥漫性路易体病(严重萎缩)组的一个特征,所有病例都有痴呆。额叶萎缩与这些患者的运动症状持续时间相关,可能提示多巴胺能神经传递障碍、额叶萎缩和痴呆之间存在关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regional brain atrophy in idiopathic parkinson's disease and diffuse Lewy body disease.

This study measured brain atrophy in patients with idiopathic Parkinson's disease and diffuse Lewy body disease, all of whom had equivalent loss of midbrain dopammergic neurons and absence of Alzheimer's disease. Characteristic patterns of volume loss were found throughout the brain, depending on the age of onset and clinical signs. An equivalent loss of medial temporal lobe structures occurred in all parkinsonian patients. This atrophy was similar in magnitude to that seen in Alzheimer's disease and is likely to be the anatomical substrate for the memory deficits found in each of these patients groups. Frontal lobe atrophy was a feature of both late-onset Parkinson's disease (mild atrophy) and diffuse Lewy body disease (significant atrophy) groups, with all cases analyzed having dementia. Atrophy of frontal lobes correlated with the duration of motor symptoms in these patients and may suggest an association between dopammergic deafferentation, frontal atrophy and dementia.

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