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一位皮克病患者的认知、神经影像学和病理学研究。

Cognitive, neuroimaging, and pathological studies in a patient with Pick's disease.

作者信息

Lieberman A P, Trojanowski J Q, Lee V M, Balin B J, Ding X S, Greenberg J, Morrison D, Reivich M, Grossman M

机构信息

Department of Pathology, University of Pennsylvania Medical Center, USA.

出版信息

Ann Neurol. 1998 Feb;43(2):259-65. doi: 10.1002/ana.410430218.

Abstract

We conducted cognitive, imaging, and neuropathological studies on a patient with Pick's disease. The patient was impaired at interpreting sentences with complex grammatical constructions, differing significantly from control subjects and patients with Alzheimer's disease (AD). Evaluation of regional brain functioning at rest, with positron emission tomography, revealed reduced left frontal activity compared with control subjects and AD patients. Autopsy demonstrated the classic pathology of Pick's disease, including massive neuron loss and gliosis in the frontal and cingulate cortex as well as numerous tau-positive hippocampal Pick bodies. The abnormal tau proteins were phosphorylated at the same amino acid residues as AD paired helical filament tau (PHFtau), but they exhibited a unique migration profile on western blot. Our observations support the hypothesis that a distinct variety of hyperphosphorylated tau in Pick's disease compromises the long-term viability of selectively vulnerable populations of neurons in frontal cortices that contribute to sentence processing.

摘要

我们对一名患有皮克病的患者进行了认知、影像学和神经病理学研究。该患者在理解具有复杂语法结构的句子方面存在障碍,与对照组以及阿尔茨海默病(AD)患者有显著差异。通过正电子发射断层扫描对静息状态下的区域脑功能进行评估,结果显示与对照组和AD患者相比,该患者左侧额叶活动减少。尸检显示出皮克病的典型病理特征,包括额叶和扣带回皮质大量神经元丢失和胶质细胞增生,以及众多tau阳性的海马皮克小体。异常的tau蛋白在与AD双螺旋丝tau(PHFtau)相同的氨基酸残基处发生磷酸化,但在蛋白质印迹上呈现出独特的迁移图谱。我们的观察结果支持这样一种假说,即皮克病中一种独特的高度磷酸化tau变体损害了额叶皮质中对句子处理有贡献的选择性易损神经元群体的长期生存能力。

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