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使用免疫组织化学对老年痴呆受试者脑病理学进行系统评估。

Systematic appraisal using immunohistochemistry of brain pathology in aged and demented subjects.

作者信息

Aho Leena, Parkkinen Laura, Pirttila Tuula, Alafuzoff Irina

机构信息

Department of Clinical Medicine, Unit of Neurology, Section of Neuropathology, Kuopio University, Kuopio, Finland.

出版信息

Dement Geriatr Cogn Disord. 2008;25(5):423-32. doi: 10.1159/000122963. Epub 2008 Apr 3.

Abstract

BACKGROUND/AIMS: Abnormal processing of hyperphosphorylated tau (HPtau), amyloid-beta (Abeta) and alpha-synuclein (alphaS) proteins is considered as causative with regard to the clinical symptoms in age-related neurodegenerative diseases.

METHODS

In this retrospective, postmortem study applying immunohistochemical methodology, we assessed Alzheimer's-disease (AD)-related HPtau and Abeta pathology in 178 subjects with alphaS pathology.

RESULTS

These pathologies were frequently seen concomitantly, i.e. HPtau in 83% and Abeta in 62% of the alphaS-positive cases. Furthermore, the striatum was frequently involved, particularly in subjects with cognitive impairment (65%). The predictive value of widespread HPtau pathology, i.e. stages V-VI, with respect to cognitive impairment was high, since all 18 subjects presenting with this stage were demented. In contrast, the predictive value of widespread alphaS pathology, i.e. stages 5-6 according to Braak's Parkinson disease staging, was debatable. Fifty-three percent of the subjects with widespread alphaS pathology and no or mild AD-related HPtau pathology were cognitively unimpaired. It is noteworthy that striatal Abeta pathology was more often seen in demented subjects independently of HPtau and/or alphaS status.

CONCLUSION

The causative pathology in subjects with clinically diagnosed dementia with Lewy bodies needs to be clarified in future studies.

摘要

背景/目的:在年龄相关性神经退行性疾病中,高磷酸化tau蛋白(HPtau)、淀粉样β蛋白(Abeta)和α-突触核蛋白(alphaS)的异常加工被认为与临床症状的产生有关。

方法

在这项采用免疫组化方法的回顾性尸检研究中,我们评估了178例存在alphaS病理改变的受试者的阿尔茨海默病(AD)相关HPtau和Abeta病理情况。

结果

这些病理改变经常同时出现,即在alphaS阳性病例中,83%存在HPtau,62%存在Abeta。此外,纹状体经常受累,尤其是在有认知障碍的受试者中(65%)。广泛的HPtau病理改变(即V-VI期)对认知障碍的预测价值较高,因为所有呈现此阶段的18名受试者均患有痴呆。相比之下,广泛的alphaS病理改变(即根据Braak帕金森病分期为5-6期)的预测价值存在争议。53%存在广泛alphaS病理改变且无或仅有轻度AD相关HPtau病理改变的受试者认知未受损。值得注意的是,无论HPtau和/或alphaS状态如何,痴呆受试者中更常出现纹状体Abeta病理改变。

结论

临床诊断为路易体痴呆的受试者的病因性病理改变有待未来研究进一步阐明。

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