From the Civin Laboratory for Neuropathology, Banner Sun Health Research Institute, Sun City, Arizona, USA.
J Neuropathol Exp Neurol. 2022 May 20;81(6):387-413. doi: 10.1093/jnen/nlac030.
Senile plaques have been studied in postmortem brains for more than 120 years and the resultant knowledge has not only helped us understand the etiology and pathogenesis of Alzheimer disease (AD), but has also pointed to possible modes of prevention and treatment. Within the last 15 years, it has become possible to image plaques in living subjects. This is arguably the single greatest advance in AD research since the identification of the Aβ peptide as the major plaque constituent. The limitations and potentialities of amyloid imaging are still not completely clear but are perhaps best glimpsed through the perspective gained from the accumulated postmortem histological studies. The basic morphological classification of plaques into neuritic, cored and diffuse has been supplemented by sophisticated immunohistochemical and biochemical analyses and increasingly detailed mapping of plaque brain distribution. Changes in plaque classification and staging have in turn contributed to changes in the definition and diagnostic criteria for AD. All of this information continues to be tested by clinicopathological correlations and it is through the insights thereby gained that we will best be able to employ the powerful tool of amyloid imaging.
老年斑在尸检大脑中已经被研究了 120 多年,由此产生的知识不仅帮助我们理解了阿尔茨海默病(AD)的病因和发病机制,而且还指出了可能的预防和治疗模式。在过去的 15 年里,已经有可能对活体受试者进行斑块成像。这可以说是自发现 Aβ肽作为主要斑块成分以来 AD 研究的最大进展。淀粉样蛋白成像的局限性和可能性尚不完全清楚,但通过对积累的尸检组织学研究获得的观点或许可以最好地了解。斑块的基本形态学分类为神经突、核心和弥漫性,现已通过复杂的免疫组织化学和生化分析以及越来越详细的斑块脑分布图谱得到补充。斑块分类和分期的变化反过来又导致了 AD 的定义和诊断标准的变化。所有这些信息都在继续通过临床病理相关性进行测试,正是通过由此获得的见解,我们才能最好地利用淀粉样蛋白成像这一强大工具。