Department of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, Texas.
Department of Neuroscience, Developmental and Regenerative Biology, The University of Texas at San Antonio, San Antonio, Texas.
Am J Pathol. 2022 Oct;192(10):1340-1346. doi: 10.1016/j.ajpath.2022.07.002. Epub 2022 Aug 2.
Alzheimer disease (AD) is a chronic disease characterized by a progressive decline in memory and cognition. AD progression is closely correlated with neuropathologic changes and accumulation of the two main hallmark lesions, senile plaques and neurofibrillary tangles. Nevertheless, deciphering the complex biological aspects of AD requires looking for the neuropathologic changes not only as the cause but also as the collective response to a disease process that is essential to maintaining life during aging but ultimately generates a nonfunctional brain. Chronic conditions, such as AD, represent a new homeostatic balance or disease state, where the organism responds or adapts to maintain life. The pathologic diagnosis of AD still remains the gold standard for precise diagnosis of dementia, commonly in conjunction with cognitive-memory tests and brain image scans. Herein, we present a general overview of the main neuropathologic hallmarks and features of AD and related dementia, revealing the key biological and functional changes as potential drivers of age-dependent brain failure related to AD. The present work reflects some of the main ideas presented during the American Society for Investigative Pathology Rous-Whipple Award Lecture 2021.
阿尔茨海默病(AD)是一种慢性疾病,其特征是记忆和认知能力的进行性下降。AD 的进展与神经病理变化密切相关,并且与两种主要标志性病变——老年斑和神经纤维缠结的积累有关。然而,要揭示 AD 的复杂生物学方面,不仅需要寻找神经病理变化作为病因,还需要寻找其作为对疾病过程的集体反应的原因,因为该疾病过程对于维持衰老过程中的生命至关重要,但最终会导致大脑失去功能。像 AD 这样的慢性疾病代表了一种新的体内平衡或疾病状态,在这种状态下,机体通过响应或适应来维持生命。AD 的病理诊断仍然是痴呆症的金标准,通常与认知记忆测试和大脑图像扫描相结合。在此,我们对 AD 和相关痴呆症的主要神经病理标志和特征进行了概述,揭示了潜在的生物和功能变化作为与 AD 相关的年龄依赖性大脑衰竭的潜在驱动因素。本工作反映了 2021 年美国调查病理学 Rous-Whipple 奖演讲中提出的一些主要观点。