Raz Limor, Knoefel Janice, Bhaskar Kiran
J Cereb Blood Flow Metab. 2016 Jan;36(1):172-86. doi: 10.1038/jcbfm.2015.164.
The prevalence of dementia is increasing in our aging population at an alarming rate. Because of the heterogeneity of clinical presentation and complexity of disease neuropathology, dementia classifications remain controversial. Recently, the National Plan to address Alzheimer’s Disease prioritized Alzheimer’s disease-related dementias to include: Alzheimer’s disease, dementia with Lewy bodies, frontotemporal dementia, vascular dementia, and mixed dementias. While each of these dementing conditions has their unique pathologic signature, one common etiology shared among all these conditions is cerebrovascular dysfunction at some point during the disease process. The goal of this comprehensive review is to summarize the current findings in the field and address the important contributions of cerebrovascular, physiologic, and cellular alterations to cognitive impairment in these human dementias. Specifically, evidence will be presented in support of small-vessel disease as an underlying neuropathologic hallmark of various dementias, while controversial findings will also be highlighted. Finally, the molecular mechanisms shared among all dementia types including hypoxia, oxidative stress, mitochondrial bioenergetics, neuroinflammation, neurodegeneration, and blood–brain barrier permeability responsible for disease etiology and progression will be discussed.
在我们老龄化的人口中,痴呆症的患病率正以惊人的速度上升。由于临床表现的异质性和疾病神经病理学的复杂性,痴呆症的分类仍然存在争议。最近,应对阿尔茨海默病的国家计划将与阿尔茨海默病相关的痴呆症列为优先事项,包括:阿尔茨海默病、路易体痴呆、额颞叶痴呆、血管性痴呆和混合性痴呆。虽然这些痴呆病症中的每一种都有其独特的病理特征,但所有这些病症共有的一个常见病因是在疾病过程中的某个阶段出现脑血管功能障碍。这篇综述的目的是总结该领域的当前研究结果,并探讨脑血管、生理和细胞改变对这些人类痴呆症认知障碍的重要影响。具体而言,将提供证据支持小血管疾病是各种痴呆症潜在的神经病理学标志,同时也将突出有争议的研究结果。最后,将讨论所有痴呆症类型共有的分子机制,包括缺氧、氧化应激、线粒体生物能量学、神经炎症、神经退行性变以及负责疾病病因和进展的血脑屏障通透性。