Rius-Pérez S, Tormos A M, Pérez S, Taléns-Visconti R
Departamento de Fisiología, Facultad de Farmacia, Universidad de Valencia, Burjassot, Valencia, España.
Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Valencia, Burjassot, Valencia, España.
Neurologia (Engl Ed). 2018 Mar;33(2):112-120. doi: 10.1016/j.nrl.2015.07.010. Epub 2015 Sep 16.
Alzheimer disease (AD) is the main cortical neurodegenerative disease. The incidence of this disease increases with age, causing significant medical, social and economic problems, especially in countries with ageing populations.
This review aims to highlight existing evidence of how vascular dysfunction may contribute to cognitive impairment in AD, as well as the therapeutic possibilities that might arise from this evidence.
The vascular hypothesis emerged as an alternative to the amyloid cascade hypothesis as an explanation for the pathophysiology of AD. This hypothesis locates blood vessels as the origin for a variety of pathogenic pathways that lead to neuronal damage and dementia. Destruction of the organisation of the blood brain barrier, decreased cerebral blood flow, and the establishment of an inflammatory context would thus be responsible for any subsequent neuronal damage since these factors promote aggregation of β-amyloid peptide in the brain. The link between neurodegeneration and vascular dysfunction pathways has provided new drug targets and therapeutic approaches that will add to the treatments for AD.
It is difficult to determine whether the vascular component in AD is the cause or the effect of the disease, but there is no doubt that vascular pathology has an important relationship with AD. Vascular dysfunction is likely to act synergistically with neurodegenerative changes in a cycle that exacerbates the cognitive impairment found in AD.
阿尔茨海默病(AD)是主要的皮质神经退行性疾病。该疾病的发病率随年龄增长而增加,会引发重大的医学、社会和经济问题,在人口老龄化国家尤为如此。
本综述旨在强调现有证据,证明血管功能障碍如何导致AD患者的认知障碍,以及基于该证据可能产生的治疗可能性。
血管假说作为淀粉样蛋白级联假说的替代理论出现,用于解释AD的病理生理学。该假说认为血管是导致神经元损伤和痴呆的多种致病途径的起源。血脑屏障组织结构的破坏、脑血流量的减少以及炎症环境的形成,会导致随后的神经元损伤,因为这些因素会促进β-淀粉样肽在大脑中的聚集。神经退行性变与血管功能障碍途径之间的联系提供了新的药物靶点和治疗方法,可用于AD的治疗。
很难确定AD中的血管成分是该疾病的病因还是结果,但毫无疑问,血管病变与AD有重要关系。血管功能障碍可能与神经退行性变协同作用,形成一个循环,加剧AD患者的认知障碍。