Center for Alzheimer's Research, Banner Sun Health Research Institute, Sun City, AZ, USA.
J Alzheimers Dis. 2011;24(4):657-68. doi: 10.3233/JAD-2011-101884.
Two centuries ago, the German bacteriologist Robert Koch proposed three postulates to support a causal relationship between a specific microbe and an infectious disease. Similarly, three postulates are formulated here to help evaluate hypothetical proposals attempting to explain the pathogenesis of Alzheimer's disease (AD). The first postulate requires that the cause of AD precedes the cognitive decline and neurodegenerative pathology that characterize AD. This rule identifies a primary event from a neuropathological effect generated by the disease process. The second postulate stipulates that interventions aimed at the proposed causal event should prevent or reverse the cognitive and neurodegenerative pathology associated with AD prior to disease onset. This postulate emphasizes prevention or reversal of emerging neurocognitive pathology considerably before AD onset. If the first and second postulate requirements are met, the third postulate follows that interventions targeting the causal event should significantly lower the incidence of AD. For a causal hypothesis to be considered "likely" pathogenic to AD, support from all three postulates is a requisite. The pragmatic potential of the three postulates was applied to seven proposals using evidence-based meta-analysis mainly from randomized controlled trials. Proposals included the amyloid-β, cell cycle, cholinergic, inflammatory, oxidative stress, tau, and vascular hypotheses. Clinical evidence derived from each proposal formed the basis for an inferential conclusion based on the level of confidence provided by the trial data. The three postulates may challenge or help validate a proposed cause-effect relationship to AD and serve as a useful model for designing more intelligent therapeutic interventions aimed at preventing AD.
两百年前,德国细菌学家罗伯特·科赫(Robert Koch)提出了三个假定,以支持特定微生物与传染病之间的因果关系。同样,这里也提出了三个假定,以帮助评估试图解释阿尔茨海默病(AD)发病机制的假设性建议。
第一个假定要求 AD 的病因先于 AD 所特有的认知能力下降和神经退行性病理。这条规则从疾病过程产生的神经病理学效应中确定了一个主要事件。
第二个假定规定,针对所提议的因果事件的干预措施应在疾病发作之前预防或逆转与 AD 相关的认知和神经退行性病理。这条假定强调了在 AD 发病之前,对新出现的神经认知病理进行预防或逆转。如果满足了前两个假定要求,则第三个假定就会随之而来,即针对因果事件的干预措施应显著降低 AD 的发病率。
对于一个因果假设被认为对 AD 具有“可能”的致病作用,那么这三个假定的支持是必要的。这三个假定的实用潜力已应用于七个建议,主要使用了基于随机对照试验的循证荟萃分析。建议包括淀粉样蛋白-β、细胞周期、胆碱能、炎症、氧化应激、tau 和血管假说。每个建议的临床证据构成了基于试验数据提供的置信水平的推断结论的基础。
这三个假定可能会挑战或有助于验证 AD 的因果关系,并为设计更智能的治疗干预措施以预防 AD 提供有用的模型。