From INSERM UMR-S U1237 (E.M.A.-U.), Université de Caen-Normandie, Caen, Normandy, France; and Department of Radiology (P.V.), Mayo Clinic, Rochester, MN.
Neurology. 2018 Apr 10;90(15):695-703. doi: 10.1212/WNL.0000000000005303. Epub 2018 Mar 28.
Preventing or delaying Alzheimer disease (AD) through lifestyle interventions will come from a better understanding of the mechanistic underpinnings of (1) why a significant proportion of elderly remain cognitively normal with AD pathologies (ADP), i.e., amyloid or tau; and (2) why some elderly individuals do not have significant ADP. In the last decades, concepts such as brain reserve, cognitive reserve, and more recently brain maintenance have been proposed along with more general notions such as (neuro)protection and compensation. It is currently unclear how to effectively apply these concepts in the new field of preclinical AD specifically separating the 2 distinct mechanisms of coping with pathology vs avoiding pathology. We propose a simplistic conceptual framework that builds on existing concepts using the nomenclature of resistance in the context of avoiding pathology, i.e., remaining cognitively normal without significant ADP, and resilience in the context of coping with pathology, i.e., remaining cognitively normal despite significant ADP. In the context of preclinical AD studies, we (1) define these concepts and provide recommendations (and common scenarios) for their use; (2) discuss how to employ this terminology in the context of investigating mechanisms and factors; (3) highlight the complementarity and clarity they provide to existing concepts; and (4) discuss different study designs and methodologies. The application of the proposed framework for framing hypotheses, study design, and interpretation of results and mechanisms can provide a consistent framework and nomenclature for researchers to reach consensus on identifying factors that may prevent ADP or delay the onset of cognitive impairment.
通过生活方式干预来预防或延缓阿尔茨海默病(AD),需要更好地理解以下两个方面的机制基础:(1)为什么相当一部分老年人患有 AD 病理(ADP),如淀粉样蛋白或 tau 蛋白,但认知仍正常;(2)为什么有些老年人没有明显的 ADP。在过去几十年中,提出了脑储备、认知储备等概念,最近又提出了脑维持等概念,以及更普遍的神经保护和代偿等概念。目前尚不清楚如何将这些概念有效地应用于临床前 AD 这一新领域,特别是要区分应对病理和避免病理的两种不同机制。我们提出了一个简单的概念框架,该框架基于现有的概念,在避免病理的情况下使用抗性术语,即没有明显 ADP 的认知仍正常,在应对病理的情况下使用恢复力术语,即尽管存在明显的 ADP,但认知仍正常。在临床前 AD 研究中,我们(1)定义了这些概念,并提供了使用这些概念的建议(和常见情况);(2)讨论如何在研究机制和因素的背景下使用这种术语;(3)强调它们对现有概念的互补性和清晰性;(4)讨论不同的研究设计和方法。该框架可用于提出假设、设计研究以及解释结果和机制,为研究人员提供一个一致的框架和术语,以就可能预防 ADP 或延缓认知障碍发作的因素达成共识。