Department of Physiology, Faculty of Medicine, University of Valencia, Health Research Institute INCLIVA, Avda. Blasco Ibanez, 17, 46010 Valencia, Spain.
Department of Clinic Neurophysiology. University Clinic Hospital of Valencia, Avda. Blasco Ibanez, 19, 46010 Valencia, Spain.
Int J Mol Sci. 2019 Nov 6;20(22):5536. doi: 10.3390/ijms20225536.
While Alzheimer's disease (AD) classical diagnostic criteria rely on clinical data from a stablished symptomatic disease, newer criteria aim to identify the disease in its earlier stages. For that, they incorporated the use of AD's specific biomarkers to reach a diagnosis, including the identification of Aβ and tau depositions, glucose hypometabolism, and cerebral atrophy. These biomarkers created a new concept of the disease, in which AD's main pathological processes have already taken place decades before we can clinically diagnose the first symptoms. Therefore, AD is now considered a dynamic disease with a gradual progression, and dementia is its final stage. With that in mind, new models were proposed, considering the orderly increment of biomarkers and the disease as a continuum, or the variable time needed for the disease's progression. In 2011, the National Institute on Aging and the Alzheimer's Association (NIA-AA) created separate diagnostic recommendations for each stage of the disease continuum-preclinical, mild cognitive impairment, and dementia. However, new scientific advances have led them to create a unifying research framework in 2018 that, although not intended for clinical use as of yet, is a step toward shifting the focus from the clinical symptoms to the biological alterations and toward changing the future diagnostic and treatment possibilities. This review aims to discuss the role of biomarkers in the onset of AD.
虽然阿尔茨海默病(AD)的经典诊断标准依赖于已确诊的有症状疾病的临床数据,但新的标准旨在更早地识别出这种疾病。为此,它们采用了 AD 特定的生物标志物来进行诊断,包括识别 Aβ 和 tau 沉积物、葡萄糖代谢低下和脑萎缩。这些生物标志物创造了一个新的疾病概念,即 AD 的主要病理过程已经在我们能够临床诊断出最初症状的几十年前就发生了。因此,AD 现在被认为是一种具有逐渐进展的动态疾病,而痴呆是其最终阶段。考虑到这一点,人们提出了新的模型,认为生物标志物的有序增加和疾病作为一个连续体,或者疾病进展所需的时间是变量。2011 年,美国国家老龄化研究所和阿尔茨海默病协会(NIA-AA)为疾病连续体的每个阶段(临床前、轻度认知障碍和痴呆)分别制定了诊断建议。然而,新的科学进展促使他们在 2018 年创建了一个统一的研究框架,尽管目前尚未用于临床,但这是朝着从临床症状转向生物改变以及改变未来诊断和治疗可能性迈出的一步。本文旨在讨论生物标志物在 AD 发病中的作用。