AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Neurologie, Institut de la mémoire et de la maladie d'Alzheimer, Groupe Hospitalier Pitié-Salpêtrière, Paris, France; ICM, CNRS UMR 7225, Inserm U 1127, UPMC-P6 UMR S 1127, GH Pitié-Salpêtrière, Paris, France.
AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Département de Neurologie, Institut de la mémoire et de la maladie d'Alzheimer, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Alzheimers Dement. 2017 Apr;13(4):454-467. doi: 10.1016/j.jalz.2016.12.003. Epub 2017 Feb 7.
Preclinical Alzheimer's disease (AD) is a relatively recent concept describing an entity characterized by the presence of a pathophysiological biomarker signature characteristic for AD in the absence of specific clinical symptoms. There is rising interest in the scientific community to define such an early target population mainly because of failures of all recent clinical trials despite evidence of biological effects on brain amyloidosis for some compounds. A conceptual framework has recently been proposed for this preclinical phase of AD. However, few data exist on this silent stage of AD. We performed a systematic review to investigate how the concept is defined across studies. The review highlights the substantial heterogeneity concerning the three main determinants of preclinical AD: "normal cognition," "cognitive decline," and "AD pathophysiological signature." We emphasize the need for a harmonized nomenclature of the preclinical AD concept and standardized population-based and case-control studies using unified operationalized criteria.
临床前阿尔茨海默病(AD)是一个相对较新的概念,用于描述一种病症,其特征是存在 AD 的病理生理学生物标志物特征,但没有特定的临床症状。科学界对定义这样一个早期目标人群越来越感兴趣,主要是因为尽管一些化合物对大脑淀粉样蛋白有生物学作用,但最近所有的临床试验都失败了。最近提出了一个 AD 临床前阶段的概念框架。然而,关于 AD 的这一沉默阶段的数据很少。我们进行了一项系统评价,以研究该概念在不同研究中的定义。该综述突出了临床前 AD 的三个主要决定因素(“正常认知”、“认知能力下降”和“AD 病理生理学特征”)方面存在的实质性异质性。我们强调需要对临床前 AD 概念采用协调一致的命名法,并使用统一的操作性标准开展基于人群的和病例对照研究。