Sakurai Hirofumi, Hanyu Haruo
Nihon Rinsho. 2016 Mar;74(3):438-41.
The pathophysiological process of Alzheimer's disease (AD) is thought to begin more than twenty years before the diagnosis of AD dementia. Recent studies provided the biomarker of AD pathological changes. Biomarkers of brain Aβ amyloidosis include reduction in cerebrospinal fluid (CSF) Aβ42 and increased amyloid tracer retention on positron emission tomography(PET) imaging. Elevated CSF tau is thought to be a biomarker of neuronal injury. The Natinal Institute on Aging and the Alzheimer's Association proposed AD dementia, mild cognitive impairment due to AD, the preclinical stage of AD. These recommendation for the biomarker of AD are intended for research purposes at this time. Some disease-modifying therapies may be effective for the preclinical stage of AD.
阿尔茨海默病(AD)的病理生理过程被认为在AD痴呆症诊断前二十多年就已开始。近期研究提供了AD病理变化的生物标志物。脑Aβ淀粉样变性的生物标志物包括脑脊液(CSF)中Aβ42减少以及正电子发射断层扫描(PET)成像中淀粉样示踪剂滞留增加。脑脊液中tau蛋白升高被认为是神经元损伤的生物标志物。美国国立衰老研究所和阿尔茨海默病协会提出了AD痴呆症、AD所致轻度认知障碍、AD临床前期的概念。目前,这些关于AD生物标志物的建议仅用于研究目的。一些疾病修饰疗法可能对AD临床前期有效。