Sperling Reisa, Johnson Keith
Brigham and Women’s Hospital, Memory Disorders Unit, 221 Longwood Ave, Boston, MA 02115, USA.
Continuum (Minneap Minn). 2013 Apr;19(2 Dementia):325-38. doi: 10.1212/01.CON.0000429181.60095.99.
This article reviews recent advances in imaging and fluid biomarkers for Alzheimer disease (AD) and their application to newly proposed diagnostic criteria across the continuum of AD.
There have been remarkable developments in neuroimaging markers for AD over the past decade, most notably the advent of positron emission tomography (PET) amyloid imaging using radiotracers that label fibrillar forms of amyloid-β (Aβ). Similarly, new research in CSF markers suggests CSF levels of Aβ1-42 and phosphorylated tau may be useful in the early diagnosis of AD and prediction of cognitive decline. The National Institute on Aging and the Alzheimer's Association recently convened three workgroups to develop joint recommendations for new diagnostic guidelines across the spectrum of AD. These recommendations incorporate biomarkers and propose updated criteria for the previously recognized stage of AD dementia, the evolving definition of mild cognitive impairment, and a newly proposed concept of stages of preclinical AD.
Recent advances in AD biomarkers have increased the ability to detect evidence of early AD pathology in vivo. These biomarkers have been incorporated into new diagnostic recommendations, but a number of challenges remain for the biomarkers to become widely applied in clinical practice.
本文综述了阿尔茨海默病(AD)成像和流体生物标志物的最新进展及其在AD连续病程新提出的诊断标准中的应用。
在过去十年中,AD的神经成像标志物有了显著进展,最显著的是使用标记淀粉样β蛋白(Aβ)纤维形式的放射性示踪剂的正电子发射断层扫描(PET)淀粉样成像的出现。同样,脑脊液标志物的新研究表明,脑脊液中Aβ1-42和磷酸化tau蛋白水平可能有助于AD的早期诊断和认知衰退的预测。美国国立衰老研究所和阿尔茨海默病协会最近召集了三个工作组,为AD全病程制定新诊断指南的联合建议。这些建议纳入了生物标志物,并对先前公认的AD痴呆阶段、轻度认知障碍不断演变的定义以及新提出的临床前AD阶段概念提出了更新标准。
AD生物标志物的最新进展提高了在体内检测早期AD病理证据的能力。这些生物标志物已被纳入新的诊断建议中,但要使这些生物标志物在临床实践中得到广泛应用仍面临一些挑战。