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阿尔茨海默病诊断标准:实用应用。

Alzheimer's disease diagnostic criteria: practical applications.

机构信息

Cleveland Clinic Lou Ruvo Center for Brain Health, 888 W. Bonneville Avenue, Las Vegas, NV 89106, USA.

出版信息

Alzheimers Res Ther. 2012 Sep 5;4(5):35. doi: 10.1186/alzrt138. eCollection 2012.

DOI:10.1186/alzrt138
PMID:22947665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3580392/
Abstract

Alzheimer's disease (AD) can be identified prior to the occurrence of dementia by using biomarkers. Three phases of AD are recognized: an asymptomatic biomarker-positive phase, a phase with positive biomarkers and mild cognitive deficits, and a dementia phase. Codification of these phases was first accomplished in 2007 by an International Work Group (IWG) led by Bruno Dubois. The definitions relevant to the approach were further clarified in 2010. In 2011, the National Institute on Aging/Alzheimer's Association (NIA/AA) established three work groups to develop definitions and criteria for these three phases of AD. The criteria of the IWG and those of the NIA/AA have many similarities and important differences. The two sets of criteria concur in recognizing the onset of AD prior to dementia. The three phases of AD described in both sets of criteria embrace the same clinical entities but with different terminologies and emphases. IWG criteria emphasize a single clinico-biological approach that includes all symptomatic phases of AD and uses the same diagnostic framework across the spectrum of symptomatic disease; the NIA/AA criteria apply different diagnostic approaches to the three phases. Biomarkers are an integrated and required part of the IWG criteria and are optional in the NIA/AA approach. Both sets of criteria have substantial strengths, but new information demonstrates shortcomings that can be addressed in future revisions of the criteria. These new criteria have profound implications, including greatly increasing the number of people identified as suffering from AD and increasing the time that patients will spend with knowledge of the presence of the disease.

摘要

阿尔茨海默病(AD)可以通过生物标志物在痴呆发生之前被识别。AD 分为三个阶段:无症状的生物标志物阳性阶段、有阳性生物标志物和轻度认知障碍的阶段以及痴呆阶段。这些阶段的编码于 2007 年由国际工作组(IWG)首次完成,该工作组由 Bruno Dubois 领导。2010 年进一步澄清了与该方法相关的定义。2011 年,美国国家老龄化研究所/阿尔茨海默病协会(NIA/AA)成立了三个工作组,制定 AD 这三个阶段的定义和标准。IWG 标准和 NIA/AA 标准有许多相似之处和重要区别。这两套标准都同意在痴呆症之前识别 AD 的发病。两套标准中描述的 AD 的三个阶段包含相同的临床实体,但术语和重点不同。IWG 标准强调单一的临床生物学方法,包括 AD 的所有有症状阶段,并在症状性疾病谱中使用相同的诊断框架;NIA/AA 标准对三个阶段采用不同的诊断方法。生物标志物是 IWG 标准的一个综合和必需部分,而在 NIA/AA 方法中是可选的。这两套标准都有很大的优势,但新信息表明标准存在可以在未来修订中解决的缺点。这些新标准具有深远的影响,包括大大增加了被认定患有 AD 的人数,并增加了患者了解疾病存在的时间。

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