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Preclinical Alzheimer's disease criteria

机译:临床前阿尔茨海默氏病标准

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摘要

We agree with Prof Petersen in his Comment1 that the findings in our Article, which used CSF measures, and those of the Mayo Clinic Study of Aging (MCSA),3 which used imaging variables, together provide strong support for the construct of preclinical Alzheimer's disease (AD). As illustrated in Prof Petersen's figure, the frequencies of the stages as defined in the two studies are virtually identical. However, several inaccuracies in the Comment warrant correction to prevent misinterpretation of our data. Prof Petersen writes that we "state that participants are either normal (clinical dementia rating [CDR] 0), or have dementia (CDR >0.5); there is no predementia symptomatic state". This is untrue. We state "the global CDR stages are 0, indicating cognitive normality, and 0.5, 1, 2 and 3, indicating very mild impairment or very mild dementia, and mild, moderate, and severe dementia, respectively" (second paragraph, second page). We further state that "in individuals with a CDR score of 0.5, AD was diagnosed if a score of at least O.5 was given for memory and at least one other domain and the clinician deemed the cognitive impairments to be due to AD (probable AD; referred to as CDR 0.5, symptomatic AD)."
机译:我们同意Petersen教授的评论1,我们的文章中的研究结果使用了CSF手段,而Mayo衰老临床研究(MCSA)3则使用了成像变量,共同为临床前阿尔茨海默氏病的构建提供了有力支持(广告)。正如彼得森教授的图所示,两项研究中定义的阶段频率实际上是相同的。但是,注释中的一些不正确之处需要更正,以防止对我们的数据进行误解。彼得森教授写道,“我们声明参与者要么正常(临床痴呆评分[CDR] 0],要么患有痴呆(CDR> 0.5);没有痴呆前症状状态”。这是不正确的。我们指出“全球CDR阶段分别为0,表明认知正常,而0.5、1、2和3,分别表明非常轻度的损伤或非常轻度的痴呆,以及轻度,中度和重度痴呆”(第二段,第二页) 。我们进一步指出,“在CDR得分为0.5的个体中,如果记忆力得分至少为O.5,且至少有一个其他领域得分,则诊断为AD,并且临床医生认为认知障碍是由AD引起的(可能AD;简称为CDR 0.5,即症状性AD)。”

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