Ersin Ersözlü, Lukas Preis, Aykut Aktuz, Louise Droste, Akin Erman, Daria Gref, Katharina Sophie Strentz, Julian Hellmann-Regen
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引用次数: 0
Abstract
Background: Accurate differentiation between mild and moderate dementia is increasingly important, particularly as amyloid-targeting therapies are restricted to early disease stages. Functional impairment in instrumental activities of daily living is a hallmark of progression beyond mild dementia. The informant-based Functional Activities Questionnaire (FAQ) is widely used, but empirically validated cut-offs distinguishing mild from moderate dementia remain insufficiently defined.
Methods: The optimal cut-off score was derived from the entire National Alzheimer's Coordinating Center (NACC) Uniform Data Set as a discovery cohort (n = 34,513) and validated in two independent multicentric cohorts (Alzheimer's Disease Neuroimaging Initiative (ADNI) n = 381 and Frontotemporal Lobar Degeneration Neuroimaging Initiative (FTLDNI) n = 74). The dementia staging was based on the Clinical Dementia Rating (CDR) global score. Functional impairment was assessed using the 10-item FAQ. Receiver operating characteristic analyses in NACC identified optimal thresholds, which were applied unchanged in validation cohorts. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated, and discordant cases were examined to identify factors associated with misclassification.
Results: In NACC, the FAQ demonstrated excellent discrimination of moderate dementia (AUC=0.947, 95% CI 0.944-0.949). A cut-off value of ≥18 maximized discrimination (sensitivity 96%, specificity 87%). A higher threshold of ≥23 improved specificity (92%), while maintaining sensitivity (83%). In ADNI and FTLDNI, the sensitivity of ≥18 threshold yielded 92% and 94%, respectively. Moreover, older age and lower cognitive performance were associated with higher odds of misclassification.
Conclusions: The FAQ robustly differentiates mild from moderate dementia across diverse cohorts. A threshold of ≥18 prioritizes sensitivity, whereas ≥23 favors specificity, supporting context-dependent functional staging in clinical and research settings. Individuals with FAQ scores between 18 and 22 may benefit from more detailed clinical staging.
背景:准确区分轻度和中度痴呆越来越重要,特别是淀粉样蛋白靶向治疗仅限于疾病早期阶段。日常生活工具活动的功能障碍是轻度痴呆症进展的标志。基于信息的功能活动问卷(FAQ)被广泛使用,但经验验证的区分轻度和中度痴呆的界限仍然不够明确。方法:最佳分值来自整个国家阿尔茨海默病协调中心(NACC)统一数据集,作为一个发现队列(n = 34,513),并在两个独立的多中心队列(阿尔茨海默病神经影像学倡议(ADNI) n = 381和额颞叶变性神经影像学倡议(FTLDNI) n = 74)中进行验证。痴呆分期是基于临床痴呆评分(CDR)全局评分。功能损害评估采用10项常见问题解答。NACC的受试者工作特征分析确定了最佳阈值,该阈值在验证队列中应用不变。计算敏感性、特异性、阳性预测值和阴性预测值,并检查不一致的病例,以确定与误分类相关的因素。结果:在NACC中,FAQ对中度痴呆具有很好的鉴别能力(AUC=0.947, 95% CI 0.944-0.949)。临界值≥18可获得最大的鉴别(灵敏度96%,特异性87%)。≥23的较高阈值可提高特异性(92%),同时保持敏感性(83%)。在ADNI和FTLDNI中,≥18阈值的敏感性分别为92%和94%。此外,年龄越大,认知能力越差,错误分类的几率越大。结论:FAQ在不同的队列中有力地区分了轻度和中度痴呆。≥18的阈值优先考虑敏感性,而≥23的阈值有利于特异性,支持临床和研究环境中与环境相关的功能分期。FAQ得分在18到22之间的个体可能会从更详细的临床分期中受益。
期刊介绍:
The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.