Curiel Cid Rosie E, Crocco Elizabeth A, Duara Ranjan, Garcia Jessica M, Rosselli Monica, DeKosky Steven T, Smith Glenn, Bauer Russell, Chirinos Cesar L, Adjouadi Malek, Barker Warren, Loewenstein David A
Center for Cognitive Neuroscience and Aging, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, 1695 NW 9th Avenue, Miami, FL, 33136, USA.
Center for Cognitive Neuroscience and Aging, Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, 1695 NW 9th Avenue, Miami, FL, 33136, USA.
J Psychiatr Res. 2020 May;124:131-136. doi: 10.1016/j.jpsychires.2020.02.008. Epub 2020 Feb 10.
The development and validation of clinical outcome measures to detect early cognitive decline associated with Alzheimer's disease (AD) biomarkers is imperative. Semantic intrusions on the Loewenstein Acevedo Scales of Semantic Interference and Learning (LASSI-L) has outperformed widely used cognitive measures as an early correlate of elevated brain amyloid in prodromal AD and has distinguished those with amnestic mild cognitive impairment (aMCI) and high amyloid load from aMCI attributable to other non-AD conditions.
Since intrusion errors on memory tasks vary widely, we employed a novel method that accounts for the percentage of intrusion errors (PIE) in relation to total responses. Individuals with either high or low amyloid load across the spectrum of aMCI and dementia and amyloid negative cognitively normal older adults (CN) were studied.
Mean PIE on indices sensitive to proactive semantic interference (PSI) and failure to recover from proactive semantic interference (frPSI) could distinguish amyloid positive from amyloid negative aMCI and dementia groups. Number of correct responses alone, while able to differentiate the different diagnostic groups, did not differentiate amyloid positive aMCI from their counterparts without amyloid pathology.
PIE, a novel and sensitive index of early memory dysfunction, demonstrated high levels of sensitivity and specificity in differentiating CN from amyloid positive persons with preclinical AD. Mean levels of PIE are higher for amyloid positive aMCI and dementia participants relative to their amyloid negative counterparts.
开发和验证用于检测与阿尔茨海默病(AD)生物标志物相关的早期认知衰退的临床结局指标势在必行。在洛温斯坦·阿塞韦多语义干扰与学习量表(LASSI-L)上的语义侵入,作为前驱AD中脑淀粉样蛋白升高的早期相关指标,其表现优于广泛使用的认知测量指标,并且能够区分遗忘型轻度认知障碍(aMCI)且淀粉样蛋白负荷高的患者与由其他非AD疾病导致的aMCI患者。
由于记忆任务中的侵入错误差异很大,我们采用了一种新方法,该方法考虑了侵入错误百分比(PIE)与总反应的关系。我们研究了aMCI和痴呆症全谱中淀粉样蛋白负荷高或低的个体以及淀粉样蛋白阴性的认知正常老年人(CN)。
对主动语义干扰(PSI)和无法从主动语义干扰中恢复(frPSI)敏感的指标上的平均PIE能够区分淀粉样蛋白阳性和阴性的aMCI及痴呆症组。仅正确反应的数量虽然能够区分不同的诊断组,但无法区分淀粉样蛋白阳性的aMCI患者与其无淀粉样蛋白病理的对应患者。
PIE是一种早期记忆功能障碍的新颖且敏感的指标,在区分CN与临床前AD淀粉样蛋白阳性患者方面表现出高敏感性和特异性。淀粉样蛋白阳性的aMCI和痴呆症参与者的平均PIE水平相对于淀粉样蛋白阴性的对应者更高。