Examining the diagnostic value of the mnemonic discrimination task for classification of cognitive status and amyloid-beta burden.
Examining the diagnostic value of the mnemonic discrimination task for classification of cognitive status and amyloid-beta burden.
复制标题
检查认知状态和淀粉样蛋白β负担的助记符歧视任务的诊断价值。
DOI:
10.1016/j.neuropsychologia.2023.108727
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发表时间:
2023-12-15
期刊:
影响因子:
2.6
通讯作者:
Yassa, Michael A.
中科院分区:
文献类型:
--
作者:
Kim, Soyun;Adams, Jenna N.;Chappel-Farley, Miranda G.;Keator, David;Janecek, John;Taylor, Lisa;Mikhail, Abanoub;Hollearn, Martina;Mcmillan, Liv;Rapp, Paul;Yassa, Michael A.
关键词:
Alzheimer’s disease (AD) is the most common type of dementia, characterized by early memory impairments and gradual worsening of daily functions. AD-related pathology, such as amyloid-beta (Aβ) plaques, begins to accumulate many years before the onset of clinical symptoms. Predicting risk for AD via related pathology is critical as the preclinical stage could serve as a therapeutic time window, allowing for early management of the disease and reducing health and economic costs. Current methods for detecting AD pathology, however, are often expensive and invasive, limiting wide and easy access to a clinical setting. A non-invasive, cost-efficient platform, such as computerized cognitive tests, could be potentially useful to identify at-risk individuals as early as possible. In this study, we examined the diagnostic value of an episodic memory task, the mnemonic discrimination task (MDT), for predicting risk of cognitive impairment or Aβ burden. We constructed a random forest classification algorithm, utilizing MDT performance metrics and various neuropsychological test scores as input features, and assessed model performance using area under the curve (AUC). Models based on MDT performance metrics achieved classification results with an AUC of 0.83 for cognitive status and an AUC of 0.64 for Aβ status. Our findings suggest that mnemonic discrimination function may be a useful predictor of progression to prodromal AD or increased risk of Aβ load, which could be a cost-efficient, noninvasive cognitive testing solution for potentially wide-scale assessment of AD pathological and cognitive risk.
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影响因子:
2.6
作者:
Aggleton, JP;Shaw, C
通讯作者:
Shaw, C
影响因子:
4.2
作者:
Ewers M;Walsh C;Trojanowski JQ;Shaw LM;Petersen RC;Jack CR Jr;Feldman HH;Bokde AL;Alexander GE;Scheltens P;Vellas B;Dubois B;Weiner M;Hampel H;North American Alzheimer's Disease Neuroimaging Initiative (ADNI)
通讯作者:
North American Alzheimer's Disease Neuroimaging Initiative (ADNI)
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Dietterich, TG
通讯作者:
Dietterich, TG
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3.7
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Arnold, Steven E.;Hyman, Bradley T.;Van Hoesen, Gary W.
通讯作者:
Van Hoesen, Gary W.
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3.6
作者:
Clark, D. G.;Kapur, P.;Geldmacher, D. S.;Brockington, J. C.;Harrell, L.;DeRamus, T. P.;Blanton, P. D.;Lokken, K.;Nicholas, A. P.;Marson, D. C.
通讯作者:
Marson, D. C.