Stricker Learning Span criterion validity: a remote self-administered multi-device compatible digital word list memory measure shows similar ability to differentiate amyloid and tau PET-defined biomarker groups as in-person Auditory Verbal Learning Test

被引:6
作者
Stricker, Nikki H. [1 ]
Stricker, John L. [2 ]
Frank, Ryan D. [3 ]
Fan, Winnie Z. [3 ]
Christianson, Teresa J. [3 ]
Patel, Jay S. [1 ]
Karstens, Aimee J. [1 ]
Kremers, Walter K. [3 ]
Machulda, Mary M. [1 ]
Fields, Julie A. [1 ]
Graff-Radford, Jonathan [4 ]
Jack Jr, Clifford R. R. [5 ]
Knopman, David S. [4 ]
Mielke, Michelle M. [6 ]
Petersen, Ronald C. [4 ]
机构
[1] Mayo Clin Rochester, Dept Psychiat & Psychol, Rochester, MN 55905 USA
[2] Mayo Clin Rochester, Dept Informat Technol, Rochester, MN USA
[3] Mayo Clin Rochester, Dept Quantitat Hlth Sci, Rochester, MN USA
[4] Mayo Clin Rochester, Dept Neurol, Rochester, MN USA
[5] Mayo Clin Rochester, Dept Radiol, Rochester, MN USA
[6] Wake Forest Univ, Dept Epidemiol & Prevent, Sch Med, Winston Salem, NC USA
基金
美国国家卫生研究院;
关键词
mobile health; Alzheimer's disease; neuropsychology; aging; cognition; telemedicine; smartphone; neuropsychological tests; MILD COGNITIVE IMPAIRMENT; COGSTATE BRIEF BATTERY; ALZHEIMERS-DISEASE; OLDER-ADULTS; DIAGNOSTIC-ACCURACY; DEMENTIA; DECLINE; PERFORMANCE; AGE;
D O I
10.1017/S1355617723000322
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective:The Stricker Learning Span (SLS) is a computer-adaptive digital word list memory test specifically designed for remote assessment and self-administration on a web-based multi-device platform (Mayo Test Drive). We aimed to establish criterion validity of the SLS by comparing its ability to differentiate biomarker-defined groups to the person-administered Rey's Auditory Verbal Learning Test (AVLT). Method:Participants (N = 353; mean age = 71, SD = 11; 93% cognitively unimpaired [CU]) completed the AVLT during an in-person visit, the SLS remotely (within 3 months) and had brain amyloid and tau PET scans available (within 3 years). Overlapping groups were formed for 1) those on the Alzheimer's disease (AD) continuum (amyloid PET positive, A+, n = 125) or not (A-, n = 228), and those with biological AD (amyloid and tau PET positive, A+T+, n = 55) vs no evidence of AD pathology (A-T-, n = 195). Analyses were repeated among CU participants only. Results:The SLS and AVLT showed similar ability to differentiate biomarker-defined groups when comparing AUROCs (p's > .05). In logistic regression models, SLS contributed significantly to predicting biomarker group beyond age, education, and sex, including when limited to CU participants. Medium (A- vs A+) to large (A-T- vs A+T+) unadjusted effect sizes were observed for both SLS and AVLT. Learning and delay variables were similar in terms of ability to separate biomarker groups. Conclusions:Remotely administered SLS performed similarly to in-person-administered AVLT in its ability to separate biomarker-defined groups, providing evidence of criterion validity. Results suggest the SLS may be sensitive to detecting subtle objective cognitive decline in preclinical AD.
引用
收藏
页码:138 / 151
页数:14
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