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Smartphone-based detection of subtle memory decline in prodromal Alzheimer's disease.
Polk, S. E. (First author)DZNE* ; Clark, L. R. ; Basche, K. ; Kleineidam, L.DZNE* ; Glanz, W.DZNE* ; Butryn, M.DZNE* ; Perneczky, R.DZNE* ; Buerger, K.DZNE* ; Fliessbach, K.DZNE* ; Laske, C.DZNE* ; Spottke, A.DZNE* ; Schneider, A.DZNE* ; Wiltfang, J.DZNE* ; Teipel, S.DZNE* ; Bartels, C. ; Rostamzadeh, A. ; Janowitz, D.Extern* ; Rauchmann, B. S.Extern* ; Kilimann, I.DZNE* ; Sodenkamp, S.DZNE* ; Coenjaerts, M. ; Brosseron, F.DZNE* ; Wagner, M.DZNE* ; Frommann, I.DZNE* ; Stark, M.DZNE* ; Schmid, M.DZNE* ; Schott, B. H.DZNE* ; Johnson, S. C. ; Jessen, F.DZNE* ; Düzel, E.DZNE* ; Berron, D. (Last author)DZNE*
2026
Macmillan Publishers Limited
[Basingstoke]
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Please use a persistent id in citations: doi:10.1038/s41746-026-02731-1
Abstract: The slow progression of Alzheimer's disease (AD) poses a challenge for the quantification of early disease-driven cognitive decline. Here, we show that frequently administered remote and unsupervised digital cognitive assessments can detect differences in cognitive decline within 30 weeks in early AD. The sample comprised 202 individuals (52-85 years old) recruited from longitudinal observational studies, who were cognitively unimpaired (CU, n = 152) or had a diagnosis of mild cognitive impairment (MCI, n = 50). Participants self-administered remote tasks testing memory precision for objects and scenes, associative memory, and familiarity-dependent memory. The MCI group showed greater decline than the CU group in the familiarity-dependent task, while stratifying the MCI group by beta-amyloid (Aβ) status (n = 21 Aβ-; n = 24 Aβ+) revealed greater change in memory precision for objects and familiarity-dependent memory in the MCI Aβ+ group. A 30-week change in the remote familiarity-dependent task was correlated with a multi-year change in annual in-person neuropsychological assessments. In conclusion, frequent remote cognitive testing is a promising tool to feasibly capture and monitor subtle and short-term cognitive decline.
Contributing Institute(s):
- Clinical Cognitive Neuroscience (AG Berron)
- Neuropsychology (AG Wagner)
- Clinical Neurophysiology and Memory (AG Düzel)
- Vascular Cognitive Impairment & Post-Stroke Dementia (AG Dichgans)
- Clinical Research (Munich) (Clinical Research (Munich))
- Patient Studies (Bonn) (Patient Studies (Bonn))
- Parkinson Genetics (AG Gasser)
- Clinical Research Platform (CRP) (AG Spottke)
- Translational Dementia Research (Bonn) (AG Schneider)
- Molecular biomarkers for predictive diagnostics of neurodegenerative diseases (AG Wiltfang)
- Clinical Dementia Research (Rostock /Greifswald) (AG Teipel)
- Core ICRU (ICRU)
- Neuroinflammation, Biomarker (AG Heneka)
- Mathematics, statistics and informatics methods for support of population studies and clinical research (AG Schmid Bonn)
- Epigenetics and Systems Medicine in Neurodegenerative Diseases (AG Fischer)
- Clinical Alzheimer’s Disease Research (AG Jessen)
Research Program(s):
- 353 - Clinical and Health Care Research (POF4-353) (POF4-353)
- 352 - Disease Mechanisms (POF4-352) (POF4-352)
Database coverage:
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