Digital biomarker‐based individualized prognosis for people at risk of dementia

Background Research investigating treatments and interventions for cognitive decline fail due to difficulties in accurately recognizing behavioral signatures in the presymptomatic stages of the disease. For this validation study, we took our previously constructed digital biomarker‐based prognostic...

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Published inAlzheimer's & dementia : diagnosis, assessment & disease monitoring Vol. 12; no. 1; pp. e12073 - n/a
Main Authors Buegler, Maximilian, Harms, Robbert L., Balasa, Mircea, Meier, Irene B., Exarchos, Themis, Rai, Laura, Boyle, Rory, Tort, Adria, Kozori, Maha, Lazarou, Eutuxia, Rampini, Michaela, Cavaliere, Carlo, Vlamos, Panagiotis, Tsolaki, Magda, Babiloni, Claudio, Soricelli, Andrea, Frisoni, Giovanni, Sanchez‐Valle, Raquel, Whelan, Robert, Merlo‐Pich, Emilio, Tarnanas, Ioannis
Format Journal Article
LanguageEnglish
Published Hoboken John Wiley & Sons, Inc 2020
John Wiley and Sons Inc
Wiley
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Online AccessGet full text
ISSN2352-8729
2352-8729
DOI10.1002/dad2.12073

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Summary:Background Research investigating treatments and interventions for cognitive decline fail due to difficulties in accurately recognizing behavioral signatures in the presymptomatic stages of the disease. For this validation study, we took our previously constructed digital biomarker‐based prognostic models and focused on generalizability and robustness of the models. Method We validated prognostic models characterizing subjects using digital biomarkers in a longitudinal, multi‐site, 40‐month prospective study collecting data in memory clinics, general practitioner offices, and home environments. Results Our models were able to accurately discriminate between healthy subjects and individuals at risk to progress to dementia within 3 years. The model was also able to differentiate between people with or without amyloid neuropathology and classify fast and slow cognitive decliners with a very good diagnostic performance. Conclusion Digital biomarker prognostic models can be a useful tool to assist large‐scale population screening for the early detection of cognitive impairment and patient monitoring over time.
Bibliography:The work includes human subjects and follows the Declaration of Helsinki guidelines. Informed consent was obtained for experimentation. The privacy rights of human subjects were always observed.
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ISSN:2352-8729
2352-8729
DOI:10.1002/dad2.12073