Personalized relapse prediction in patients with major depressive disorder using digital biomarkers

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作者
Srinivasan Vairavan
Homa Rashidisabet
Qingqin S. Li
Seth Ness
Randall L. Morrison
Claudio N. Soares
Rudolf Uher
Benicio N. Frey
Raymond W. Lam
Sidney H. Kennedy
Madhukar Trivedi
Wayne C. Drevets
Vaibhav A. Narayan
机构
[1] Janssen Research & Development,Department of Bioengineering
[2] LLC,Department of Psychiatry
[3] University of Illinois Chicago,Department of Psychiatry
[4] Queen’s University School of Medicine,Department of Psychiatry and Behavioural Neurosciences
[5] Dalhousie University,Mood Disorders Program
[6] McMaster University,Department of Psychiatry
[7] St. Joseph’s Healthcare Hamilton,Centre for Depression and Suicide Studies
[8] University of British Columbia,Krembil Neurosciences
[9] Unity Health Toronto,Department of Psychiatry
[10] University Health Network,Peter O’Donnell Jr. Brain Institute and the Department of Psychiatry
[11] University of Toronto,undefined
[12] UT Southwestern Medical Center,undefined
[13] Davos Alzheimer’s Collaborative,undefined
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摘要
Major depressive disorder (MDD) is a chronic illness wherein relapses contribute to significant patient morbidity and mortality. Near-term prediction of relapses in MDD patients has the potential to improve outcomes by helping implement a ‘predict and preempt’ paradigm in clinical care. In this study, we developed a novel personalized (N-of-1) encoder-decoder anomaly detection-based framework of combining anomalies in multivariate actigraphy features (passive) as triggers to utilize an active concurrent self-reported symptomatology questionnaire (core symptoms of depression and anxiety) to predict near-term relapse in MDD. The framework was evaluated on two independent longitudinal observational trials, characterized by regular bimonthly (every other month) in-person clinical assessments, weekly self-reported symptom assessments, and continuous activity monitoring data with two different wearable sensors for ≥ 1 year or until the first relapse episode. This combined passive-active relapse prediction framework achieved a balanced accuracy of ≥ 71%, false alarm rate of ≤ 2.3 alarm/patient/year with a median relapse detection time of 2–3 weeks in advance of clinical onset in both studies. The study results suggest that the proposed personalized N-of-1 prediction framework is generalizable and can help predict a majority of MDD relapses in an actionable time frame with relatively low patient and provider burden.
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