Evidence map›Paper›PMID 37903878›Full record

ArticleScientific reports2023

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

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 and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Biomarker Methodologies: A NIMH Perspective.Advances in neurobiology · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 8 institutions in 2 countries.

Srinivasan VairavanJanssen Research & Development, LLC, 1125 Trenton Harbourton Road, Titusville, NJ, 08560, USA. svairava@its.jnj.com.
Homa RashidisabetDepartment of Bioengineering, University of Illinois Chicago, Chicago, IL, USA.
Qingqin S LiJanssen Research & Development, LLC, 1125 Trenton Harbourton Road, Titusville, NJ, 08560, USA.
Seth NessJanssen Research & Development, LLC, 1125 Trenton Harbourton Road, Titusville, NJ, 08560, USA.
Randall L MorrisonJanssen Research & Development, LLC, 1125 Trenton Harbourton Road, Titusville, NJ, 08560, USA.
Claudio N SoaresDepartment of Psychiatry, Queen's University School of Medicine, Kingston, ON, Canada.
Rudolf UherDepartment of Psychiatry, Dalhousie University, Halifax, Canada.
Benicio N FreyDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.
Raymond W LamDepartment of Psychiatry, University of British Columbia, Vancouver, Canada.
Sidney H KennedyCentre for Depression and Suicide Studies, Unity Health Toronto, Toronto, Canada.
Madhukar TrivediPeter O'Donnell Jr. Brain Institute and the Department of Psychiatry, UT Southwestern Medical Center, Dallas, TX, USA.
Wayne C DrevetsJanssen Research & Development, LLC, 1125 Trenton Harbourton Road, Titusville, NJ, 08560, USA.
Vaibhav A NarayanJanssen Research & Development, LLC, 1125 Trenton Harbourton Road, Titusville, NJ, 08560, USA.
Janssen (United States) · USDalhousie University · CAMcMaster University · CAQueen's University · CAThe University of Texas Southwestern Medical Center · USUnity Health TorontoUniversity of British Columbia · CAUniversity of Illinois Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Major Depressive DisorderBiomarkersChronic DiseaseHumansRecurrenceSelf ReportBiomarkers

Identifiers

PMID37903878
PMCPMC10616277
OpenAlexW4388023568

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.