Evidence map›Paper›PMID 41724810›Full record

ArticleNpj mental health research2026

A systematic exploration of digital biomarkers for the detection of depressive episodes in bipolar disorder.

Ramzi Halabi, Benoit H Mulsant, Mirkamal Tolend, Daniel M Blumberger, Alexandra DeShaw, Arend Hintze, Christina Gonzalez-Torres, Muhammad I Husain, Helena K Kim, Claire O'Donovan and 2 more

Abstract read
In one paragraph

Article in Npj mental health research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

12 authors.

Ramzi HalabiCampbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Benoit H MulsantCampbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Mirkamal TolendCampbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Daniel M Blumberger *Campbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Alexandra DeShaw *Department of Psychiatry, Dalhousie University, Halifax, NS, Canada.
Arend Hintze *Department of MicroData Analytics, Dalarna University, Falun, Sweden.
Christina Gonzalez-Torres *Parkwood Institute: Finch Family Health Building, St. Joseph's Healthcare London, London, ON, Canada.
Muhammad I Husain *Campbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Helena K Kim *Campbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Claire O'Donovan *Department of Psychiatry, Dalhousie University, Halifax, NS, Canada.
Martin AldaDepartment of Psychiatry, Dalhousie University, Halifax, NS, Canada.
Abigail OrtizCampbell Family Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada. tania.ortizdominguez@utsouthwestern.edu.

Funding

CIHR 02010PJT-450770-BSB-CEAH-188794Ministerstvo Zdravotnictví Ceské Republiky NU23-04-00534NIMH NIH HHS 1R21MH123849-01A1
6 · The paper itself

Abstract

Digital phenotyping promises to transform psychiatry by using multimodal, densely sampled data. However, its potential is hindered by the lack of focus on identifying and validating digital biomarkers that accurately reflect mental states before evaluating their impact on outcomes. This longitudinal study used explainable machine learning to analyze multivariate, densely sampled data from 133 bipolar disorder (BD) participants over a median of 251 days, identifying robust digital biomarkers defining depressive episodes. The analysis included features from email-based daily self-reported mood, energy, and anxiety, as well as passively collected activity and sleep data using an Oura ring. The most robust descriptors of depressive episodes were lower daily mood variability, lower daily activity variability, and higher daily sleep onset latency variability. Self-reported daily mood features achieved the highest performance (AU-ROC: 0.82 ± 0.03). Our results establish the value of multimodal data and represent a critical first step toward automated detection and prediction of illness episodes in BD.

Identifiers

PMID41724810
PMCPMC12926226

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.