Evidence map›Paper›PMID 40394283›Full record

ArticleMolecular psychiatry2025

Towards clinical subtypes in schizophrenia: integrating cognitive, functional, and digital phenotyping assessments.

Andrew Jin Soo Byun, Erlend Lane, Carsten Langholm, Matthew Flathers, Mei-Hua Hall, John B Torous

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2025. 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. Review
  2. 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

6 authors.

Andrew Jin Soo ByunJohn A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA. jinsoobyun@g.harvard.edu.ORCID http://orcid.org/0000-0003-2062-7647
Erlend LaneDivision of Digital Psychiatry, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Carsten LangholmDivision of Digital Psychiatry, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6178-2187
Matthew FlathersDivision of Digital Psychiatry, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0009-0004-3351-0688
Mei-Hua HallPsychosis Neurobiology Laboratory, McLean Hospital, Harvard Medical School, Belmont, MA, USA.ORCID http://orcid.org/0000-0002-4558-7023
John B TorousDivision of Digital Psychiatry, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-5362-7937

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterogeneity in the clinical presentation of schizophrenia impairs both proper and preventative care. The digital phenotyping data gathered from an international multi-site cohort study in people with schizophrenia (SZ) offers a novel opportunity to explore clinically meaningful subtypes in the context of clinical, functional, and cognitive data. Using a set of behavioral features derived from smartphone digital phenotyping, clinical assessment of symptoms including PANSS, clinical assessment of cognition with BACS, and clinical assessment of functioning with the social functioning assessments over the target period of twelve months, we found that the international cohort of 74 patients were categorized into three well-defined clusters that suggest clinically actionable targets from differential correlations in each. Namely, the identified clusters seemed to share phenotypic traits with the affective psychosis with more severe symptomatic presentation, a non-affective SZ with functional impairment, and a higher functioning non-affective SZ cluster. Partial correlation analysis further highlighted the emergence of different features per cluster, where anxiety symptoms were most notable for one group, whereas psychotic symptoms were most notable for the other two. Importantly, we showcase an analysis pipeline that transparently addresses challenges of missing data and potential skew so that this research methodology can be applied to future prospective validation studies. This study hopes to build a foundation for future digital phenotyping clustering work by scaling up to new sites, and populations to uncover the nature and extent of heterogeneity in schizophrenia.

Indexed as

SchizophreniaAdultCognitionCohort StudiesFemaleHumansMaleMiddle AgedPhenotypePsychiatric Status Rating ScalesPsychotic DisordersSchizophrenic PsychologySmartphone

Identifiers

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Registered trials

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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.