Evidence map›Paper›PMID 41743038›Full record

ArticleFrontiers in psychiatry2026

Patient complexity profiles in depression: a machine learning approach to personalized mental health.

Paula Dagnino, Matias Salinas, Rodrigo Salas

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Paula DagninoFacultad de Psicología y Humanidades, Universidad San Sebastián, Santiago, Chile.
Matias SalinasHealth Sciences and Engineering, Universidad de Valparaíso, Valparaíso, Chile.
Rodrigo SalasHealth Sciences and Engineering, Universidad de Valparaíso, Valparaíso, Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patient complexity in mental health varies substantially, yet treatment approaches often rely on standardized protocols. Identifying distinct complexity profiles may support stratified care and more personalized intervention planning in depression. Objective: To identify distinct patient complexity profiles in depression across sociodemographic, clinical, and psychosocial indicators and to evaluate their clinical relevance for personalized treatment planning. Methods: We analyzed complete-case data from 270 adults with major depression using a Knowledge Discovery in Databases framework. Twelve indicators were analyzed via Principal Component Analysis followed by K-means clustering. Robustness was evaluated using supervised validation with a Random Forest classifier and SHAP-based interpretability analysis. Between-profile comparisons were conducted, and expert clinicians evaluated clinical relevance. Results: Model selection supported a three-cluster solution (k = 3: Low-, Moderate-, and High-complexity profiles). The solution was validated using a Random Forest classifier with strong performance (accuracy = 0.91). Statistical comparisons showed that the Low-complexity profile (n = 100, 37.0%) was older and more often partnered and employed, with lower depressive symptoms and better personality functioning. The Moderate-complexity profile (n = 87, 32.2%) was younger, predominantly unpartnered, and had the lowest employment rate and medical comorbidity. The High-complexity profile (n = 83, 30.7%) showed the most severe presentation, characterized by higher depressive symptoms, greater childhood maltreatment, and impaired personality functioning. Clinical experts confirmed interpretability and suggested tailored strategies for each profile. Conclusions: Machine learning identified clinically meaningful patient complexity profiles with significant differences across multiple domains. These profiles provide a framework for stratified care and personalized intervention planning, moving beyond one-size-fits-all approaches.

Indexed as

depression complexity profilesexplainable AI for mental healthmachine learningpersonalized mental health treatmentprofile-based interventions

Identifiers

PMID41743038
PMCPMC12930347

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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.