Evidence map›Paper›PMID 42784642›Full record

ArticlePLOS digital health2026

SYNERGY-VAE: An explainable generative deep learning framework for discovering depression subgroups from multimodal population health data.

Divya Sharma, Alice Rueda, Qiaowei Lin, Shakila Meshkat, Argyrios Perivolaris, Venkat Bhat

Abstract read
In one paragraph

Article in PLOS digital health, 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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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Divya SharmaDepartment of Mathematics and Statistics, York University, Toronto, Ontario, Canada.ORCID https://orcid.org/0009-0004-5022-697X
Alice RuedaAI for Mental Health Program, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Qiaowei LinAI for Mental Health Program, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Shakila MeshkatAI for Mental Health Program, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Argyrios PerivolarisAI for Mental Health Program, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.
Venkat BhatAI for Mental Health Program, St. Michael's Hospital, Unity Health Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression represents a complex, multifactorial disorder influenced by the interplay of biological, behavioral, and social determinants. While extensive health surveys, including the National Health and Nutrition Examination Survey (NHANES), gather comprehensive multidomain data, existing studies tend to analyze these domains independently, overlooking the potential to identify integrated, data-driven patterns of depression risk. We have developed SYNERGY-VAE, an interpretable and multimodal deep learning framework that is designed to identify latent health subgroups and facilitate the transparent prediction of depression risk, utilizing NHANES-derived multimodal data from a large analytic cohort that spans five distinct domains from 2005 to 2018. SYNERGY-VAE utilizes a variational autoencoder to learn a shared latent representation derived from five modalities of NHANES, specifically demographic, dietary, examination, laboratory, and questionnaire data. Clustering within this latent space revealed subpopulations exhibiting distinct health signatures. To enhance interpretability, we triangulated insights utilizing encoder weights, standardized mean differences, and permutation feature importance (PFI). Machine learning classifiers were trained within each cluster employing the top 30 PFI-ranked features, with performance evaluated through the receiver operating characteristic area under the curve (AUC) in a 70/30 train-test split. Three latent clusters emerged, each demonstrating markedly different observed prevalence rates of depression within the analytic sample, ranging from 6.8% to 10.9%. Cluster-specific models consistently surpassed pooled models in performance, with the highest predictive accuracy identified in Cluster 2 utilizing XGBoost (AUC = 0.839, 95% CI:0.804-0.874). The importance of features varied across clusters, indicating unique depression risk profiles specific to each subgroup. SYNERGY-VAE demonstrates the power of generative, explainable deep learning for the identification of latent health phenotypes, thereby furthering the objectives of precision mental health. By integrating high-dimensional, multimodal data and facilitating transparent subgroup discovery, our model may inform future stratified and context-aware screening research and contribute to precision psychiatry-oriented research in large health survey datasets.

Identifiers

PMID42784642
PMCPMC13606994

What Socratic holds

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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 Socratic graph.