Evidence map›Paper›PMID 38963925›Full record

ArticleJMIR mental health2024

Bayesian Networks for Prescreening in Depression: Algorithm Development and Validation.

Eduardo Maekawa, Eoin Martino Grua, Carina Akemi Nakamura, Marcia Scazufca, Ricardo Araya, Tim Peters, Pepijn van de Ven

Abstract read
In one paragraph

Article in JMIR mental health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  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

7 authors.

Eduardo MaekawaDepartment of Electronic and Computer Engineering, University of Limerick, Limerick, Ireland.ORCID 0009-0006-6657-9678
Eoin Martino GruaDepartment of Electronic and Computer Engineering, University of Limerick, Limerick, Ireland.ORCID 0000-0002-5471-4338
Carina Akemi NakamuraDepartamento de Psiquiatria, Faculdade de Medicina da Universidade de Sao Paulo, Universidade de Sao Paulo, Sao Paulo, Brazil.ORCID 0000-0002-4761-4486
Marcia ScazufcaDepartamento de Psiquiatria, Faculdade de Medicina da Universidade de Sao Paulo, Universidade de Sao Paulo, Sao Paulo, Brazil.ORCID 0000-0002-4545-006X
Ricardo ArayaCentre for Global Mental Health, King's College London, London, United Kingdom.ORCID 0000-0002-0420-5148
Tim PetersBristol Dental School, University of Bristol, Bristol, United Kingdom.ORCID 0000-0003-2881-4180
Pepijn van de VenDepartment of Electronic and Computer Engineering, University of Limerick, Limerick, Ireland.ORCID 0000-0003-3321-450X

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundIdentifying individuals with depressive symptomatology (DS) promptly and effectively is of paramount importance for providing timely treatment. Machine learning models have shown promise in this area; however, studies often fall short in demonstrating the practical benefits of using these models and fail to provide tangible real-world applications.

objectiveThis study aims to establish a novel methodology for identifying individuals likely to exhibit DS, identify the most influential features in a more explainable way via probabilistic measures, and propose tools that can be used in real-world applications.

methodsThe study used 3 data sets: PROACTIVE, the Brazilian National Health Survey (Pesquisa Nacional de Saúde [PNS]) 2013, and PNS 2019, comprising sociodemographic and health-related features. A Bayesian network was used for feature selection. Selected features were then used to train machine learning models to predict DS, operationalized as a score of ≥10 on the 9-item Patient Health Questionnaire. The study also analyzed the impact of varying sensitivity rates on the reduction of screening interviews compared to a random approach.

resultsThe methodology allows the users to make an informed trade-off among sensitivity, specificity, and a reduction in the number of interviews. At the thresholds of 0.444, 0.412, and 0.472, determined by maximizing the Youden index, the models achieved sensitivities of 0.717, 0.741, and 0.718, and specificities of 0.644, 0.737, and 0.766 for PROACTIVE, PNS 2013, and PNS 2019, respectively. The area under the receiver operating characteristic curve was 0.736, 0.801, and 0.809 for these 3 data sets, respectively. For the PROACTIVE data set, the most influential features identified were postural balance, shortness of breath, and how old people feel they are. In the PNS 2013 data set, the features were the ability to do usual activities, chest pain, sleep problems, and chronic back problems. The PNS 2019 data set shared 3 of the most influential features with the PNS 2013 data set. However, the difference was the replacement of chronic back problems with verbal abuse. It is important to note that the features contained in the PNS data sets differ from those found in the PROACTIVE data set. An empirical analysis demonstrated that using the proposed model led to a potential reduction in screening interviews of up to 52% while maintaining a sensitivity of 0.80.

conclusionsThis study developed a novel methodology for identifying individuals with DS, demonstrating the utility of using Bayesian networks to identify the most significant features. Moreover, this approach has the potential to substantially reduce the number of screening interviews while maintaining high sensitivity, thereby facilitating improved early identification and intervention strategies for individuals experiencing DS.

Indexed as

AlgorithmsBayes TheoremDepressionAdultBrazilFemaleHealth SurveysHumansMachine LearningMaleMass ScreeningMiddle AgedSensitivity and SpecificityAIanxietyartificial intelligenceBayesian networkdepressiondepressive symptomdigital mental healtheHealthmachine learningmachine learning modelmental healthmHealthmobile healthmoodmood disordermood disorderspatientpatient screeningpredictionprediction modelingprobabilistic machine learningsocioeconomic data setsstochastic gradient descentsurveytarget depressive symptomatologytelehealthutilization

Identifiers

PMID38963925
PMCPMC11258528

What OpenQuestion holds

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LicenceCC BY
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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.