ArticleCureus2025
Mental Illness Diagnostic Criteria Can Be Simplified With Higher Symptom Prevalence and Correlations: A Simulation Study.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Multi-modal deep learning model for bipolar depression adolescents with verbal auditory hallucinations.Frontiers in psychiatry · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction The diagnostic criteria of mental illnesses have been found to assign excessive weights to certain input symptoms, and several input symptoms may not be significantly associated with their diagnosis. This study aims to investigate whether we can use input symptoms assigned much weight to diagnose mental illnesses with similar diagnostic accuracy as using all input symptoms. Methods The symptoms of three mental conditions were simulated based on a published study: major depressive episodes, dysthymic disorder, and manic episodes. We simulated symptoms with 0.05, 0.1, 0.3, 0.5, or 0.7 prevalence and 0, 0.1, 0.4, 0.7, or 0.9 correlations. For each of the 25 combinations of symptom prevalence and correlations, we simulated 100,000 subjects, and diagnoses were made based on the Diagnostic and Statistical Manual of Mental Disorders, 4th edition, text revision. For each simulation, we used a decision tree model that used a symptom with the best diagnostic accuracy to separate a population into diseased and non-diseased groups. This model continued using other symptoms to further separate the groups into subgroups. This process was repeated until the diagnostic accuracy could not be improved based on cross-validation errors. All analyses were implemented with R (v4.2.3; R Development Core Team, Vienna, Austria) and RStudio (v2023.6.0.421; RStudio Team, Boston, MA). Results The diagnoses of major depressive episodes, dysthymic disorder, and manic episodes required 15, 11, and 14 symptoms, respectively. There were opportunities to use fewer symptoms to approximate the diagnoses with 92% or higher sensitivities and specificities with certain combinations of symptom prevalence and correlations. For major depressive episodes, using two symptoms ("Depressed mood" and "Loss of interest or pleasure in daily activities" for more than two weeks) in the major criteria could diagnose the condition, with 100% sensitivity and specificity in some circumstances. Occasionally, the diagnosis of dysthymic disorder might be used to approximate the diagnosis of major depressive episodes. Conclusion There may lie opportunities to screen or follow up the diagnosis of major depressive episodes, dysthymic disorder, and manic episodes using fewer input symptoms, with at least 92% sensitivities and specificities. These opportunities exist in various combinations of symptom prevalence and correlations. However, there is a lack of real-world data on psychiatric symptoms and interventions to take advantage of these opportunities.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.