ArticleJAMIA open2025
A fair machine learning model to predict flares of systemic lupus erythematosus.
Article in JAMIA open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled 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.
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
5 citing papers in PubMed, 1 synthesis or guideline pooled it.
- The application of artificial intelligence in systemic lupus erythematosus: a bibliometric analysis of current trends and future directions.Frontiers in medicine · 2026Pooled it
- An explainable machine learning model for predicting in-hospital infection in patients with systemic lupus erythematosus.Renal failure · 2026Article
- An explainable hybrid SMPR-Net-XGBoost framework for automated lupus nephritis detection using medical image analysis.International urology and nephrology · 2026Article
- Artificial Intelligence and Machine Learning in Rheumatology and Systemic Inflammatory Diseases: From Pattern Recognition to Signal Analysis and Clinical Decision Support.Journal of clinical medicine · 2026Review
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that disproportionately affects women and racial/ethnic minority groups. Predicting disease flares is essential for improving patient outcomes, yet few studies integrate both clinical and social determinants of health (SDoH). We therefore developed FLAME ( Materials and Methods: We conducted a retrospective cohort study of 28 433 patients with SLE from the University of Florida Health (2011-2022), linked to 675 contextual-level SDoH variables. We used XGBoost and logistic regression models to predict 3-month flare risk, evaluating model performance using the area under the receiver operating characteristic (AUROC). We applied SHapley Additive exPlanations (SHAP) values and causal structure learning to identify key predictors. Fairness was assessed using the equality of opportunity metric, measured by the false-negative rate across racial/ethnic groups. Results: The FLAME model, incorporating clinical and contextual-level SDoH, achieved an AUROC of 0.66. The clinical-only model performed slightly better (AUROC of 0.67), while the SDoH-only model had lower performance (AUROC of 0.54). SHAP analysis identified headache, organic brain syndrome, and pyuria as key predictors. Causal learning revealed interactions between clinical factors and contextual-level SDoH. Fairness assessments showed no significant biases across groups. Discussion: FLAME offers a fair and interpretable approach to predicting SLE flares, providing meaningful insights that may guide future clinical interventions. Conclusions: FLAME shows promise as an EHR-based tool to support personalized, equitable, and holistic SLE care.
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.