Evidence map›Paper›PMID 42636434›Full record

ArticleJMIR AI2026

A Simplified Metric to Streamline Between-Group Fairness Assessment for Predictive Models: Algorithm Development and Evaluation Study.

Haoyuan Wang, Chuan Hong, Michael Pencina, Matthew Engelhard

Abstract read
In one paragraph

Article in JMIR AI, 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

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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.

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3 · Its place in the literature

Who cites it

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

4 authors.

Haoyuan WangDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, 2424 Erwin Rd, Durham, NC, 27705, United States, 1 919-613-3665.ORCID http://orcid.org/0009-0007-1175-6881
Chuan HongDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, 2424 Erwin Rd, Durham, NC, 27705, United States, 1 919-613-3665.ORCID http://orcid.org/0000-0001-7056-9559
Michael PencinaDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, 2424 Erwin Rd, Durham, NC, 27705, United States, 1 919-613-3665.ORCID http://orcid.org/0000-0002-1968-2641
Matthew EngelhardDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, 2424 Erwin Rd, Durham, NC, 27705, United States, 1 919-613-3665.ORCID http://orcid.org/0000-0003-4112-9639

Funding

Machine Learning Methods to Develop and Deploy Real-Time Risk Surveillance for Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder from the Electronic Health RecordK01MH127309 · NIMH · DUKE UNIVERSITY · PI Matthew Morrow Engelhard · 2022 to 2026
$842k
NIMH NIH HHS K01 MH127309
6 · The paper itself

Abstract

Background: Fairness evaluation is essential for trustworthy clinical risk prediction. However, existing fairness-oriented discrimination metrics either ignore cross-group comparisons or rely on exhaustive pairwise evaluations, making them difficult to interpret and impractical for model selection. Objective: This study aimed to develop and evaluate novel fairness-oriented discrimination metrics for clinical risk prediction that address limitations of within-group and pairwise cross-group approaches. Methods: We examined theoretical properties of existing U-statistic-based metrics, including concordance index (CI) and area under the receiver operating characteristic curve (AUC), when applied to subgroups. We highlighted the distinction between within-group discrimination (ranking within a subgroup) and group-level discrimination (ranking relative to the broader population). Building on this framework, we proposed group-level extensions of the CI and AUC that summarize subgroup-specific performance in a single interpretable measure. We then applied these metrics to the PREVENT (Predicting Risk of Cardiovascular Disease Events) equation, a recently developed model for atherosclerotic cardiovascular disease. Results: The traditional subgroup-specific CI and AUC captured within-group but not group-level discrimination, obscuring inequities in clinical decision-making. Existing cross-group approaches (eg, the xCI and xAUC metrics) addressed this limitation but became computationally and interpretively burdensome with multiple subgroups due to pairwise comparisons. Our proposed metrics provided a streamlined alternative, yielding 1 summary statistic per subgroup while retaining sensitivity to cross-group ranking disparities. Applied to PREVENT, these metrics revealed differences in subgroup performance not apparent from within-group evaluations. Conclusions: By distinguishing between within-group and group-level discrimination, our framework clarifies a common source of misinterpretation in fairness evaluation. The proposed group-level extensions of the CI and AUC provide practical, interpretable tools for evaluating fairness in clinical prediction models, enabling more transparent and equitable risk assessment.

Indexed as

algorithmscardiovascular risk predictionmachine learningperformance metricstrustworthy AI

Identifiers

PMID42636434
PMCPMC13502933

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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.