A bibliometric review of explainable AI in diabetes risk prediction: Trends, gaps, and knowledge graph opportunities

Background Type 2 diabetes mellitus (T2DM) is one of the most pressing global public health challenges. Machine learning (ML) combined with Explainable Artificial Intelligence (XAI) is increasingly applied to T2DM risk prediction, yet, to the best of our knowledge, no systematic quantitative overview of this landscape has been conducted.

Methods We present a bibliometric analysis of 1,933 Scopus documents (collected 29 March 2026), employing keyword analysis, thematic clustering, and publication trend analysis.

Results The field grew substantially — from 35 documents (2020) to 828 documents (2025). SHAP (SHapley Additive exPlanations) and LIME are the most prevalent XAI methods; XGBoost and Random Forest dominate the ML landscape. KG/GNN (Knowledge Graph/Graph Neural Network) gap: only 7 of 1,933 documents (∼0.36%) — a 71:1 disparity versus the XAI group. A selective review of 15 highly cited papers confirmed that 0/15 studies combine all three components ML + XAI + KG in T2DM risk prediction.

Contribution This study identifies the clinical interpretability gap — where statistical explanations from SHAP/LIME are not connected to structured clinical pathways — as the central challenge of XAI in T2DM risk prediction, and proposes a three-layer conceptual framework integrating KG as a semantic layer to address it. The framework has direct implications for clinical decision support systems (CDSS) and population-level public health screening, where explainability aligned with medical reasoning is essential for responsible deployment. The study provides a transferable methodology and quantified research gap analysis to guide future work combining machine learning, XAI, and structured medical knowledge.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

The author(s) received no specific funding for this work.

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No IRB approval was required. This study is a bibliometric analysis of publicly available publication metadata retrieved from Scopus and does not involve human participants, identifiable data, specimens, or tissue.

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