Evidence map›Paper›PMID 42131342›Full record

ArticleFrontiers in immunology2026

ISPAD, bridging clinical expertise and AI for autoimmune-related pernicious anemia diagnosis.

Nora Boumela, Guillaume Cadiot, Farid Chaoui

Abstract read
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Article in Frontiers in immunology, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Nora BoumelaDepartment of Electronics, University of Batna 2, Batna, Algeria.
Guillaume CadiotHepato-Gastroenterology and Digestive Oncology Department, Reims University Hospital Center, Reims, France.
Farid ChaouiFaculty of Medicine, University of Algiers, Algiers, Algeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pernicious anemia (PA) is a severe clinical consequence of autoimmune gastritis. It results from immune-mediated damage to gastric parietal cells in the oxyntic mucosa. This process leads to intrinsic factor deficiency and subsequent vitamin B Methods: To address the intrinsic diagnostic uncertainty of PA-arising from heterogeneous, graded, and often discordant clinical, histological, immunological, and biochemical information-we developed ISPAD (Intelligent System for Pernicious Anemia Diagnosis), an explainable AI-based probabilistic framework to integrate this information, producing a probability estimate of pernicious anemia that reflects clinical reasoning rather than rigid diagnostic thresholds. Results: ISPAD was examined using a series of published diagnostically challenging cases reflecting real-world complexity. These cases included antibody assay interference, hemolysis-masked macrocytosis, seronegative presentations, and cancer-associated atrophy. Across cases, the system generated a continuous and adaptable probabilistic assessment of pernicious anemia. This assessment relied on dynamic, context-dependent integration of available information and illustrated the potential for formalizing complex diagnostic reasoning. Conclusion: ISPAD illustrates how explainable artificial intelligence can formalize expert reasoning in autoimmune-related pernicious anemia. By integrating heterogeneous and often discordant information into a transparent probabilistic framework, this proof-of-concept approach provides a structured approach to diagnostic reasoning, particularly in complex or atypical situations.

Indexed as

Anemia, PerniciousArtificial IntelligenceAutoimmune DiseasesDiagnosis, DifferentialFemaleHumansParietal Cells, GastricAI-assisted diagnosisB12 deficiencyfundic atrophyOLGA classificationpernicious anemia

Identifiers

PMID42131342
PMCPMC13162043

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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 Socratic graph.