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A Data-Driven Approach to Quantifying Immune States in Sepsis
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Identifying sepsis susceptibility genes in post-surgical patients using an artificial intelligence approach.

Fernando Vaquerizo-Villar1,2,3, Tamara Hernandez-Beeftink4, María Heredia-Rodríguez5,6,7

  • 1Department of Anaesthesiology, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.

Frontiers in Medicine
|December 31, 2025
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Summary

This study used explainable AI with genome-wide association studies to find new genetic markers for post-surgical sepsis. Early detection of sepsis risk is improved by identifying key genes like PRIM2, SYNPR, and RBSN.

Keywords:
explainable artificial intelligence (XAI)genome-wide association study (GWAS)personalized medicinesepsissurgical patients

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Area of Science:

  • Genomics
  • Artificial Intelligence
  • Medical Diagnostics

Background:

  • Early sepsis detection is crucial for patient outcomes.
  • Genome-wide association studies (GWAS) have identified sepsis genetic variants but face challenges with patient heterogeneity and analysis methods.
  • This study focuses on identifying new sepsis susceptibility loci in post-surgical patients using an explainable AI (XAI) approach on GWAS data.

Purpose of the Study:

  • To identify novel sepsis susceptibility loci in post-surgical patients.
  • To apply an explainable artificial intelligence (XAI) methodology to GWAS data for sepsis prediction.
  • To prioritize genetic variants associated with post-operative sepsis.

Main Methods:

  • Performed GWAS on 750 post-operative sepsis patients and 3,500 controls.
  • Applied a novel XAI-based methodology to GWAS-derived single nucleotide polymorphisms (SNPs) for sepsis prediction.
  • Assessed functional and enrichment effects of top-ranked variants and associated genes.

Main Results:

  • The XAI-GWAS approach effectively predicted post-surgical sepsis.
  • Prioritized SNPs (e.g., rs17653532, rs1575081785, rs74707084) showed high contribution to sepsis prediction.
  • Discovered sepsis risk loci with functional implications in gene expression, DNA replication, signaling, cell proliferation, and cardiac function.

Conclusions:

  • The combination of GWAS and XAI identified loci associated with post-operative sepsis susceptibility.
  • Key genes (PRIM2, SYNPR, RBSN) identified through pre-operative tests can improve risk stratification and early sepsis detection.
  • Further validation in diverse cohorts is needed to confirm findings and improve patient outcomes.