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IBDome: an integrated molecular, histopathological, and clinical atlas of inflammatory bowel diseases

Authors

  • C. Plattner
  • G. Sturm
  • A.A. Kühl
  • R. Atreya
  • S. Carollo
  • R. Gronauer
  • D. Rieder
  • M. Günther
  • S. Ormanns
  • C. Manzl
  • A.R. Meneghetti
  • A.N. Hegazy
  • J. Patankar
  • Z.I. Carrero
  • M.F. Neurath
  • J.N. Kather
  • C. Becker
  • B. Siegmund
  • Z. Trajanoski

Journal

  • bioRxiv

Citation

  • bioRxiv

Abstract

  • Multi-omic and multimodal datasets with detailed clinical annotations offer significant potential to advance our understanding of inflammatory bowel diseases (IBD), refine diagnostics, and enable personalized therapeutic strategies. In this multi-cohort study, we performed an extensive multi-omic and multimodal analysis of 1,002 clinically annotated IBD patients and non-IBD controls, incorporating whole-exome and RNA sequencing of normal and inflamed gut tissues, serum proteomics, and histopathological assessments from images of H&E-stained tissue sections. Transcriptomic profiles of normal and inflamed tissues revealed distinct site-specific inflammatory signatures in Crohn’s disease (CD) and ulcerative colitis (UC). Leveraging serum proteomics, we developed an inflammatory protein severity signature that reflects underlying intestinal molecular inflammation. Furthermore, foundation model-based deep learning accurately predicted histologic disease activity scores from images of H&E-stained intestinal tissue sections, offering a robust tool for clinical evaluation. Our integrative analysis highlights the potential of combining multi-omics and advanced computational approaches to improve our understanding and management of IBD.


DOI

doi:10.1101/2025.03.26.645544