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.