炎症性肠病
蛋白质组学
溃疡性结肠炎
炎症性肠病
医学
组学
疾病
转录组
结肠炎
克罗恩病
病理
生物信息学
计算生物学
生物
内科学
基因
基因表达
生物化学
作者
Christina Plattner,Gregor Sturm,Anja A. Kuehl,Raja Atreya,Sandro Carollo,Raphael Gronauer,Dietmar Rieder,Michael Günther,Steffen Ormanns,Claudia Manzl,Stefan Wirtz,Asier Rabasco Meneghetti,Ahmed N. Hegazy,Jay V. Patankar,Zunamys I. Carrero,Markus F. Neurath,Jakob Nikolas Kather,Christoph Becker,Britta Siegmund,Zlatko Trajanoski
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2025-03-26
被引量:3
标识
DOI:10.1101/2025.03.26.645544
摘要
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 patients with IBD 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI