Present and future of endoscopy precision for inflammatory bowel disease

Several advanced imaging techniques are now available for endoscopists managing inflammatory bowel disease (IBD) patients. These tools, including dye-based and virtual chromoendoscopy, probe-based confocal laser endomicroscopy and endocytoscopy, are increasingly innovative applications in clinical practice. They allow for a more in-depth and refined evaluation of the mucosal and vascular bowel surface, getting closer to histology. They have demonstrated a remarkable ability in assessing intestinal inflammation, histologic remission, and predicting relapse and favorable long-term outcomes. In addition, the future application of molecular endoscopy to predict biological drug responses has yielded preliminary but encouraging results. Furthermore, these techniques are crucial in detecting and characterizing IBD-related dysplasia, assisting endoscopic mucosal resection and submucosal dissection towards a surgery-sparing approach. Artificial intelligence (AI) holds great potential in this promising landscape, as it can provide an objective and reproducible assessment of inflammation and dysplasia. Moreover, it can improve the prediction of outcomes and aid in subsequent therapeutic decision-making. This review aims to summarize the promising role of state-of-the-art advanced endoscopic techniques and related AI-enabled models for managing IBD, paving the way for precision medicine.

Automated summary

Several advanced imaging techniques, including dye-based and virtual chromoendoscopy, probe-based confocal laser endomicroscopy and endocytoscopy, have shown great potential in managing inflammatory bowel disease (IBD) patients. These techniques allow for a more precise evaluation of mucosal and vascular bowel surface, enabling better assessment of inflammation, predicting outcomes, and assisting in therapeutic decision-making. Artificial intelligence (AI) also plays a promising role in objective assessment and improving prediction of outcomes in IBD.