Curr Opin Gastroenterol. 2022 Jul 1;38(4):382-387.doi: 10.1097/MOG.0000000000000847.

Nienke Z Borren ¹, Ashwin N Ananthakrishnan ²

Author information

¹Department of Gastroenterology & Hepatology, Erasmus University Medical Center, Rotterdam, the Netherlands.

²Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.

Abstract

Purpose of review: In this article, we provide an overview of studies examining multiomic profiling in various clinical scenarios in the management of inflammatory bowel diseases (IBDs).

Recent findings: IBD arises as a result of an interplay between genetic, environmental, microbial and immunologic perturbations. The access to high throughput technology as well as the decrease in costs associated with such studies has led to a growing wealth of literature examining the utility of single or multiomic profiles in the management of IBD. Such studies have commonly examined the genome (and less frequently the epigenome), transcriptome, metabolome, proteome and the gut microbial metagenome in the context of overall IBD status or specific clinical scenarios, including the disease progression or response to treatment. The findings have provided important insight into how each of these compartments reflect underlying disease pathophysiologic processes and, in turn, can influence stratification of patients for clinical management.

Summary: Multiomic profiling in IBD has the potential to advance the field of personalized precision medicine in the management of IBDs.