| Literature DB >> 35150242 |
Padhmanand Sudhakar1, Dahham Alsoud1, Judith Wellens1, Sare Verstockt1, Kaline Arnauts1, Bram Verstockt1,2, Severine Vermeire1,2.
Abstract
Inflammatory bowel disease [IBD] has a multifactorial origin and originates from a complex interplay of environmental factors with the innate immune system at the intestinal epithelial interface in a genetically susceptible individual. All these factors make its aetiology intricate and largely unknown. Multi-omic datasets obtained from IBD patients are required to gain further insights into IBD biology. We here review the landscape of multi-omic data availability in IBD and identify barriers and gaps for future research. We also outline the various technical and non-technical factors that influence the utility and interpretability of multi-omic datasets and thereby the study design of any research project generating such datasets. Coordinated generation of multi-omic datasets and their systemic integration with clinical phenotypes and environmental exposures will not only enhance understanding of the fundamental mechanisms of IBD but also improve therapeutic strategies. Finally, we provide recommendations to enable and facilitate generation of multi-omic datasets.Entities:
Keywords: -omic datasets; IBD complexity; collaborative research; coordinated funding; exposome; sparsity; strategies tailored to IBD; validation
Mesh:
Year: 2022 PMID: 35150242 PMCID: PMC9426669 DOI: 10.1093/ecco-jcc/jjac027
Source DB: PubMed Journal: J Crohns Colitis ISSN: 1873-9946 Impact factor: 10.020