| Literature DB >> 33669579 |
Giuseppe Privitera1, Daniela Pugliese2, Gian Ludovico Rapaccini1,2, Antonio Gasbarrini1,2, Alessandro Armuzzi1,2, Luisa Guidi1,2.
Abstract
Inflammatory bowel diseases (IBD) are chronic conditions that primarily affect the gastrointestinal tract, with a complex pathogenesis; they are characterized by a significant heterogeneity of clinical presentations and of inflammatory pathways that sustain intestinal damage. After the introduction of the first biological therapies, the pipeline of therapies for IBD has been constantly expanding, and a significant number of new molecules is expected in the next few years. Evidence from clinical trials and real-life experiences has taught us that up to 40% of patients do not respond to a specific drug. Unfortunately, to date, clinicians lack a valid tool that can predict each patient's response to therapies and that could help them in choosing what drug to administer. Several candidate biomarkers have been investigated so far, with conflicting results: clinical, genetic, immunological, pharmacokinetic and microbial markers have been tested, but no ideal marker has been identified so far. Based on recent evidence, multiparametric models seemingly hold the greatest potential for predicting response to therapy. In this narrative review, we aim to summarize the current knowledge on predictors and early markers of response to biological therapies in IBD.Entities:
Keywords: biological therapy; biomarkers; inflammatory bowel disease; predictors
Year: 2021 PMID: 33669579 DOI: 10.3390/jcm10040853
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241