Abstract

The proactive approach to Crohn’s disease (CD) management advocates moving toward algorithmic tight-control scenarios that are designed for each CD phenotype to guide remission induction, maintenance therapy, active monitoring, and multidisciplinary care to manage the complexities of each inflammatory bowel disease (IBD) patient. This requires accurate initial clinical, laboratory, radiological, endoscopic, and/or tissue diagnosis for proper phenotypic stratification of each CD patient. A substantial proportion of patients in symptomatic remission have been reported to demonstrate evidence of active disease, with elevated fecal calprotectin(FC) and C-reactive protein (CRP) levels as a hallmark for mucosal inflammation. Active mucosal inflammation, and elevated CRP and fecal calprotectin (FC) have been shown to be good predictors of clinical relapse, disease progression, and complications in IBD patients. The next frontier of treatment is personalized medicine or precision medicine to help solve the problem of IBD heterogeneity and variable responses to treatment. Personalized medicine has the potential to increase the efficacy and/or reduce potential adverse effects of treatment for each CD phenotype. However, there is currently an unmet need for better elucidation of the inflammatory biopathways and genetic signatures of each IBD phenotype, so personalized medicine can specifically target the underlying cause of the disease and provide maximal efficacy to each patient.

Highlights

  • Crohn’s disease (CD) is a chronic, immune-mediated inflammatory bowel disease (IBD) of unknown etiology marked by recurrent bouts of transmural inflammation that can affect the entire gastrointestinal tract (GIT) from the mouth to the anus, with the potential to cause significant physical and psychological morbidity [1]

  • CD has been treated with a “bottom-up” stepwise approach based on results from studies that used subjective, symptom-based disease activity indices like the Crohn’s disease activity index (CDAI)

  • ADA dosing based on fecal calprotectin (FC), C-reactive protein (CRP), and Mucosal healing

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Summary

Introduction

Crohn’s disease (CD) is a chronic, immune-mediated inflammatory bowel disease (IBD) of unknown etiology marked by recurrent bouts of transmural inflammation that can affect the entire gastrointestinal tract (GIT) from the mouth to the anus, with the potential to cause significant physical and psychological morbidity [1]. The “treat-to-target” or proactive approach is Biomedicines 2020, 8, 193 refining the goals of CD treatment by aiming to improve objective measurements of inflammation, including C-reactive protein (CRP) and fecal calprotectin (FC), in addition to patient-reported outcomes using disease activity indices biomarkers. Thistoapproach can enable physicians issue that(PROs), significant numbers of patients wereand failing to respond conventional pharmacological to make better-informed decisions to modify treatment as needed to achieve deepofremission, i.e., therapy [8]. This approach can enable physicians to make better-informed decisions to modify treatment as needed to achieve deep remission, i.e., clinical remission with mucosal healing [9]. CD and to make recommendations for the future of CD management

Natural History
Evidence for Top-Down Remission Induction in IBD
Proactive Optimization of CD Therapy with Tight Control
Objective
Fecal Calprotectin
Multifactorial Disease Activity Indices
Small-Bowel Cross-Sectional Assessment
Multidisciplinary Care
A Proactive Algorithmic Approach
Discussion
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