Abstract

Several compounds based on short chain fatty acids and/or probiotics/prebiotics have shown promising results in the therapy of ulcerative colitis (UC), possibly due to its key role in restoring gut homeostasis as well as intestinal barrier integrity. Here, we investigated the efficacy of a patented preparation based on calcium butyrate, Bifidobacterium bifidum, Bifidobacterium lactis, and fructooligosaccharides (FEEDColon®, Princeps, Cuneo, Italy) in maintaining remission and improving subjective symptoms and inflammatory indices in patients with UC receiving 5-ASA therapy. A total of 42 patients were prospectively recruited and randomized in 21 patients receiving combination therapy with mesalamine (5-ASA) plus FEEDColon® and 21 patients treated with standard 5-ASA therapy. Patients were assessed at baseline, at 6-month, and 12-month follow-up (FU). Therapeutic success (defined as Mayo partial score ≤ 2 and faecal calprotectin (FC) < 250 µg/g at 12-month FU) was reached by 32 (76%) patients: 20 (95%) among those treated with 5-ASA + FeedColon®, and 12 (57%) among those treated with 5-ASA only (p = 0.009). Consistently, patients treated with combination therapy improved subjective symptoms (quality of life, abdominal pain, and stool consistency) and reduced FC values, while those treated with 5-ASA alone, improved neither subjective symptoms nor FC during the FU. In conclusion, FEEDColon® supplementation appears to be a valid add-on therapy for the maintenance of remission in patients with UC. Further multicentre, placebo-controlled, double-blind clinical trials are needed to validate our results on larger cohorts of patients with UC.

Highlights

  • IntroductionInflammatory bowel diseases (IBD) include Crohn’s disease (CD) and ulcerative colitis (UC), both characterized by a chronic–remittent clinical course [1]

  • Licensee MDPI, Basel, Switzerland.Inflammatory bowel diseases (IBD) include Crohn’s disease (CD) and ulcerative colitis (UC), both characterized by a chronic–remittent clinical course [1]

  • We recently showed that add-on therapy with microencapsulated-sodium-butyrate in patients with UC was effective in maintenance of clinical remission (83.3%) compared to those treated with mesalamine only (47.6%) [20]

Read more

Summary

Introduction

Inflammatory bowel diseases (IBD) include Crohn’s disease (CD) and ulcerative colitis (UC), both characterized by a chronic–remittent clinical course [1]. Compared to CD that can occur in any portion of the gastrointestinal tract, UC is limited to the colon [2]. The aetiology and pathogenesis of IBD are not fully understood; it is likely that different genetic and environmental factors [3,4,5,6], associated to an impaired intestinal permeability [7], are involved in the onset and progression of the disease. Interaction with the intestinal immune system may play a central role in triggering and exacerbating IBD [8,9]. Among the therapeutic armamentarium for the treatment of IBD, mesalamine (5-ASA)

Objectives
Methods
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call