AI Article Synopsis

  • A randomized controlled trial was conducted to assess the effectiveness of Bifidobacterium longum 536 (BB536) for treating Japanese patients with active ulcerative colitis (UC).
  • A total of 56 patients participated, with 28 receiving BB536 and 28 receiving a placebo for 8 weeks, and the results indicated that 63% of BB536 patients achieved clinical remission compared to 52% of placebo patients, although the difference was not statistically significant.
  • The BB536 group experienced notable reductions in their UC disease activity index scores and endoscopic measures, demonstrating better outcomes than the placebo group, with minimal side effects reported.

Article Abstract

Background And Aim: We conducted a randomized, double-blinded, placebo-controlled trial to investigate the efficacy of Bifidobacterium longum 536 (BB536) supplementation for induction of remission in Japanese patients with active ulcerative colitis (UC).

Methods: Fifty-six patients with mild to moderate UC were enrolled. Three patients had pancolitis, 36 had left-sided colitis, and 17 had proctitis. Patients were randomly treated with 2-3 × 10(11) freeze-dried viable BB536 (28 patients) or placebo (28 patients) for 8 weeks.

Results: In total, 63% of patients receiving BB536 showed clinical remission (UC disease activity index [UCDAI] ≤2) at week 8 compared to 52% of those receiving placebo (P = 0.395). We observed a significant decrease of UCDAI scores (3.8 ± 0.4 at baseline to 2.6 ± 0.4 at week 8) in the BB536 group (P < 0.01), whereas there was no significant decrease in the placebo group (P = 0.88). There was also a significant decrease in the Rachmilewitz endoscopic index (EI) and the Mayo subscore at week 8 in the BB536 group, whereas there was no significant decrease in the placebo group. A single patient in the BB536 group complained of a mild side-effect, but no other adverse effects were observed.

Conclusion: Supplementation with BB536 was well tolerated and reduced UCDAI scores, EI and Mayo subscores after 8 weeks in Japanese patients with mild to moderately active UC.

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Source
http://dx.doi.org/10.1111/den.12553DOI Listing

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