Claudia Krieger-Grübel, Gerhard Rogler, Hans Herfarth, Frank Seibold, Alain Schoepfer, Sylvie Scharl, Benjamin Misselwitz, Gabriel E Leventhal, Kristin Leu, Luc Biedermann, Pascal Juillerat, Petr Hruz, Sabine Burk, Stephan Brand, Frans Olivier The, Ole Haagen Nielsen, Philipp Schreiner, Michael Doulberis
Journal: Nutrients 2024;16(23):4197
PMID: 39683589
Ulcerative colitis (UC) is a chronic, relapsing inflammatory bowel disease (IBD) that primarily affects young adults. Anthocyanins (ACs), which are naturally occurring pigments found in berries, red wine, and dark-coloured vegetables, are known for their antioxidant, anti-inflammatory, and other protective effects. This study evaluated the efficacy, safety, and tolerability of an anthocyanin-rich extract (ACRE) in patients with moderately active UC. The trial was a multi-centre, double-blind, placebo-controlled, parallel-group study. Participants were randomly assigned in a 2:1 ratio to either the ACRE or placebo group. Results showed that ACRE did not significantly improve clinical response at 8 weeks in patients with moderate-to-severe UC. However it should be noted that an unusually large number of individuals in the placebo group experienced clinical improvements. There was a significant reduction in faecal calprotectin (FC), a biomarker of intestinal inflammation. The authors concluded that while ACRE did not meet the primary endpoint, the reduction in FC suggests a potential therapeutic benefit in UC management that warrants further research.
Bilberries are effective in inducing clinical, endoscopic, and biochemical improvement in ulcerative colitis (UC) patients. The aim of this study was to investigate the efficacy of anthocyanin-rich extract (ACRE), the bioactive ingredient of bilberries, in a controlled clinical trial in moderate-to-severe UC. A multi-center, randomized, placebo-controlled, double-blind study with a parallel group was conducted. Initially, the study was planned for 100 patients; nevertheless, it prematurely ended due to COVID-19. Patients had moderate-to-severe active UC at screening (a Mayo score of 6-12, an endoscopic sub-score ≥ 2) and were randomized at baseline. The primary endpoint was a clinical response (week 8, a total Mayo score reduction ≥ 3 points). Fecal calprotectin (FC) and a centrally read endoscopic response were among the secondary endpoints. Out of 48 patients (6 Swiss centers), 34 were randomized. Eighteen ACRE and eight placebo patients could be analyzed (per protocol set). Half (9/18) of ACRE patients and 3/8 of placebo patients responded clinically ( = 0.278). An improvement in the Mayo score was observed in the ACRE arm (77.8% vs. 62.5% placebo). FC dropped from 1049 ± 1139 to 557 ± 756 μg/g for ACRE but not for the placebo group (947 ± 1039 to 1040 ± 1179; = 0.035). Serious adverse events were rare. ACRE treatment did not yield significant superiority to the placebo. Furthermore, the placebo response was unusually high. Moreover, there was a significant calprotectin decrease at the end of treatment, indicative of ACRE efficacy in UC.
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