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  3. Efficacy and Safety of Anthocyanin-Rich Extract in Patients with Ulcerative Colitis: A Randomized Controlled Trial.
 

Efficacy and Safety of Anthocyanin-Rich Extract in Patients with Ulcerative Colitis: A Randomized Controlled Trial.

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BORIS DOI
10.48620/78781
Date of Publication
December 4, 2024
Publication Type
Article
Division/Institute

Clinic of Visceral Su...

Contributor
Biedermann, Luc
Doulberis, Michael
Schreiner, Philipp
Nielsen, Ole Haagen
The, Frans Olivier
Brand, Stephan
Burk, Sabine
Hruz, Petr
Juillerat, Pascal
Krieger-Grübel, Claudia
Leu, Kristin
Leventhal, Gabriel E
Misselwitz, Benjamin
Clinic of Visceral Surgery and Medicine, Visceral and Transplant Surgery
Clinic of Visceral Surgery and Medicine, Gastroenterology
Scharl, Sylvie
Schoepfer, Alain
Seibold, Frank
Herfarth, Hans
Rogler, Gerhard
Subject(s)

600 - Technology::610...

Series
Nutrients
ISSN or ISBN (if monograph)
2072-6643
Publisher
MDPI
Language
English
Publisher DOI
10.3390/nu16234197
PubMed ID
39683589
Uncontrolled Keywords

anthocyanin-rich extr...

bilberries

complementary therapy...

inflammatory bowel di...

ulcerative colitis

Description
Background: 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. Methods: 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. Results: 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 (p = 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; p = 0.035). Serious adverse events were rare. Conclusions: 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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/194708
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nutrients-16-04197.pdftextAdobe PDF1.78 MBAttribution (CC BY 4.0)publishedOpen
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