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The Effect of Riboflavin in Crohn's Disease

The Effect of Riboflavin Supplementation on Faecalibacterium Prausnitzii in Crohn's Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02538354
Acronym
RISE-UP
Enrollment
70
Registered
2015-09-02
Start date
2016-03-31
Completion date
2017-04-30
Last updated
2020-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn Disease

Keywords

Riboflavin (vitamin B2), Faecalibacterium prausnitzii

Brief summary

This study will evaluate if suppelementation of the diet with riboflavin in Crohn's disease patients will result in an increase in the amount of F. prausnitzii.

Detailed description

Rationale Recent studies show that in patients with Inflammatory Bowel Disease (IBD) a dysbiosis exists in the composition of the intestinal microbiota. In particular, the potentially pathogenic bacterium Escherichia coli (E. coli) is often more abundant in the bowel of IBD patients, and the anaerobic commensal Faecalibacterium prausnitzii (F. prausnitzii) is often reduced. This last mentioned bacteria is known to be abundant in the intestine of healthy individuals. It is known to produce butyrate, which stimulates the intestinal epithelium, and to secrete anti-inflammatory substances. Riboflavin - also known as vitamin B2 - is required for a wide variety of cellular processes and has an important role in maintaining health in humans. In a pilot intervention with healthy volunteers it is shown that a riboflavin supplement increases the number of F. prausnitzii and results in a higher production of butyrate. In Crohn's disease patients, it is known that the amount of F. prausnitzii in the intestine is generally low. Furthermore, it is known that there is an association between the number of F. prausnitzii bacteria and the length of disease in remission. This study will evaluate if supplementation of the diet with riboflavin in Crohn's disease patients will result in a similar increase in the amount of F. prausnitzii as in healthy volunteers. In this patient group, an increase in the number of F. prausnitzii bacteria in the bowel may result in a more favourable disease course. This will be assessed with faeces calprotectin and two questionnaires. Additionally the investigators will assess if there is any modulation by riboflavin on the other intestinal bacteria, short chain fatty acids (SCFAs) (such as butyrate), and the pH of the faeces. Finally, the effect of the riboflavin on the permeability of the gut will be evaluated with a Chroom-EDTA test, and a number of different biomarkers of permeability. Hypothesis The hypothesis is that in Crohn's disease patients, supplementation of the diet with riboflavin results in an increase in the amount of F. prausnitzii, changes in microbial composition, increased fatty acid production, an increase in pH and a reduction of intestinal permeability. These changes might result in a more favourable disease course with less exacerbations. Study design Prospective clinical study. Study population and sample size In total 84 Crohn's disease patients will be included in this study, divided into two groups. Group 1 (n=42) will consist of patients with disease in remission (quiescent disease); group 2 (n=42) will consist of patients with active disease. In this study an adaptive design will be used. First 12 patients in the disease in remission group will be analysed. The methods of analysis and safety aspects will be taken into account. Intervention Supplementation of the normal diet with 1 capsule of 100 mg riboflavin (vitamin B2) during three weeks.

Interventions

DIETARY_SUPPLEMENTRiboflavin supplementation

Supplementation of the normal diet with 1 capsule of 100 mg riboflavin (vitamin B2) during three weeks

Sponsors

University Medical Center Groningen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Crohn's disease patients * Age 18-65 years * Concomitant medication for Crohn's disease is allowed in all groups

Exclusion criteria

* Swallowing disorders * Pregnancy and lactation * Use of antibiotic drugs, probiotics (i.e.Yakult, Vifit, Activia etc) or specific prebiotic supplements in the 3 weeks prior to the riboflavin intervention * Use of Methotrexate drugs * Colonoscopy and colon cleansing in last 3 months * Use of a vitamin B2 supplement, or multivitamin complexes containing vitamin B (i.e. vitamin B-complex) in the 3 weeks prior to the riboflavin intervention * Severe Crohn's disease (HBI \> 12)

Design outcomes

Primary

MeasureTime frameDescription
F. Prausnitzii (FISH Analysis).Different time points up to 6 weeks from start study: Day0, Day7, Day28The faeces is collected at different time points before and after riboflavin supplementation. To investigate the effect of a riboflavin supplement on the number of F. prausnitzii bacteria in the faeces of active and quiescent Crohn's disease patients.

Countries

Netherlands

Participant flow

Participants by arm

ArmCount
Riboflavin Supplementation in Quiescent Disease
Group 1 (n=42) will consist of patients with disease in remission (quiescent disease). Riboflavin supplementation: Supplementation of the normal diet with 1 capsule of 100 mg riboflavin (vitamin B2) during three weeks
40
Riboflavin Supplementation in Active Disease
Group 2 (n=42) will consist of patients with active disease. Riboflavin supplementation: Supplementation of the normal diet with 1 capsule of 100 mg riboflavin (vitamin B2) during three weeks
30
Total70

Baseline characteristics

CharacteristicRiboflavin Supplementation in Active DiseaseTotalRiboflavin Supplementation in Quiescent Disease
Age, Continuous38.8 years
STANDARD_DEVIATION 13.6
41.9 years
STANDARD_DEVIATION 12.7
44.2 years
STANDARD_DEVIATION 11.6
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
30 Participants70 Participants40 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants
Sex: Female, Male
Female
19 Participants48 Participants29 Participants
Sex: Female, Male
Male
11 Participants22 Participants11 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 400 / 30
other
Total, other adverse events
0 / 400 / 30
serious
Total, serious adverse events
0 / 400 / 30

Outcome results

Primary

F. Prausnitzii (FISH Analysis).

The faeces is collected at different time points before and after riboflavin supplementation. To investigate the effect of a riboflavin supplement on the number of F. prausnitzii bacteria in the faeces of active and quiescent Crohn's disease patients.

Time frame: Different time points up to 6 weeks from start study: Day0, Day7, Day28

ArmMeasureGroupValue (MEDIAN)
Riboflavin Supplementation in Quiescent DiseaseF. Prausnitzii (FISH Analysis).T0 (Mean of Day 0 and Day 7 combined)4.53 Relative FISH counts from total bacteria
Riboflavin Supplementation in Quiescent DiseaseF. Prausnitzii (FISH Analysis).T3 (Day 28)6.19 Relative FISH counts from total bacteria
Riboflavin Supplementation in Active DiseaseF. Prausnitzii (FISH Analysis).T0 (Mean of Day 0 and Day 7 combined)5.07 Relative FISH counts from total bacteria
Riboflavin Supplementation in Active DiseaseF. Prausnitzii (FISH Analysis).T3 (Day 28)5.46 Relative FISH counts from total bacteria

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026