- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03897218
Dietary Modulation of Intestinal Microbiota as Trigger of Liver Health: Role of Bile Acids - "A Diet for Liver Health" (ADLH)
Dietary Modulation of Intestinal Microbiota as Trigger of Liver Health: Role of Bile Acids - "A Diet for Liver Health (ADLH)"
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In recent years, the results of animal experiments and some human intervention studies indicate that the commensal intestinal flora (microbiome) plays a key role in the development of nonalcoholic steatohepatitis (NASH). An unfavourable composition of the microbiome can trigger disease development and progression. On the other hand, recent data show that modulation of the microbiome through diet, such as a high-fibre diet, can prevent the developement of a NASH. It has been shown that the uptake of fibre-rich oats reduces LDL and total cholesterol without altering the HDL cholesterol level. Indeed, the results of several human intervention studies suggest that a regular intake of oat flakes with prebiotic food supplements is sufficient to lower LDL and total cholesterol levels. In a small clinical trial it was also shown that an intake of oat bran with prebiotic food supplements in two servings per day was associated with a significant reduction in ALT and AST activity in the serum of overweight individuals with signs of altered liver function. In addition, the use of oat bran to influence postprandial glucose and insulin response and satiety was discussed.
However, the mechanisms underlying the positive effects of treatments with pro-, pre- or synbiotics are not yet fully understood and generally accepted therapeutic strategies are still lacking. The exact influence of a fibre-rich diet on intestinal microbiom and bile acid composition is not yet known. In the research project described, the effect of oat bran with prebiotic food supplements on NASH will be investigated and mechanisms of interaction between diet, microbiome, bile acids and liver will be uncovered. A better understanding of this interaction could form the basis for new preventive therapies of NASH.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Fatty liver disease diagnosed by sonography (steatosis hepatis grade II and III) and CAP measurement (> 280dB)
- compliance
Exclusion Criteria:
- Allergy to oats
- Alcohol intake of more than 30 g/d (men) or 20 g/d (women)
- Treatment with ursodeoxycholic acid (UDCA), vitamin E or other NASH drugs 3 months prior to randomization
- Hepatocellular carcinoma or non-hepatic malignancy within the last 5 years
- Evidence of cirrhosis of the liver (Child A, B, C) or a history of decompensation
- Liver diseases not related to NASH, including chronic viral hepatitis B/D or C, autoimmune hepatitis, Wilson's disease or clinically manifest iron overload (heterozygous HFE is permitted), cholestatic liver disease (PBC/PSC)
- Adiposity surgery in the last 5 years
- BMI <18.5 kg / m2
- Liver transplantation
- Fibroscan> 12 kPa (patients with liver cirrhosis)
- Lack of CAP and ultrasound evaluation
- Age > 75 years
- HIV infection
- Heart Failure (New York Heart Association Class III - IV)
- Myocardial infarction, unstable coronary artery disease, coronary artery intervention or stroke in the last 6 months
- Unstable COPD, chronic inflammatory bowel disease or rheumatoid arthritis
- Unstable renal failure (changes in serum creatinine > 50% in the last 3 months) or terminal renal failure requiring dialysis
- Uncontrolled hypertension (SBP / DBP> 180/90 despite therapy)
- Uncontrolled metabolic conditions (poorly controlled or decompensated diabetes mellitus, HbA1c >7.5%)
- Food allergies or intolerances that require strict adherence to a diet, such as lactose intolerance or celiac disease.
- Pregnancy or breastfeeding women (anamnesis)
- Treatment with drugs or substances that can induce secondary NASH (e.g., tamoxifen, corticosteroids, amiodarone, methotrexate) or alleviate NASH (TNF antagonists) (e.g. metformin)
- Use of herbal food supplements
- Any participant who has taken antibiotics 6 weeks prior to the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Group 1
Patients consuming placebo (millet flakes) each day
|
The study participants should consume the prescribed amount of the study product every day.
The intake should be divided into 1-2 meals.
It is not necessary to limit or change normal eating habits.
|
|
Experimental: Group 2
Patients consuming oatmeal flakes with a low dosage of prebiotic food supplements
|
The study participants should consume the prescribed amount of the study product every day.
The intake should be divided into 1-2 meals.
It is not necessary to limit or change normal eating habits.
|
|
Experimental: Group 3
Patients consuming oatmeal flakes with a high dosage of prebiotic food supplements
|
The study participants should consume the prescribed amount of the study product every day.
The intake should be divided into 1-2 meals.
It is not necessary to limit or change normal eating habits.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of the influence of a dietary supplement in oat bran on the course of disease in the early stages of NASH by CAP (Controlled Attenuation Parameter) measurement to determine liver steatosis.
Time Frame: 20 weeks
|
CAP measurement (dB/m)
|
20 weeks
|
|
Evaluation of the influence of a dietary supplement in oat bran on the course of disease in the early stages of NASH by determination ALT-concentration in blood samples.
Time Frame: 20 weeks
|
Determination of ALT concentration (U/l) in blood samples
|
20 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Influence of dietary supplement in oat bran on concentration of AST
Time Frame: 20 weeks
|
Determination of AST concentration (U/l) in blood samples
|
20 weeks
|
|
Influence of dietary supplement in oat bran on the concentration of gamma-GT
Time Frame: 20 weeks
|
Determination of gamma-GT concentration (U/l) in blood samples
|
20 weeks
|
|
Influence of dietary supplement in oat bran on liver steatosis
Time Frame: 20 weeks
|
Sonography - Performing an abdominal ultrasound examination to detect liver steatosis
|
20 weeks
|
|
Influence of dietary supplement in oat bran on bile acid metabolism
Time Frame: 20 weeks
|
Determination of bile acid composition in stool samples
|
20 weeks
|
|
Influence of dietary supplement in oat bran on the composition of the intestinal microbiome
Time Frame: 20 weeks
|
Determination of microbiom in stool samples (bacterial DNA and RNA are isolated from the stool to determine the microbial composition)
|
20 weeks
|
|
Influence of dietary supplement in oat bran on intestinal permeability marker like citrullin
Time Frame: 20 weeks
|
Determination of intestinal permeability marker like citrullin (µmol/l)
|
20 weeks
|
|
Influence of dietary supplement in oat bran on metabolic markers
Time Frame: 20 weeks
|
Determination of concentration of diffenrent, previously not defined metabolic markers in blood samples by untargeted metabolomics analysis
|
20 weeks
|
|
Influence of dietary supplement in oat bran on inflammatory markers of NASH
Time Frame: 20 weeks
|
Determination of concentration of previously not defined inflammatory markers of NASH in blood samples by multiplex assays
|
20 weeks
|
|
Influence of dietary supplement in oat bran on blood pressure
Time Frame: 20 weeks
|
Measurement of blood pressure (mmHg)
|
20 weeks
|
|
Assessment of quality of life
Time Frame: 20 weeks
|
Questionnaires to evaluate quality of life: EQ-5D-5L EQ-5D questionnaires with 5-point Likert scale: "having no problems", "having slight problems", "having moderate problems", "having severe problems" & "being unable to do/having extreme problems" (the answers euquals 1-5 points, with 5 points beeing the worst outcome)
|
20 weeks
|
|
Assessment of the feeling of satiety/gastrointestinal symptoms
Time Frame: 20 weeks
|
Questionnaire "Structured Assessment of Gastrointestinal Symptoms" (SAGIS): 5-point Likert scale from no problem, mild, moderate, severe and very severe problem (0-4 points; 4 points equals "very severe problem" |
20 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Christian Trautwein, Prof. Dr., Uniklinik RWTH Aachen, Med. Klinik III
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-105
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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