Dietary Modulation of Intestinal Microbiota as Trigger of Liver Health: Role of Bile Acids - "A Diet for Liver Health" (ADLH)

August 15, 2023 updated by: RWTH Aachen University

Dietary Modulation of Intestinal Microbiota as Trigger of Liver Health: Role of Bile Acids - "A Diet for Liver Health (ADLH)"

Studies in recent years have demonstrated that the commensal intestinal flora (microbiome) plays a key role in the development of nonalcoholic steatohepatitis (NASH). An unfavourable microbiom can trigger disease development and progression. On the other hand, recent data show that modulation of the microbiom by a diet can prevent the developement of a NASH. Mechanisms of interaction between nutrition, microbiome, intestine and liver are largely unknown. In this research project, the effect of a fibre-rich oat bran on NASH will therefore be investigated. A better understanding of the interaction between diet, microbiome, intestine and liver could form the basis for new preventive therapies of NASH.

Study Overview

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

Interventional

Enrollment (Actual)

84

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Vienna, Austria
        • Medical University of Vienna
      • Aachen, Germany
        • University Hospital RWTH Aachen
      • Gothenburg, Sweden
        • Sahlgrenska University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 75 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Christian Trautwein, Prof. Dr., Uniklinik RWTH Aachen, Med. Klinik III

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 20, 2019

Primary Completion (Actual)

April 30, 2022

Study Completion (Actual)

April 30, 2022

Study Registration Dates

First Submitted

March 14, 2019

First Submitted That Met QC Criteria

March 29, 2019

First Posted (Actual)

April 1, 2019

Study Record Updates

Last Update Posted (Actual)

August 16, 2023

Last Update Submitted That Met QC Criteria

August 15, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 17-105

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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