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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03080129
Other study ID # SAR
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 11, 2017
Est. completion date December 2026

Study information

Verified date August 2023
Source Medical University of Graz
Contact Vanessa Stadlbauer-Köllner, AssocProf Dr
Phone +4331638582282
Email vanessa.stadlbauer@medunigraz.at
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Protein-energy malnutrition (PEM) occurs in 65-90% of patients with liver cirrhosis. Severity of malnutrition correlates with progression of liver disease and leads to sarcopenia in 30-70% of cirrhotic patients. Malnutrition and sarcopenia are associated with an increased risk of complications and mortality. In cirrhosis the gut microbiome is altered leading to increased gut permeability, bacterial translocation and inflammation. Since the microbiome is involved in nutrient uptake and metabolism, it is hypothesized that microbiome alterations contribute to sarcopenia. A prospective controlled cohort study to investigate the interrelation of microbiome changes and sarcopenia in cirrhosis will be conducted. Furthermore the effect of nutritional interventions on the microbiome in cirrhosis will be studied. From this study information on how the gut microbiome composition and sarcopenia are associated in cirrhosis and if modulation of the gut microbiome by nutritional interventions is feasible will be collected.


Description:

Scientific background Protein-energy malnutrition (PEM) occurs in 65-90% of patients with chronic liver disease. PEM is caused by various factors including poor dietary intake, loss of appetite, decreased hepatic protein synthesis, malabsorption and hypermetabolism. It is associated with an increased risk of complications including ascites, hepatic encephalopathy, variceal bleeding, hepatorenal syndrome and mortality. There is a direct relation between the progression of the liver disease and the severity of malnutrition. Malnutrition and sarcopenia in liver cirrhosis patients PEM leads to sarcopenia as a common, but frequently overlooked, complication. Sarcopenia is defined as a decrease in muscle mass two standard deviations below the healthy young adult mean. Sarcopenia is associated with aging, chronic diseases and malignancy. To determine the severity of muscle wasting, computed tomography scan (CT) or magnetic resonance imaging (MRI) are an objective and reproducible technique. Sarcopenia negatively impacts on survival, correlates with the risk of infections, increases surgical risk and leads to a poor quality of life. Besides PEM also inflammation is of importance in the development of sarcopenia. Diversity in the microbiome in patients with liver cirrhosis and association with sarcopenia. The gut microbiome of liver cirrhosis patients is altered compared to healthy individuals. Dysbiosis leads to an increased gut permeability, bacterial translocation and inflammation. This contributes to fibrogenesis and may also be related to hepatocarcinogenesis. Hence, new treatment approaches in cirrhosis focus on changing the microbial landscape. Modulation the gut microbiome may also be a strategy to reverse sarcopenia by reducing systematic inflammation. Hypothesis and aims There is an association between gut microbiome composition, gut permeability and the existence of sarcopenia in cirrhotic patients. Primary hypothesis: Diversity of the gut microbiome is reduced in liver cirrhosis patients with sarcopenia compared to those without sarcopenia or healthy controls. Secondary hypotheses: There is an association between gut microbiome composition, biomarker of gut permeability and bacterial translocation with the presence of sarcopenia in cirrhosis. Oral nutrition supplements (ONS) can influence the composition of the gut microbiome, gut permeability, bacterial translocation and inflammation. Sarcopenia can be diagnosed from patients portraits. Aims: to investigate: - the composition of the gut microbiome - biomarkers of gut permeability, bacterial translocation and inflammation - the incidence and severity of sarcopenia - the impact of oral nutrition supplements (ONS) on the gut microbiome - whether artificial intelligence can be used to diagnose sarcopenia from face portraits.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date December 2026
Est. primary completion date December 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Hospitalized patients for any reason with clinical/radiological/histological diagnosis of cirrhosis - Age >18y - Informed consent - CT/MRI scan within +/-14 days of the baseline study visit Exclusion Criteria: - Hepatic encephalopathy > grade 2 and or other cognitive disorder not allowing informed consent - advanced hepatocellular carcinoma - Any other condition or circumstance, which, in the opinion of the investigator, would affect the patient's ability to participate in the protocol

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Fresubin energy
dietary protein energy supplement

Locations

Country Name City State
Austria Medical University Graz Graz

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Graz

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Alpha diversity 16s rDNA sequencing of the stool microbiome day 1
Secondary Zonulin ELISA day 1
Secondary diamino-oxidase ELISA day 1, day 7
Secondary Calprotectin ELISA day 1
Secondary Gut permeability marker panel change between day 1 and day 7
Secondary taxonomic composition of the microbiome 16s rDNA sequencing of the stool microbiome day 1
Secondary taxonomic composition of the microbiome 16s rDNA sequencing of the stool microbiome change between day 1 and day 7
Secondary lipopolysaccharide HEK blue cell assay day 1
Secondary sCD14 ELISA day 1
Secondary lipopolysaccharide binding protein ELISA day 1
Secondary bacterial DNA HEK blue cell assay day 1
Secondary bacterial translocation marker panel change between day 1 and day 7
Secondary cytokine panel Bead array day 1
Secondary carboxylated proteins ELISA day 1
Secondary advanced oxidation end products ELISA day 1
Secondary inflammation marker panel change between day 1 and day 7
Secondary myostatin ELISA day 1
Secondary fibroblast growth factor 21 ELISA day 1
Secondary insulin like growth factor 1 ELISA day 1
Secondary Irisin ELISA day 1
Secondary nutritional status Questionnaire day 1
Secondary Sarcopenia MR/CT scan day 1
Secondary face portrait face portraits "selfies" will be obtained and AI algorithms will be used to diagnose sarcopenia from selfies day 1
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