NAFLD - Nonalcoholic Fatty Liver Disease, NASH - Nonalcoholic Steatohepatitis
Conditions
Brief summary
Non-alcoholic fatty liver disease (NAFLD) covers a spectrum from reversible hepatic steatosis to inflammation and fibrosis termed steatohepatitis (NASH) and cirrhosis. New evidence indicates that NAFLD is associated with development of heart failure, abnormal ventricular glucose and fatty acid (FA) utilisation and cardiosteatosis. The mechanisms behind cardiac involvement and the progression from NAFL to NASH are poorly understood but must include altered cardiac and intrahepatic lipid handling. In collaboration with renowned research groups from Oxford, Mayo Clinic and Copenhagen we plan comprehensive kinetic studies of heart and liver FA uptake and oxidation, ventricular function and substrate utilisation, and hepatic triglyceride (TG) secretion in order to assess mechanisms governing cardiac and hepatic lipid and glucose trafficking in subjects with NAFL and NASH and the relationship with heart function. In addition, we will assess skeletal muscle and adipose tissue enzyme activities, gene expression and protein concentrations in these subjects to define mechanisms involved in the cross-talk between heart, liver, muscle and adipose tissues. We will address these questions using innovative tracer techniques (11Cpalmitate, 11C acetate, 18FDG glucose PET tracers and TG tracers) in combination with hepatic vein catherisation to study cardiac and liver substrate trafficking, as well as NMR spectroscopy, echocardiography, muscle and fat biopsies in combination with state-of-the art muscle and adipose tissue enzyme kinetics, gene- and protein expression. Effects of acute exercise as well as GLP-1 agonist and SGLT-2 inhibitor treatment (alone and in combination) will be assessed. The overarching goals are to define abnormalities and differences between NAFLD and NASH in hepatic lipid (FA and TG) metabolism and to assess hepatic, adipose and skeletal muscle lipid and substrate utilisation.
Interventions
None listed
Sponsors
University of Aarhus
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
MALE
Age
40 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* • 8 obese subject men with NAFL (MR spectroskopi, fibro scanner) (BMI \> 30). * 8 obese subject men with NASH (MR spectroskopi, fibro scanner) (BMI \> 30). * age between 40-70 years Written consent before the start of the study
Exclusion criteria
* known current disease * Fixed medical drug consumption except antihypertensive drugs and statins. However, pause statins 3 weeks before the examination date * Blood donation within the last 3 months prior to the study * Participation in experiments involving radioactive isotopes within the last 3 months * Alcohol abuse (over 21 items per week for men and 14 for women) * Smoking * Weight over 130 kg * Cancer patients * Large intake of medication
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Effects of exercise on VLDL-TG metabolism in individuals with NAFL or NASH | 3 years | * VLDL-TG turnover (µmol/min) * To evaluate the acute effects of exercise on VLDL-TG secretion and clearance * To assess the uptake and cellular/intracellular regulation of FFA and VLDL-TG in fat and muscle tissue |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Compare the acute effects of exercise in individuals with NAFL or NASH | 3 years | Oxidation of VLDL-TG-FA(µmol/min) |
Countries
Denmark
Outcome results
None listed