Non-Alcoholic Fatty Liver Disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with non-alcoholic fatty liver disease through Fibroscam; both genders; aged between 18 and 65 years.
Exclusion criteria
Exclusion criteria: Patients with: another cause of hepatic steatosis (alcohol, virus, genetics) or advanced liver disease; chronic kidney disease thyroid diseases; cushing's syndrome; cancer; pregnant or lactating women; history of upper gastrointestinal surgery; use of medications for weight loss; report of sensitivity to coffee; consumption of more than 3 cups of coffee per day.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hepatic impairment, serum alanine aminotransferase (ALT), aspartate transaminase (AST), alkaline phosphatase (AF) and gamma glutamyl transpeptidase (GGT) levels are expected to be decreased, based on the finding of a variation of at least 5% in pre and post-intervention measurements.;It is expected that the liver's degree of stiffness will be reduced by examining the hepatic elastography, based on a variation of at least 1 level in the pre- and post-intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the behavior of the clinical indicators related to the glycidic profile, verified through serum glucose and fasting insulin levels and HOMA-ir calculation.;To evaluate the behavior of the clinical indicators related to the lipid profile, verified by serum levels of total cholesterol, low density lipoprotein (LDL), high density lipoprotein (HDL) and triglycerides (TG).;To evaluate the behavior of oxidative stress markers, verified by oxidative damage of lipoperoxidation (TBARS), antioxidant defenses (SOD, GPx) and total antioxidant potential of plasma (TRAP).;Evaluate the behavior of inflammation markers, verified through serum levels of interleukin-6 (IL-6).;To evaluate the behavior of the anthropometric parameters, verified through BMI and values of waist, abdominal, hip and neck circumference, and body fat percentage.;An increase in the beneficial bacterial population is expected, measured through the analysis of the intestinal microbiota profile present in the feces.;Genetic differences are expected in the clinical evolution of the disease, verified through the presence or not of the polymorphism in the PNPLA3 gene. | — |
Countries
Brazil
Contacts
Universidade Federal do Rio de Janeiro