nonalcoholic fatty liver disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: NAFLD patients Patients with a pathological diagnosis of NAFLD based on a liver biopsy within the past 8 weeks Patients from whom consent has been obtained to participate in this study, which has been approved by the ethics committee.
Exclusion criteria
Exclusion criteria: a. Patients who have any other liver disease, such as chronic hepatitis C, chronic hepatitis B (HBs-Ag-positive patients), autoimmune hepatitis, primary biliary cirrhosis, primary sclerosing cholangitis, 1-antitrypsin deficiency, Wilson disease, or alcohol-related liver disease b. Patients who have a serious hepatic dysfunction, liver failure (encephalopathy, ascites, ruptured varices, or hyperbilirubinemia) c. Patients who have a serious renal dysfunction d. Patients who have a serious cardiopulmonary dysfunction e. Pregnant women, parturient women, breast-feeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| We will conduct this study by performing fatty acid scintigraphy in NAFLD patients grouped according to the degree of histopathological progression in the liver and make comparisons between the degrees of BMIPP uptake in the various groups. | — |
Secondary
| Measure | Time frame |
|---|---|
| We will comprehensively analyze each factor involved in fatty acid metabolism in each group by using blood serum collected in the fasting state, after a meal, and during fatty acid scintigraphy, and liver tissue. Then we assess their relationships with the disease status. | — |
Countries
Japan
Contacts
National Center for Global Health and Medicine Department of Gastroenterology