Patients with fatty liver and type 2 diabates
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients whose BMI is more than 35 kg/m2 in operative group and more than 30 kg/m2 in control group 2) Patients who are 20-year-old or older 3) Patients suspected NASH/NAFLD 4) Patients who are able to understand the study and willing to provide written informed consent
Exclusion criteria
Exclusion criteria: 1) Patients who are deemed to be unsuitable by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of hepatic steatosis and fibrosis in the blood test and image examination | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Body weight, BMI and waist circumference 2) Total weight loss rate and excess weight loss rate 3) Blood pressure 4) Fasting plasma glucose 5) Adiponectin and reptin 6) Other blood and urine tests (liver, kidney, lipid, bone metabolism, nutrition, endocrine, etc) 7) Visceral fat mass and subcutaneous fat mass (HDS-2000 DUALSCAN) 8) Visceral fat mass and subcutaneous fat mass (computed tomography) 9) Body composition (InBody) 10) Dual-energy X-ray absorptiometry 11) Hepatic hepatosis and fibrosis index (calculation from blood tests) 12) Insulin kinetics with 75gOGTT 13) Liver biopsy | — |
Countries
Japan
Contacts
Hokkaido University Graduate School Department of Rheumatology, Endocrinology and Nephrology