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Molecular Investigation of Non Alcoholic Fatty Liver Diseases in Obese Patients

Conditions
Liver Disease
Interventions
Procedure: cholecystectomy or benign liver tumor removal
Procedure: Bariatric surgery
Registration Number
NCT00844779
Lead Sponsor
University Hospital, Strasbourg, France
Brief Summary

Non alcoholic fatty liver diseases (NAFLD) are represented by two main pathological conditions, hepatic steatosis (HS) and non alcoholic steatohepatitis (NASH), which are characterized by the accumulation of fat in the liver. The diagnosis of these two entities is achieved by histology and neither imaging nor biochemical markers are accurate enough to discriminate them. At the contrary of HS, NASH features hepatocyte necrosis, inflammation and fibrosis of variable intensity that could progress and ultimately evolve to cirrhosis. Therefore, it is important to distinguish between HS and NASH in order to treat the patients accordingly. In this study, the investigators aim to understand the molecular mechanisms that govern the transition from benign steatosis to complicated NASH. The investigators will analyze by "Q-RT-PCR" and "DNA microarray" technologies in the liver of obese patients, the expression of genes that are susceptible to be involved in the pathogenesis of NAFLD and identify the potential signaling pathways responsible for the progression of the disease.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
90
Inclusion Criteria
  • Group T(n=30): patient without central adiposity, without insulin resistance, operated for cholecystectomy or a benign liver tumor
  • Group A (n=30): patient with central adiposity, insulin resistance and hepatic steatosis (histology).
  • Group B (n=30): patient with central adiposity, insulin resistance and steatohepatitis ± hepatic fibrosis (histology).
Exclusion Criteria
  • viral or autoimmune hepatitis
  • hematochromatosis
  • alcohol consumption (> 20 g/24h women, >30 g/24h men)
  • type 1 diabetes
  • inflammation or infection before procedure
  • abnormal hemostasis or coagulation- pregnancy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Tcholecystectomy or benign liver tumor removal(n=30): without central adiposity, without insulin resistance, operated for cholecystectomy or a benign liver tumor.
BBariatric surgery(n=30): with central adiposity, insulin resistance and steatohepatitis ± hepatic fibrosis (histology).
ABariatric surgery(n=30): with central adiposity, insulin resistance and hepatic steatosis (histology).
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Service d'Hépato-Gastro-Entérologie - Nouvel Hôpital Civil

🇫🇷

Strasbourg, France

Service de Chirurgie Digestive et Endocrinienne - Nouvel Hôpital Civil

🇫🇷

Strasbourg, France

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