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Characterization of Immune Semaphorin in Non Alcoholic Fatty Liver Disease and NASH

Not Applicable
Completed
Conditions
Non Alcoholic Fatty Liver Disease
Interventions
Other: Evaluation of the staging of fibrosis liver
Other: Determine the expression level of semaphorin
Other: Determination of the composition of immunity cells
Registration Number
NCT02820285
Lead Sponsor
Centre Hospitalier Universitaire de Nice
Brief Summary

Recent epidemiological studies in France showed a high prevalence of obesity (14.5%) and its strong increase in the last 20 years. Among the many complications associated with obesity, liver complications (steatosis and steatohepatitis \[NASH\]) are among the most common. Semaphorins were described in the early 1990. More than 20 types of these proteins have been reported to date. These proteins were used for neural development. Since many functions have also been described. The semaphorins are involved in numerous physiological or physiopathological processes (cardiac morphogenesis, vascular growth, tumor progression), the regulation of immune cells and liver fibrosis. Preliminary studies have allowed to show that dendritic cells infiltrate adipose tissue and initiate the activation of T cells and inflammation. Immune semaphorin are new players in the regulation of inflammation and immune reactions.

The role of immune semaphorin in regulating inflammation in the two compartments (liver and adipose tissue) could be a crucial step that could lead to more severe liver damage. Its dysregulation could explain NASH injuries. The goal is to identify a new mode of regulation of cellular homeostasis in the fatty liver disease. These factors may serve as diagnostic markers or future therapeutic targets.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
148
Inclusion Criteria
  • Male and female aged 18-65 years
  • Patients with body mass index justifying a surgery for obesity (BMI ≥ 40 kg / m2 or BMI ≥ 35 kg / m2 with comorbidities)
  • Consumption of alcohol <20 g / d
  • Patients affiliated to a social security insurance
  • Patients who signed the informed consent
Exclusion Criteria
  • Hemochromatosis
  • Toxic hepatitis
  • Deficiency of alpha-1-antitrypsin
  • Wilson's disease
  • Liver Autoimmune disease (primary biliary cirrhosis, autoimmune hepatitis)
  • Hepatitis B, C
  • Drug-induced hepatitis
  • Presence of HIV status
  • Corticosteroids, amiodarone, valproic acid, tamoxifen, anti-inflammatory drugs, lipid lowering agents, testosterone agonists or beta-adrenergic antagonists, orlistat.
  • Pregnant or breastfeeding women
  • Incarcerated patients or patient under guardianship

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control patientsEvaluation of the staging of fibrosis liver-
Control patientsDetermine the expression level of semaphorin-
Patients with overweight, steatosis and steatohepatitisDetermination of the composition of immunity cells-
Patients with overweight, steatosis and steatohepatitisDetermine the expression level of semaphorin-
Morbid obese patientsEvaluation of the staging of fibrosis liver-
Morbid obese patientsDetermine the expression level of semaphorin-
Morbid obese patientsDetermination of the composition of immunity cells-
Control patientsDetermination of the composition of immunity cells-
Patients with overweight, steatosis and steatohepatitisEvaluation of the staging of fibrosis liver-
Primary Outcome Measures
NameTimeMethod
Determination of the composition of immunity cellsDay 0

The investigators determine the composition of immunity cells by Immunohistochemical and biochemical analyses (Western Blotting)

Evaluation of the staging of liver fibrosisDay 0

The investigators determine the stage of liver fibrosis by histological study of biopsies

Determination of the expression of level of semaphorinDay 0

The investigators determine by technic of Reverse Transcription Polymerase Chain Reaction (RT-PCR) the expression of level of semaphorin

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Service d'Hépato-Gastroentérologie - Hôpital de l'Archet

🇫🇷

Nice, France

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