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

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Completed
CT.gov ID
NCT02820285
Collaborator
(none)
148
1
3
42.1
3.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Evaluation of the staging of fibrosis liver
  • Other: Determine the expression level of semaphorin
  • Other: Determination of the composition of immunity cells
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
148 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Characterization of Immune Semaphorin in Non Alcoholic Fatty Liver Disease and NASH
Study Start Date :
Mar 1, 2013
Actual Primary Completion Date :
Sep 1, 2016
Actual Study Completion Date :
Sep 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Other: Morbid obese patients

Other: Evaluation of the staging of fibrosis liver
The investigators will determine the severity of steatosis, inflammation and fibrosis by histological study of liver biopsies

Other: Determine the expression level of semaphorin
The investigators will determine the expression level (gene and protein) of immune semaphorin and their (s) receptor (s) in the liver and subcutaneous and visceral adipose tissue by RT-PCR,

Other: Determination of the composition of immunity cells
The investigators determine the composition of immunity cells by immunohistochemical and biochemical analyses (Western Blotting )

Other: Control patients

Other: Evaluation of the staging of fibrosis liver
The investigators will determine the severity of steatosis, inflammation and fibrosis by histological study of liver biopsies

Other: Determine the expression level of semaphorin
The investigators will determine the expression level (gene and protein) of immune semaphorin and their (s) receptor (s) in the liver and subcutaneous and visceral adipose tissue by RT-PCR,

Other: Determination of the composition of immunity cells
The investigators determine the composition of immunity cells by immunohistochemical and biochemical analyses (Western Blotting )

Other: Patients with overweight, steatosis and steatohepatitis

Other: Evaluation of the staging of fibrosis liver
The investigators will determine the severity of steatosis, inflammation and fibrosis by histological study of liver biopsies

Other: Determine the expression level of semaphorin
The investigators will determine the expression level (gene and protein) of immune semaphorin and their (s) receptor (s) in the liver and subcutaneous and visceral adipose tissue by RT-PCR,

Other: Determination of the composition of immunity cells
The investigators determine the composition of immunity cells by immunohistochemical and biochemical analyses (Western Blotting )

Outcome Measures

Primary Outcome Measures

  1. Evaluation of the staging of liver fibrosis [Day 0]

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

  2. Determination of the expression of level of semaphorin [Day 0]

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

  3. Determination of the composition of immunity cells [Day 0]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Morbid obese patients

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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service d'Hépato-Gastroentérologie - Hôpital de l'Archet Nice France 06003

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Albert TRAN, MDPhD, Centre Hospitalier Universitaire de Nice

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT02820285
Other Study ID Numbers:
  • 11-PP-10
First Posted:
Jun 30, 2016
Last Update Posted:
Oct 5, 2017
Last Verified:
Jun 1, 2016
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 5, 2017