SepsisFAT: The Role of Immune Semaphorins in NAFLD

Sponsor
University Hospital for Infectious Diseases, Croatia (Other)
Overall Status
Recruiting
CT.gov ID
NCT04573543
Collaborator
Croatian Science Foundation (Other)
160
1
17.9
8.9

Study Details

Study Description

Brief Summary

To goal is to identify semaphorins that are associated with NAFLD and to investigate their relationship with variable degrees of steatosis and fibrosis.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Evaluation of the degree of fibrosis and steatosis
  • Diagnostic Test: Screening for the components of metabolic syndrome
  • Diagnostic Test: Measurement of serum semaphorin concentrations
  • Diagnostic Test: Identification of semaphorin gene polymorphisms

Detailed Description

Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease associated with systemic changes in immune response. Semaphorins were recently recognized as one of the key regulators of immune responses; while some suppress immune cells activation, proliferation, and production of inflammatory cytokines, others stimulate immune responses. We have previously shown that semaphorins are associated with pathogenesis of viral hepatitis and progression of fibrosis. However, their role in NAFLD is unknown. The hypothesis of this project is that semaphorins are regulators of inflammation in patients with NAFLD. This study is designed as a prospective, non-interventional study. The main aims are: (1) to analyze serum concentration of semaphorins in patients with NAFLD; (2) to analyze tissue expression of semaphorins in patients with NAFLD; (3) to analyze semaphorin gene polymorphisms associated with NAFLD. Semaphorins could be a novel diagnostic and prognostic biomarker as well as targets for immune modulation.

Study Design

Study Type:
Observational
Anticipated Enrollment :
160 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
The Role of Immune Semaphorins in NAFLD
Actual Study Start Date :
Sep 1, 2020
Anticipated Primary Completion Date :
Sep 1, 2021
Anticipated Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Patients with Non-alcoholic fatty liver disease

120 patients diagnosed with NAFLD

Diagnostic Test: Evaluation of the degree of fibrosis and steatosis
The degree of steatosis will be estimated using the controlled attenuation parameter (CAP), a method for grading steatosis by measuring the degree of ultrasound attenuation by hepatic fat using a process based on simultaneous transient elastography (TE) which measures the degree of fibrosis.

Diagnostic Test: Screening for the components of metabolic syndrome
Anthropometric measures including body mass index (BMI), waist circumference (WC), waist hip ratio (WHR), and waist height ratio (WHtR) will be measured in all patients. Results of the routine laboratory tests as part of the standard diagnostic procedure will be collected: bilirubin, AST, ALT, GGT, ALP, albumins, WBC, neutrophil-to-lymphocyte ratio, hemoglobin, platelet count, fasting glucose, triglycerides, cholesterol, HDL and LDL. Non-invasive scores of steatosis/fibrosis will be calculated (APRI, FIB4, NAFLD score). Patients will be screened for the components of metabolic syndrome.

Diagnostic Test: Measurement of serum semaphorin concentrations
Semaphorin concentration will be measured in patient sera by ELISA.

Diagnostic Test: Identification of semaphorin gene polymorphisms
Semaphorin genes will be sequenced to identify semaphorin gene polymorphisms associated with NAFLD.

Controls

40 healthy controls

Diagnostic Test: Evaluation of the degree of fibrosis and steatosis
The degree of steatosis will be estimated using the controlled attenuation parameter (CAP), a method for grading steatosis by measuring the degree of ultrasound attenuation by hepatic fat using a process based on simultaneous transient elastography (TE) which measures the degree of fibrosis.

Diagnostic Test: Screening for the components of metabolic syndrome
Anthropometric measures including body mass index (BMI), waist circumference (WC), waist hip ratio (WHR), and waist height ratio (WHtR) will be measured in all patients. Results of the routine laboratory tests as part of the standard diagnostic procedure will be collected: bilirubin, AST, ALT, GGT, ALP, albumins, WBC, neutrophil-to-lymphocyte ratio, hemoglobin, platelet count, fasting glucose, triglycerides, cholesterol, HDL and LDL. Non-invasive scores of steatosis/fibrosis will be calculated (APRI, FIB4, NAFLD score). Patients will be screened for the components of metabolic syndrome.

Diagnostic Test: Measurement of serum semaphorin concentrations
Semaphorin concentration will be measured in patient sera by ELISA.

Diagnostic Test: Identification of semaphorin gene polymorphisms
Semaphorin genes will be sequenced to identify semaphorin gene polymorphisms associated with NAFLD.

Outcome Measures

Primary Outcome Measures

  1. Detection of semaphorins in patients with NAFLD [12 months]

    Measurement of semaphorins concentration in serum of patients with NAFLD by enzyme-linked immunosorbent assay (ELISA)

  2. Identification of semaphorin gene polymorphism in patients with NAFLD [12 months]

    Sequencing of semaphorin genes in patients with NAFLD using Sanger sequencing

Secondary Outcome Measures

  1. Staging of liver steatosis [12 months]

    The degree of steatosis will be estimated using the controlled attenuation parameter (CAP) in patients with NAFLD

  2. Staging of liver fibrosis [12 months]

    The stage of liver fibrosis will be assessed by transient elastography (TE) in patients with NAFLD

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients diagnosed with NAFLD according to current guidelines (AASLD, EASL)
Exclusion Criteria:
  • Immunosuppression

  • Malignancies

  • Autoimmune diseases

  • Pregnancy

  • HIV

  • Chronic viral hepatitis

  • Presence of other chronic liver disease (hemochromatosis, Wilson's disease, toxic hepatitis, deficiency of alpha-1-antitrypsin, liver autoimmune disease)

  • Consumption of alcohol > 20 g/day

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital for Infectious Diseases Zagreb Zagreb Croatia 10000

Sponsors and Collaborators

  • University Hospital for Infectious Diseases, Croatia
  • Croatian Science Foundation

Investigators

  • Principal Investigator: Neven Papic, MD, PhD, University Hospital for Infectious Diseases Zagreb

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital for Infectious Diseases, Croatia
ClinicalTrials.gov Identifier:
NCT04573543
Other Study ID Numbers:
  • UHID-05
First Posted:
Oct 5, 2020
Last Update Posted:
Oct 5, 2020
Last Verified:
Sep 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 5, 2020