Assessing the Severity of Metabolic-related Liver Injuries in Aging HIV-monoinfected Patients (ANRS ECHAM)
Primary Purpose
HIV Infection, Liver Injuries
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
MRI and biopsy
Sponsored by

About this trial
This is an interventional diagnostic trial for HIV Infection
Eligibility Criteria
Inclusion Criteria:
- Age ≥40 years
- Infection with HIV-1
- Cumulative exposure to cART for at least 5 years and currently under cART
- Viral load < 400 copies/mL
- CD4 count > 100 CD4/mm3
Female may be eligible to enter and participate in the study if she:
- is of non-child-bearing potential defined as either post-menopausal (12 months of spontaneous amenorrhea and ≥45 years of age) or physically incapable of becoming pregnant with documented tubal ligation, hysterectomy or bilateral oophorectomy or
- is of child-bearing potential with a negative blood pregnancy test at screening visit
- Informed consent signed prior to any study procedure
- To be covered by a medical insurance (only for French centres)
Presence of:
the metabolic syndrome as defined by the most recent international consensus definition (Alberti et al. Circulation 2009) including three components among the following criteria:
- visceral obesity (waist circumference: Europeans and Africans ≥ 94 cm for men and ≥ 80 cm for women, Americans ≥ 102 cm for men and ≥ 88 cm for women, Asians ≥ 90 cm for men and ≥ 80 cm for women)
- blood glucose ≥ 1 g/L (5,6 mmol/L) or anti-diabetic treatment,
- serum triglycerides ≥ 1,5 g/L (1,7 mmol/L) or hypertriglycerides treatment,
- serum HDL cholesterol < 0,4 g/L (1 mmol/L) for men and < 0,5 g/L (1,3 mmol/L) for women or hypercholesterolemia treatment,
- blood pressure (Diastolic ≥130 mmHg and/or Systolic ≥ 85 mmHg) or antihypertensive treatment
- and/or clinical lipoatrophy and/or lipohypertrophy using clinical questionnaires used and validated in previous published studies (ANRS 121 Hippocampe trial),
- and/or chronic elevated transaminases ≥ 1.5 ULN and / or GGT ≥ 2 ULN confirmed by two blood samples within at least three-month interval over twelve months prior screening visit.
Exclusion Criteria:
- Coinfection with hepatitis B (positive HBs antigen or isolated positive HBc antibody with positive PCR)
- Positive HCV serology
- Coinfection HIV-1 and HIV-2
- Use of intravenous drugs within the last six months
- Excessive alcohol intake (male > 50 g/d, female > 40 g/d)
- Other causes of liver diseases i.e: viral hepatitis, hemochromatosis, Wilson disease, autoimmune hepatitis, primary or secondary biliary cirrhosis, primary or secondary cholangitis, α1 antitrypsine deficiency
- Other causes of liver steatosis: current steroid therapy, current therapy with amiodarone, tamoxifen, methotrexate, nifedipine, or hycanthone; history of cancer chemotherapy; short bowel syndrome, polycystic ovarian syndrome, Weber-Christian disease
- Active opportunistic infection except for candida oesophagitis
- Current Cancer
- Pregnancy
- Decompensated heart failure
- Subject under legal guardianship
- Inability to give informed consent or incapacitation
- Contra-indication to MRI: pace-maker, neurovascular surgery, intraocular materials, cochlear implant, severe claustrophobia
- Participation in another study with an ongoing exclusion period at screening
Sites / Locations
- CHU Brussels
- Hôpital la Salpêtrière
- Hôpital Saint Antoine
- Medical Center for Infectious Diseases
- Center for HIV and Hepato-Gastroenterology
- University Medical Center
- Hannover Medical School
Outcomes
Primary Outcome Measures
Percentage of steatosis detected by MRI
Secondary Outcome Measures
Percentage of fibrosis or cirrhosis using non invasive markers and concordance of non invasive markers
Risk factors (age, duration of infection, treatment, clinical and biological metabolic and adipose tissue parameters) of liver injuries
Independent risk factors of NAFLD, NASH and fibrosis (including markers of insulin resistance, inflammatory cytokines, markers of immune activation, adipokines)
Establish a diagnosis score based on biomarkers of liver injuries (Adiponectin, leptin, IL6, CRP, CD14)
Quantifiable levels of serum adiponectin, serum leptin, serum HS-IL-6, HS-CRP, serum s-CD14 will be measured.
Description of pathogenetic factors and correlates with autophagy in liver biopsies of patients with evidence for liver fibrosis
Autophagosome formation in the liver biopsies (only for patients presenting liver fibrosis equal or > 2 will be quantified.
Identification of features of the adaptive immune system associated to NAFLD, NASH and fibrosis (T cell activation, surface expression of Treg, NK cells, NKT cells)
Quantifiable levels of T cell activation (in PBMC), Frequency and phenotype of Tregs (in PBMC), Quantifiable levels of NK cells (in PBMC), Quantifiable levels of Th17 and γδ T cell (in PBMC), Quantifiable levels of Plasma LPS and LPB (sCD163, CD26, Cytokeratin 18) will be measured.
Impact of IL28B and PNPLA3 genetic polymorphisms on the severity of liver steatosis, inflammation and fibrosis
Percentage of patients with NASH, fibrosis and cirrhosis on liver biopsy
Full Information
NCT ID
NCT02093754
First Posted
January 17, 2014
Last Updated
July 11, 2016
Sponsor
ANRS, Emerging Infectious Diseases
1. Study Identification
Unique Protocol Identification Number
NCT02093754
Brief Title
Assessing the Severity of Metabolic-related Liver Injuries in Aging HIV-monoinfected Patients
Acronym
ANRS ECHAM
Official Title
Assessing the Severity of Metabolic-related Liver Injuries in Aging HIV-monoinfected Patients: a European Multicentre Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
May 2014 (undefined)
Primary Completion Date
March 2016 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ANRS, Emerging Infectious Diseases
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will allow to assess liver related injuries in HIV patients.
Detailed Description
This study is a cross-sectional, multicentre study including 7 centres from 3 European countries (Belgium, France, Germany).
The maximum duration of the study for each patient will be 4 months, consisting of:
a screening visit,
an inclusion visit to perform the biologic tests and exams necessary for the study, within 1 month after the screening visit,
a result delivery visit within 1 month after inclusion visit, to disclose results of previous investigations. Patients with one or two non invasive markers suggesting significant fibrosis (≥F2) will be invited for liver biopsy within the next 2 months.
a "liver biopsy" visit, within 2 months after visit 2, liver biopsy in selected and consented patients
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection, Liver Injuries
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
460 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
MRI and biopsy
Primary Outcome Measure Information:
Title
Percentage of steatosis detected by MRI
Time Frame
Within 6 months after all patients have completed MRI
Secondary Outcome Measure Information:
Title
Percentage of fibrosis or cirrhosis using non invasive markers and concordance of non invasive markers
Time Frame
Within 6 months after all patients have completed the study
Title
Risk factors (age, duration of infection, treatment, clinical and biological metabolic and adipose tissue parameters) of liver injuries
Time Frame
Within 6 months after all patients have completed the study
Title
Independent risk factors of NAFLD, NASH and fibrosis (including markers of insulin resistance, inflammatory cytokines, markers of immune activation, adipokines)
Time Frame
Within 6 months after all patients have completed the study
Title
Establish a diagnosis score based on biomarkers of liver injuries (Adiponectin, leptin, IL6, CRP, CD14)
Description
Quantifiable levels of serum adiponectin, serum leptin, serum HS-IL-6, HS-CRP, serum s-CD14 will be measured.
Time Frame
Within 6 months after all patients have completed the study
Title
Description of pathogenetic factors and correlates with autophagy in liver biopsies of patients with evidence for liver fibrosis
Description
Autophagosome formation in the liver biopsies (only for patients presenting liver fibrosis equal or > 2 will be quantified.
Time Frame
Within 6 months after all patients have completed the study
Title
Identification of features of the adaptive immune system associated to NAFLD, NASH and fibrosis (T cell activation, surface expression of Treg, NK cells, NKT cells)
Description
Quantifiable levels of T cell activation (in PBMC), Frequency and phenotype of Tregs (in PBMC), Quantifiable levels of NK cells (in PBMC), Quantifiable levels of Th17 and γδ T cell (in PBMC), Quantifiable levels of Plasma LPS and LPB (sCD163, CD26, Cytokeratin 18) will be measured.
Time Frame
Within 6 months after all patients have completed the study
Title
Impact of IL28B and PNPLA3 genetic polymorphisms on the severity of liver steatosis, inflammation and fibrosis
Time Frame
Within 6 months after all patients have completed the study
Title
Percentage of patients with NASH, fibrosis and cirrhosis on liver biopsy
Time Frame
Within 6 months after all patients have completed the study
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥40 years
Infection with HIV-1
Cumulative exposure to cART for at least 5 years and currently under cART
Viral load < 400 copies/mL
CD4 count > 100 CD4/mm3
Female may be eligible to enter and participate in the study if she:
is of non-child-bearing potential defined as either post-menopausal (12 months of spontaneous amenorrhea and ≥45 years of age) or physically incapable of becoming pregnant with documented tubal ligation, hysterectomy or bilateral oophorectomy or
is of child-bearing potential with a negative blood pregnancy test at screening visit
Informed consent signed prior to any study procedure
To be covered by a medical insurance (only for French centres)
Presence of:
the metabolic syndrome as defined by the most recent international consensus definition (Alberti et al. Circulation 2009) including three components among the following criteria:
visceral obesity (waist circumference: Europeans and Africans ≥ 94 cm for men and ≥ 80 cm for women, Americans ≥ 102 cm for men and ≥ 88 cm for women, Asians ≥ 90 cm for men and ≥ 80 cm for women)
blood glucose ≥ 1 g/L (5,6 mmol/L) or anti-diabetic treatment,
serum triglycerides ≥ 1,5 g/L (1,7 mmol/L) or hypertriglycerides treatment,
serum HDL cholesterol < 0,4 g/L (1 mmol/L) for men and < 0,5 g/L (1,3 mmol/L) for women or hypercholesterolemia treatment,
blood pressure (Diastolic ≥130 mmHg and/or Systolic ≥ 85 mmHg) or antihypertensive treatment
and/or clinical lipoatrophy and/or lipohypertrophy using clinical questionnaires used and validated in previous published studies (ANRS 121 Hippocampe trial),
and/or chronic elevated transaminases ≥ 1.5 ULN and / or GGT ≥ 2 ULN confirmed by two blood samples within at least three-month interval over twelve months prior screening visit.
Exclusion Criteria:
Coinfection with hepatitis B (positive HBs antigen or isolated positive HBc antibody with positive PCR)
Positive HCV serology
Coinfection HIV-1 and HIV-2
Use of intravenous drugs within the last six months
Excessive alcohol intake (male > 50 g/d, female > 40 g/d)
Other causes of liver diseases i.e: viral hepatitis, hemochromatosis, Wilson disease, autoimmune hepatitis, primary or secondary biliary cirrhosis, primary or secondary cholangitis, α1 antitrypsine deficiency
Other causes of liver steatosis: current steroid therapy, current therapy with amiodarone, tamoxifen, methotrexate, nifedipine, or hycanthone; history of cancer chemotherapy; short bowel syndrome, polycystic ovarian syndrome, Weber-Christian disease
Active opportunistic infection except for candida oesophagitis
Current Cancer
Pregnancy
Decompensated heart failure
Subject under legal guardianship
Inability to give informed consent or incapacitation
Contra-indication to MRI: pace-maker, neurovascular surgery, intraocular materials, cochlear implant, severe claustrophobia
Participation in another study with an ongoing exclusion period at screening
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maud LEMOINE, MD
Organizational Affiliation
Medical Research Council
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Brussels
City
Brussels
Country
Belgium
Facility Name
Hôpital la Salpêtrière
City
Paris
Country
France
Facility Name
Hôpital Saint Antoine
City
Paris
Country
France
Facility Name
Medical Center for Infectious Diseases
City
Berlin
Country
Germany
Facility Name
Center for HIV and Hepato-Gastroenterology
City
Düsseldorf
Country
Germany
Facility Name
University Medical Center
City
Hamburg
Country
Germany
Facility Name
Hannover Medical School
City
Hannover
Country
Germany
12. IPD Sharing Statement
Learn more about this trial
Assessing the Severity of Metabolic-related Liver Injuries in Aging HIV-monoinfected Patients
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