Comparison of Inflammatory Markers and Incidence of Comorbidities in Patients on Antiretroviral Therapy With Second-generation Anti-integrase Drugs on Triple Versus Dual Therapy
- Conditions
- Hiv
- Interventions
- Other: plasma inflammatory markersOther: CD4/CD8 ratio
- Registration Number
- NCT05699785
- Lead Sponsor
- Centre Hospitalier Universitaire de Nice
- Brief Summary
HIV-infected patients develop comorbidities earlier than the general population. Immune activation with the secretion of pro-inflammatory cytokines would play a major role in the occurrence of these comorbidities. Numerous factors, called risk factors, already identified in the general population and confirmed in patients with HIV virus favor the occurrence of these comorbidities but cannot alone explain the overrepresentation and precocity of these comorbidities in the HIV population. Investigators hypothesize that optimization or simplification with certain classes of antiretrovirals modify the inflammatory response and are predictive factors for the occurrence of comorbidities
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 500
- HIV-1 infection
- Age > 40 years or adults with more than 10 years of antiretroviral therapy
- Switching to BIC/FTC/TAF or DTG/3TC or DTG+3TC within the last 2 years
- Plasma HIV-1 RNA viral load < 50 copies/ml for more than 6 months
- Absence of chronic hepatitis B infection
- Absence of genotype mutations on Dolutegravir (DTG) or Bictegravir (BIC) or tenofovir alafenamide TAF
- Daily use of antiretroviral therapy
- Effective contraception for women of childbearing potential will be requested
- Signed informed consent
- Enrollment in a Social Security plan
- Non-daily or intermittent antiretroviral therapy regimen (e.g., 4 or 5 days a week)
- Pregnancy or breastfeeding
- Vulnerable persons according to article L.1121-6 of the public health code Persons unable to give consent according to article L.1121-8 of the public health code
- Opportunistic infections during curative treatment
- HIV-2 infection
- Active hepatitis C
- Refusal to participate
- Withdrawal of informed consent by the patient
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description patients on antiretroviral therapy with second generation anti-integrase drugs in dual therapy CD4/CD8 ratio - patients on antiretroviral therapy with second generation anti-integrase drugs in triple therapy CD4/CD8 ratio - patients on antiretroviral therapy with second generation anti-integrase drugs in triple therapy plasma inflammatory markers - patients on antiretroviral therapy with second generation anti-integrase drugs in dual therapy plasma inflammatory markers -
- Primary Outcome Measures
Name Time Method Plasma inflammatory markers 3 years after baseline To measure the evolution of different plasma inflammatory markers (CRP, IL6, D-Dimers, CD14s, CD163, IL-1, IP-10, MCP-1, IL-18, IFAB) over 3 years between the 2 groups.
CD4/CD8 ratio 3 years after baseline To measure the evolution of CD4/CD8 ratio over 3 years between the 2 groups. A CD4/CD8 ratio is considered normal if it is greater than 0.75. Immune hyperactivation occurs when the ratio is below 0.75
- Secondary Outcome Measures
Name Time Method Virological failure rate (year 1) One year after baseline Virological failure rate (plasma HIV-1 RNA viral load \> 50 copies/ml on two consecutive measurements)
residual viremia rate (year 1) One year after baseline Evolution of the residual viremia rate (detected or quantifiable plasma HIV-1 RNA viral load \< 50 copies/ml)
plasma markers assay (year 1) 1 year after baseline Analyze the evolution of plasma markers at 1 year between the two cohorts in high-risk subjects (nadir CD4\<200 cells/mm3 or history of AIDS stage, or subject aged ≥ 65 years)
plasma markers assay (year 2) 2 years after baseline Analyze the evolution of plasma markers at 2 years between the two cohorts in high-risk subjects (nadir CD4\<200 cells/mm3 or history of AIDS stage, or subject aged ≥ 65 years)
plasma markers assay (year 3) 3 years after baseline Analyze the evolution of plasma markers at 3 years between the two cohorts in high-risk subjects (nadir CD4\<200 cells/mm3 or history of AIDS stage, or subject aged ≥ 65 years)
comorbidities (year 2) 2 years after baseline Measurement of the true incidence of major 11 comorbidities (Depression, Cardiovascular, Osteoporosis, Non-AIDS related cancers, Metabolic syndrome, Cognitive disorders, Chronic renal failure , proximal renal tubulopathy, Hepatic fibrosis, Chronic Obstructive Pulmonary Disease, Osteoarthritis) at 2 years
patient profiles 3 years after baseline Describe patient profiles at risk for comorbidities based on different inflammatory biomarkers
Virological failure rate (year 3) three years after baseline Virological failure rate (plasma HIV-1 RNA viral load \> 50 copies/ml on two consecutive measurements)
risk factors for immune hyper activation 3 years after baseline Analyze and compare risk factors for immune hyper activation (age, CD4 nadir\<200 cells/mm3, AIDS stage, residual viremia, archived M184V/I resistance...) in each group
comorbidities (year 1) 1 year after baseline Measurement of the true incidence of major 11 comorbidities (Depression, Cardiovascular, Osteoporosis, Non-AIDS related cancers, Metabolic syndrome, Cognitive disorders, Chronic renal failure , proximal renal tubulopathy, Hepatic fibrosis, Chronic Obstructive Pulmonary Disease, Osteoarthritis) at 1 year
individualized and computerized care plan 3 years after baseline Establish an individualized and computerized care plan for the patient after evaluation of the risk factors (according to the profiles) to detect the occurrence or aggravation of comorbidities
Prevalence of neuropsychiatric events at 3 years 3 years after baseline To analyze the evolution at 2 years of the prevalence of neuropsychiatric events (including sleep disorders, anxiety, depression) between the two groups from the questionnaires.
changes in antiretroviral therapy (year 2) 2 years after baseline Analyze the 2-years change in the prevalence of changes in antiretroviral therapy and the reasons for changes between the two groups based on questionnaires
Onset of new comorbidity 3 years after baseline Measure the time to onset of new comorbidity(ies) in each group.
Virological failure rate (year 2) two years after baseline Virological failure rate (plasma HIV-1 RNA viral load \> 50 copies/ml on two consecutive measurements)
Residual viremia rate (year 2) two years after baseline Evolution of the residual viremia rate (detected or quantifiable plasma HIV-1 RNA viral load \< 50 copies/ml)
Prevalence of neuropsychiatric events at 1 year 1 year after baseline To analyze the evolution at 1 year of the prevalence of neuropsychiatric events (including sleep disorders, anxiety, depression) between the two groups from the questionnaires.
changes in antiretroviral therapy (year 1) 1 year after baseline Analyze the 1-year change in the prevalence of changes in antiretroviral therapy and the reasons for changes between the two groups based on questionnaires
Evolution of intracellular markers (CD8/CD38, HLA-DR) (year 1) 1 year after baseline To analyze the evolution of intracellular markers (CD8/CD38, HLA-DR) at 1 year between the two cohorts in high-risk subjects (nadir CD4\<200 cells/mm3 or history of AIDS stage, or subject aged ≥ 65 years)
immune activation markers assays and identification of comorbidities 3 years after baseline Correlate immune activation markers with the occurrence of comorbidities
comorbidities (year 3) 3 years after baseline Measurement of the true incidence of major 11 comorbidities (Depression, Cardiovascular, Osteoporosis, Non-AIDS related cancers, Metabolic syndrome, Cognitive disorders, Chronic renal failure , proximal renal tubulopathy, Hepatic fibrosis, Chronic Obstructive Pulmonary Disease, Osteoarthritis) at 3 years
Residuak viremia rate (year 3) 3 years after baseline Evolution of the residual viremia rate (detected or quantifiable plasma HIV-1 RNA viral load \< 50 copies/ml)
Prevalence of neuropsychiatric events at 2 years 2 years after baseline To analyze the evolution at 2 years of the prevalence of neuropsychiatric events (including sleep disorders, anxiety, depression) between the two groups from the questionnaires.
changes in antiretroviral therapy (year 3) 3 years after baseline Analyze the 3-years change in the prevalence of changes in antiretroviral therapy and the reasons for changes between the two groups based on questionnaires
Trial Locations
- Locations (2)
CH Simone VEIL
🇫🇷Cannes, France
CHU Nice
🇫🇷Nice, France