HIV-1-infection, Antiviral Drug Adverse Reaction, Vascular Diseases, Cardiovascular Abnormalities, Abnormality of Adipose Tissue, Body Weight Changes, Body Fat Disorder, HIV-Associated Lipodystrophy Syndrome
Conditions
Brief summary
The goal of the study is to combine a collaborative and translational approach to evaluate the effect antiretroviral regimen switch to a dolutegravir containing regimen compared to continued treatment with a non- dolutegravir based regimen on on lipid and metabolic profiles, renal function, body composition, vascular function and diet.
Detailed description
Over the last decades, the use of combined antiretroviral therapy has led to profound suppression of HIV-1 replication and increased the survival of persons living with HIV (PLWH) to close to that of the general population. As a consequence, the spectrum of diseases related to HIV has shifted from opportunistic AIDS-related diseases towards long-term-age-related complications. Individuals living with HIV are now exhibiting accelerated development of obesity, metabolic derangements and cardiovascular disease (CVD). Recent compelling clinical evidence has documented a drastic shift in anthropometric profiles among persons living with HIV. In addition, several reports present dolutegravir, a second-generation integrase inhibitor currently highly prescribed for its high antiviral efficiency, as the potential cause of unpredicted weight gain. A critical gap in the investigators' knowledge is a lack of understanding of the etiopathology of the contribution of dolutegravir on weight gain and the consequential impact on obesity and cardiovascular disease in persons living with HIV on combined antiretroviral therapy. As overweight and obesity are among the leading risk factors for cardiovascular disease in persons living with HIV, it is critical to directly investigate whether dolutegravir increases fat mass in persons living with HIV and whether body weight gains-associated with dolutegravir based regimen contribute to the increased prevalence of CVD in this population of people. This application seeks to investigate alterations in body fat and cardiometabolic risk markers associated with dolutegravir. The investigators propose that in patients with undetectable plasma HIV RNA, there is a direct correlation of weight gain and dolutegravir after antiretroviral regimen switch. They also contend that dolutegravir associated weight gain induces a phenotypic metabolic shift which alters the vascular endothelium and potentiates CVD risk. If the investigators are correct in their hypotheses, modifications in the clinical practice of treatment and prevention strategies for CVD in people living with HIV may be warranted. Herein the investigators propose a novel translational study which will concomitantly investigate in human patients and animal models of HIV: 1. whether dolutegravir based regimen increases body weight 2. the mechanisms whereby dolutegravir increases body weight 3. whether dolutegravir-mediated body weight gain increases the risk for CVD in PLWH.
Interventions
15 participants will be randomized to remain on fully suppressive background antiretroviral therapy. The third agent will be switched to dolutegravir at the dose of 50 mg daily.
15 participants with suppressed HIV disease for greater than or equal to 3 months will be randomized to remain on their current 2 or 3 drug fully suppressive antiretroviral regimen.
Sponsors
Study design
Intervention model description
The study design is a randomized control trial where patients will be randomized to the dolutegravir or non-dolutegravir arms by random number generation using the statistical software R. A unique identification (ID) key from 1 to 2n will be assigned to each patient. Additionally, the investigators will utilize a parallel mouse model of HIV mimicking PLWH with stable viral load that can provide mechanistic insight and integrate experiments at the tissue level (adipose tissue) as well. Experiments in the parallel mouse model of HIV will also present the advantage to enable the study the direct effects of HIV viral infection on metabolic and cardiovascular function, a study not feasible in PWH who, for easily understandable ethical reasons, cannot remain without treatment for 6 months (duration of the study).
Eligibility
Inclusion criteria
Subjects must meet the following criteria to be eligible for participation in this study: * Age greater than or equal to 18 years with HIV-1 who have been virologically suppressed (HIV-1 RNA \< 50 copies for greater than or equal to 3 months on a non-integrase strand transfer inhibitor-based regimen * Have the ability to understand and sign an informed consent written in the English language
Exclusion criteria
Subjects meeting any of the following
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Weight | 24 weeks | Change from baseline kilograms (kg) of weight at 24 weeks |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in body mass index (BMI) | 24 weeks | Total change in body mass index -height and weight will be combined to report BMI (Kilogram/Height in centimeters\^2) |
| Change in vascular endothelial function | 24 weeks | Change from baseline vessel diameter (millimeters) at 24 weeks |
| Height | 24 weeks | Measurement of height (centimeters) from baseline to 24 weeks |
Other
| Measure | Time frame | Description |
|---|---|---|
| Change in low density lipoprotein (LDL) | 24 weeks | Change from baseline LDL (mg/dL) at 24 weeks |
| Change in quantity of food consumption | 24 weeks | Change from baseline of calorie consumption (kcal) at 24 weeks |
| Change in fasting serum glucose level | 24 weeks | Change from baseline serum glucose level (mg/dL) at 24 weeks |
| Change in HIV-1 RNA viral load | 24 weeks | Change from baseline HIV-1 viral load (copies) at 24 weeks |
| Change in cholesterol | 24 weeks | Change from baseline cholesterol (mg/dL) at 24 weeks |
| Change in triglycerides | 24 weeks | Change from baseline triglycerides (mg/dL) at 24 weeks |
| Change in high density lipoprotein (HDL) | 24 weeks | Change from baseline HDL (mg/dL) at 24 weeks |
Countries
United States