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| ID | Type | Description | Link |
|---|---|---|---|
| 1R01DA044576-01 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
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Despite the advent of safer HIV therapies, high levels of markers of systemic inflammation and increased cardiovascular risk threaten the well-being of individuals living with HIV and present a significant challenge for HIV providers. These risks may be accentuated in HIV-infected individuals who are active intravenous drug users (IVDU); however, this population has been specifically excluded from prior studies assessing immune activation and cardiovascular risk in people living with HIV. In this study, the investigators will specifically target HIV-infected participants who are active IVDU, and co-enroll a control group of HIV-infected participants who never used IV drugs. The investigators will study the specific alterations in immune activation and several mechanisms felt to be potential drivers of immune activation outside of the IVDU population, namely gut integrity alteration, microbial translocation, and oxidized lipids. The investigators will also study the effect of IVDU on markers of arterial inflammation and vascular function. Importantly, the investigators will study the reversibility of immune activation, gut dysfunction, and cardiovascular markers after cessation of IVDU, and to that effect, compare strategies for IVDU cessation-buprenorphine/naloxone versus methadone or vivitrol maintenance treatment.
This is a 48-week matched, prospective, observational, cohort study of HIV-infected adults on antiretroviral therapy who actively use heroin or who have never used heroin. The overarching goals are 1) to define the extent and specifics of immune activation in HIV-infected IV heroin users; 2) to define the effect of IV heroin on gut integrity and permeability, and the relationship of gut integrity alteration and immune activation; 3) importantly, to study the reversibility of immune activation, inflammation, and gut dysfunction after cessation of IV heroin, and to that effect, compare strategies for medication assisted treatment-buprenorphine/naloxone versus methadone or vivitrol maintenance; 4) to study if heightened immune activation associated with active intravenous drug use (IVDU) is associated with higher cardiovascular disease risk, including endothelial dysfunction and arterial inflammation, and if these effects are reversible with buprenorphine/naloxone or methadone.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| HIV-infected adults actively using heroin | HIV-infected adults on antiretroviral therapy who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past. |
| |
| HIV-infected adults never having used heroin | HIV-infected adults on antiretroviral therapy matched to HIV-infected adults actively using heroin by age, sex and CD4+ count. | ||
| HIV-infected adults initiating buprenorphine/naloxone | HIV-infected adults on antiretroviral therapy who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past initiating medication assisted treatment (MAT) for opioid use disorder with buprenorphine/naloxone. |
| |
| HIV-uninfected adults initiating buprenorphine/naloxone | HIV-uninfected adults who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past initiating medication assisted treatment (MAT) for opioid use disorder with buprenorphine/naloxone. |
| |
| HIV-infected adults initiating methadone | HIV-infected adults on antiretroviral therapy who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past initiating medication assisted treatment (MAT) for opioid use disorder with methadone |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| buprenorphine/naloxone | Drug | This is an observational study. Buprenorphine/naloxone for opioid use disorder will be provided in a standardized way by experienced providers through already established funded treatment programs. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in plasma soluble CD14 concentration | soluble marker of monocyte activation | 48 weeks |
| Change in Endopat measure of microvascular function | Measure of endothelial function | 48 weeks |
| Change in target to background ratio measured by fluorodeoxyglucose (FDG)-positron emission tomography (PET) | Measure of vascular inflammation | 48 weeks |
| Change in plasma Interferon Gamma-Induced Protein 10 concentration | soluble marker of inflammation | 48 weeks |
| Change in plasma intestinal fatty acid binding protein concentration | soluble marker of gut integrity | 48 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in total fat stores measured by Whole body Dual-energy X-ray absorptiometry | Measurement of fat stores | 48 weeks |
| Change in aortofemoral pulse wave velocity | Measure of arterial stiffness |
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Inclusion Criteria:
Exclusion Criteria:
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Adults ages 18 to 80 years with and without HIV infection using heroin or initiating treatment for heroin use or not using heroin.
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| Name | Affiliation | Role |
|---|---|---|
| Corrilynn O Hileman, MD | MetroHealth Medical Center | Principal Investigator |
| Grace A McComsey, MD | University Hospitals Cleveland Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospitals Cleveland Medical Center | Cleveland | Ohio | 44106 | United States | ||
| Metrohealth Medical center |
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| ID | Term |
|---|---|
| D015658 | HIV Infections |
| D009293 | Opioid-Related Disorders |
| D002318 | Cardiovascular Diseases |
| D007249 | Inflammation |
| ID | Term |
|---|---|
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
| D015229 | Sexually Transmitted Diseases, Viral |
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| ID | Term |
|---|---|
| D000069479 | Buprenorphine, Naloxone Drug Combination |
| D008691 | Methadone |
| D009271 | Naltrexone |
| C000624616 | vivitrol |
| D003932 | Heroin |
| ID | Term |
|---|---|
| D002047 | Buprenorphine |
| D009019 | Morphinans |
| D053610 | Opiate Alkaloids |
| D000470 | Alkaloids |
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Plasma, serum, urine, stool, peripheral blood mononuclear cells
|
| HIV-infected adults initiating Vivitrol | HIV-infected adults on antiretroviral therapy who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past initiating medication assisted treatment (MAT) for opioid use disorder with Vivitrol. |
|
| HIV-uninfected adults initiating methadone | HIV-uninfected adults who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past initiating medication assisted treatment (MAT) for opioid use disorder with methadone. |
|
| HIV-uninfected adults initiating Vivitrol | HIV-uninfected adults who are currently using heroin at least 1 month with a cumulative duration of at least 12 months in the past initiating medication assisted treatment (MAT) for opioid use disorder with Vivitrol. |
|
| Methadone | Drug | This is an observational study. Methadone for opioid use disorder will be provided in a standardized way by experienced providers through already established funded treatment programs. |
|
| Naltrexone Injection | Drug | This is an observational study. Naltrexone injection for opioid use disorder will be provided in a standardized way by experienced providers through already established funded treatment programs. |
|
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| Heroin | Drug | This is an observational study. Participants using heroin will be enrolled into this group. |
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| 48 weeks |
| Change is waist to hip ratio | Measurement of central obesity | 48 weeks |
| Change in body mass index | Body measurement | 48 weeks |
| Cleveland |
| Ohio |
| 44109 |
| United States |
| D012749 | Sexually Transmitted Diseases |
| D016180 | Lentivirus Infections |
| D012192 | Retroviridae Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D000079524 | Narcotic-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006571 |
| Heterocyclic Compounds |
| D009270 | Naloxone |
| D006572 | Heterocyclic Compounds, Bridged-Ring |
| D006576 | Heterocyclic Compounds, 4 or More Rings |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D010616 | Phenanthrenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D011083 | Polycyclic Compounds |
| D004338 | Drug Combinations |
| D004364 | Pharmaceutical Preparations |
| D007659 | Ketones |
| D009930 | Organic Chemicals |
| D009022 | Morphine Derivatives |