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Consequences of Marijuana Use in HIV-infected Youth

Consequences of Marijuana Use on Inflammatory Pathways in HIV-Infected Youth

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03927053
Enrollment
21
Registered
2019-04-25
Start date
2019-10-31
Completion date
2021-10-15
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Youth With HIV

Keywords

substance use

Brief summary

Proposed study focuses on Youth With HIV (YWH) recruited from the University of North Carolina using a cross sectional assessment of blood samples, clinical, demographic, behavioral, \[including substance use and frequency\], and neurocognitive data will be evaluated from YWH treated before CD4 T cell decline.

Detailed description

The long-term goal for the proposed research is to apply a systems biology approach to discover evidence that provides the basis for understanding the complex and at times conflicting roles for marijuana in chronic inflammation in HIV-infected youth. To achieve the goal, a systems biology approach with two aims is designed: Aim 1. To identify inflammatory immune pathways perturbed by recreational marijuana with or without concomitant use of tobacco products by applying a deep sequencing approach to define global transcriptome of peripheral blood cells from HIV-infected virally suppressed youth. Aim 2. To develop biomarker profiles associated with pro- or anti-inflammatory pathways perturbed by marijuana and to discover biomarker profiles linked to neurocognitive impairment that are impacted by marijuana and tobacco use by YWH

Interventions

None listed

Sponsors

University of North Carolina, Chapel Hill
CollaboratorOTHER
Duke University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 28 Years
Healthy volunteers
No

Inclusion criteria

* Age 21 years 0 days - less than28 years 364 days * Currently treated with stable ART and no ART changes for \>6months. * Willingness to participate in CASI questionnaire of self-reported substance use * Documented behavioral transmission of HIV infection based on CLIA approved HIV antibody/antigen based testing method in medical record -HIV diagnosis greater than or equal to years. Viral load LESS THAN 50 COPIES/ML for the past 6 months. -- Patients may have had single blips in viral load to greater than 50 but less than 1000 copies/ml within the year prior to screening. * Current Substance profile by chart review or phone screening: * Marijuana use defined as marijuana use by any route at least 3 times per week in the absence of tobacco. N= 20. * Tobacco use only based on report of regular (at least 3 times per week smoking). N=24 * Tobacco plus marijuana use defined as regular smoking and marijuana (at least 3 times per week) N =7 * No substance use of any type (alcohol, tobacco, marijuana or other recreational drugs in the past 90 days). N = 10 * Able to provide written informed consent in English and to adhere to protocol schedule

Exclusion criteria

* History of AIDS defining illness * Pregnancy at any time during the study * Use of substances that would interfere with the ability to complete the study * History of significant cognitive or motor impairment or other chronic condition that would interfere with the ability to complete the study and impact neurocognitive testing * Acute psychiatric symptoms (e.g. suicidality, mania, psychosis or severe depression) * Other neurological disorder (e.g. multiple sclerosis, seizure disorder, etc.) requiring ongoing treatment or active outpatient evaluation * Severe mental illness (requiring antipsychotic or mood stabilizing medications and/or inpatient hospitalization in past year) * History of CNS infection (AIDS opportunistic (e.g. toxoplasmosis) or non-opportunistic (bacterial meningitis) with lasting or permanent neurological sequelae) * Underlying and/or uncontrolled medical illnesses that may result in chronic inflammation , (e.g. SLE or autoimmune disease) as determined by the PI * Nursing mothers * Unable to read and write in English

Design outcomes

Primary

MeasureTime frameDescription
Neurocognitive function as measured by WAIS-III (5 subtest IQ estimate)24 months
Number of bio-marker pathways that are abnormal.24 monthsThis is measured by molecular mechanism of chronic macrophage activation.
Plasma levels of sCD16324 monthsChi-square test will be used to compare discrete variables
Neurocognitive function as measured by Trial Making Test (TMT)24 months
Neurocognitive function as measured by Hopkins Verbal Learning Test-R24 months
Neurocognitive function as measured by the Brief Visuospatial Memory Test-R24 months
Neurocognitive function as measured by the WRAT-4 Word Reading subtest24 months
Neurocognitive function as measured by Activities of Daily Living Questionnaire24 months
Neurocognitive function as measured by Behavior Rating Inventory of Executive Functioning24 months
Neurocognitive function as measured by Grooved Pegboard test24 months
Neurocognitive function as measured by Timed Gait Test24 months
Neurocognitive function as measured by Verbal Fluency Test24 Months
Neurocognitive function as measured by Brief Symptom Inventory24 months
Neurocognitive function as measured by Beck Depression Inventory-II24 months
Neurocognitive function as measured by ASSIST (substance abuse)24 months
Neurocognitive function as measured by Base ATN Adherence Questions24 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026