Depression, HIV-Associated Cognitive Motor Complex, HIV Infections
Conditions
Keywords
11C-DASB, 18F-Fluoro-L-dopa, HIV, Depression, Positron Emission Tomography (PET)
Brief summary
Background: Human immunodeficiency virus (HIV) infection is a serious disease with no cure. Some people with HIV have depression and other mood problems. They can have problems with thinking and memory. Researchers think 2 chemicals in the brain may cause those problems. The chemicals are serotonin and dopamine. The researchers want to take images to learn more about those chemicals in HIV patients. Objective: To learn how HIV affects serotonin and dopamine in the brain. Eligibility: Adults ages 18-70 with HIV who have been on antiretroviral treatment for at least 1 year Healthy adults ages 18-70 All participants must be already enrolled in protocol 13-N-0149. Design: * Participants will be screened with a urine drug test. The results could be shared with insurance companies. * Participants who could be pregnant will have a pregnancy test. * Participants may have a physical exam and blood tests. * Participants will have 1 or 2 positron emission tomography (PET) scans. A needle will guide a thin plastic tube (catheter) into an arm vein. A radioactive drug will be injected into the plastic tube. This is a tracer that helps researchers understand the PET images. * Participants who have the dopamine scan will have to fast for 4-6 hours before the scan. They will take a pill to help direct the tracer to the brain one hour before the scan. * Each scan will last about 1.5 hours. * Participants will be asked to drink a lot of fluids and empty their bladder frequently for the rest of the day after each scan.
Detailed description
Background: An extensive body of literature points towards neuronal brain injury in human immunodeficiency virus positive (HIV-positive) subjects despite virological suppression of the virus in the periphery under the effect of antiretroviral therapies (ART). Existing evidence suggests that the central nervous system (CNS) could be an important reservoir for human immunodeficiency virus (HIV) regardless of cumulative time on treatment. This results in progressive neurocognitive dysfunction despite optimal treatment and peripheral control of the infection. Even though structural imaging studies have described abnormalities in optimally-treated HIV-positive subject population, there has been only a few attempts at deciphering the cellular levels of brain damage in those subjects using in vivo molecular imaging biomarkers. As part of CNS involvement, specific neurotransmitter systems including the dopaminergic and serotonergic systems are thought to be affected by the infection with distinct neurological, cognitive and psychological manifestations, even in optimally-treated subjects. Objective: This protocol aims at identifying aspects of dopaminergic and serotonergic dysfunction in optimally-treated HIV-positive subjects using high resolution positron emission tomography (PET) of the brain and radioligands targeted against the dopaminergic (18F-FDOPA) and serotonergic (11C-DASB) systems. Study population: We will identify 25 eligible HIV-infected individuals and 50 eligible HIV-negative (HIV-) individuals for the dopaminergic arm, and 20 HIV-infected individuals and 20 HIV-negative individuals for the serotonergic arm. Subjects will be selected from IRB approved NIH protocols, self-referred or will be referred form outside providers/institutions and those who meet eligibility criteria will be offered enrollment in our study. Design: Subjects will undergo either a one-time 18F-FDOPA PET scan or a one-time 11C-DASB PET scan or both, if eligible. HIV-positive subjects and HIV-negative individuals will be included in the study. Outcome Measures: Influx constant (Ki) for 18F-FDOPA PET and Binding potential relative to non-displaceable binding (BPND) values for 11C-DASB PET
Interventions
Sponsors
National Institutes of Health Clinical Center (CC)
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* INCLUSION CRITERIA: Subject groups: * Dopaminergic arm: * Group A: HIV-positive subjects with or without co-morbidities * Group B: HIV-negative subjects with co-morbidities * Group C: HIV-negative subjects without co-morbidities * Serotonergic arm: * Group D: HIV-positive subjects with or without co-morbidities * Group E: HIV-negative subjects with or without co-morbidities All Subjects (Groups A-E): 1. Men and women, 18-70 years of age 2. Ability to sign informed consent by the subject 3. Subjects may be enrolled in or have been discharged from IRB approved NIH protocols OR subjects may be referred from outside providers/institutions. 4. Has the ability to be seen by an outside medical doctor who provides care. All HIV-positive Subjects with or without co- morbidities (Groups A \[dopaminergic arm, n=25)\] and Group D \[serotonergic arm, n=20\]) 1. Known and documented HIV-1 infection 2. Plasma HIV-RNA BLD (\<100 copies/mm3) for greater than one year since the last available documented viral load measurement.. 3. At least one year of continuous ART prior to last documented suppressed viral load measurement and no history of ART modification or interruption since then. HIV-negative Subjects WITH Co-morbidities (Group B, n=25) 1. HIV-antibody negative 2. At least one or more of the following criteria: 1. Hypertension, as defined by treatment with medications for hypertension or with a systolic blood pressure at screening greater than or equal to 140mm Hg. 2. Diabetes mellitus, as defined by HgbA1C greater than or equal to 6.5% or known treatment for diabetes. 3. Hepatitis C infection as documented by lab results of a positive Hepatitis C antibody and/or detectable Hepatitis C viral load. Subjects who responded to HCV treatment (SVR) will be included. 4. History of previous but not current drug abuse. 5. History of previous but not current alcoholism (defined as alcohol intake that affect/affected the subject s work or home life). 6. Clinical atherosclerotic cardiovascular disease (ASCVD) (e.g. history of acute coronary syndromes, or myocardial infarction, stable or unstable angina, coronary or other arterial revascularization or peripheral arterial disease of atherosclerotic origin) and/or 10-year heart disease risk score (ASCVD risk score) \>7.5% (7.5 % score is the threshold for starting statin therapy as per the 2013 American College of Cardiology \[ACC\] / American Heart Association \[AHA\] guidelines). HIV-negative Subjects WITHOUT co-morbidities (Group C, n=25) 1. HIV-antibody negative 2. No history of any of the following: 1. Hypertension, as defined by treatment with medications for hypertension or with a systolic blood pressure at screening greater than or equal to 140mm Hg. 2. Diabetes mellitus, as defined HgbA1C greater than or equal to 6.5% or treatment for diabetes. 3. Hepatitis C infection as documented by lab results of positive Hepatitis C antibody and/or detectable Hepatitis C viral load. Subjects who responded to HCV treatment (SVR) will not be included. 4. History of previous drug abuse. 5. History of previous alcoholism. Alcoholism is based on alcohol having affected the subject s work or home life. 6. Clinical ASCVD (e.g. history of acute coronary syndromes, or myocardial infarction, stable or unstable angina, coronary or other arterial revascularization or peripheral arterial disease of atherosclerotic origin) and/or 10-year heart disease risk score (ASCVD risk score) \>7.5% (7.5 % score is the threshold for starting statin therapy as per the 2013 ACC/AHA guidelines 35). 7. Any other disease entities including chronic infections (e.g. Hepatitis B, Lyme disease), neurological diseases (e.g. Multiple sclerosis, vasculitis) or systemic diseases (e.g. Sjogren s diseases, sarcoidosis, systemic lupus erythematosus \[SLE\]) that in the opinion of the investigator would be considered a significant co-morbidity. HIV-negative Subjects with or without co- morbidities (Group E, n=20) 1\. HIV-antibody negative
Exclusion criteria
All Subjects (Groups A-E): 1. Illness or other condition that, in the opinion of the PI, may interfere with study participation at the time of enrollment, including known history of significant intracranial structural damage such as previous stroke(s) or history of intracranial benign or malignant tumors. 2. Conditions other than HAND associated with cognitive impairment or dementia such as Alzheimer s, Parkinson s disease, head injury with loss of consciousness \>30 minutes, or seizure disorders. 3. A positive screening result for psychiatric diseases that are known to affect the dopaminergic or serotonergic systems. 4. Current substance abuse that would interfere with PET scan results at the investigators discretion. 5. Medications: use of any drug with known dopaminergic or serotonergic activity within 6 months prior to planned imaging date(s). 6. Pregnant or Lactating women: Women of childbearing potential must have a negative serum or urine pregnancy test within 1 week prior to study entry. Pregnancy testing will also be performed in enrolled female participants prior to any radiation exposure. 7. Prior or planned/anticipated exposure to radiation due to clinical care or participation in other research protocols, which would exceed the recommended acceptable annual limit of radiation exposure once accounting for the requirements of the current study. Additional
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Influx Constant (Ki) for 18F-FDOPA PET. | 90 minutes of scanning | in order to learn how HIV affects dopamine in the brain, we performed dynamic PET scans for 90 minutes in each patient, after injection of FDOPA. Analysis: After the scans were reconstructed, we extracted the Time activity curves and performed compartmental analysis using Patlak linear graphical analysis with reference region. The extracted outcome measure is the influx constant referred to as Ki and reflecting the rate of FDOPA uptake in specific brain regions. |
| 11C-DASB PET Binding Potential | 90 minutes of scanning | Binding potential is a measure of the density of available serotonin transporter in specific brain locations. This is extracted from time activity curves of dynamic PET data acquired over 90 minutes after injection of 11C-DASB. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Correlation of 18F-FDOPA With Co-morbidities | Study and statistical analysis Completion | Correlation of 18F-FDOPA uptake in the brain with co-morbidities such as cardiovascular disease |
| Correlation of 18F-FDOPA and 11C-DASB With HIV | Study and statistical analysis Completion | Correlation of 18F-FDOPA and 11C-DASB with HIV infection parameters (e.g. time since HIV diagnosis, duration of infection before treatment initiation, nadir CD4). |
| Correlation of 11C-DASB With Neuropsychiatric Evaluation | Study and statistical analysis Completion | Correlation of 11C-DASB with Neuropsychiatric evaluation (e.g. depressive and executive function/cognitive scores). |
Countries
United States
Participant flow
Recruitment details
Subjects were recruited through protocol number 13-N-0149, other IRB- approved intramural NIH protocols, or through referrals from outside providers/ institutions or self-referred. Once consented and found eligible, subjects underwent PET scanning using 18FDOPA and / or 11C-DASB. All visits were on a outpatient basis. There were not follow-up visits after the completion of the PET scan(s) The recruitment and enrollment process for this study occurred from 11/20/2018 through 11/5/2021
Pre-assignment details
Among HIV positive subjects: 1 subject didn't show up to either scan 2 subjects couldn't finish FDOPA and didn't come back for DASB 2 subjects did FDOPA but didn't come back for DASB Among HIV negative subjects 1 subject did DASB but didn't come back for FDOPA
Participants by arm
| Arm | Count |
|---|---|
| HIV Positive Participants (Dopaminergic and Serotonergic Studies) 25 eligible HIV-infected individuals for the dopaminergic arm
18F-FDOPA: High resolution positron emission tomography (PET) of the brain and radioligands targeted against the dopaminergic (18F-FDOPA) system.
20 eligible HIV-infected individuals for the serotonergic arm
11C-DASB: High resolution positron emission tomography (PET) of the brain and radioligands targeted against the serotonergic (11C-DASB) system. | 23 |
| HIV Negative Participants (Dopaminergic and Serotonergic Studies) 50 eligible HIV-negative (HIV-) individuals for the dopaminergic arm
18F-FDOPA: High resolution positron emission tomography (PET) of the brain and radioligands targeted against the dopaminergic (18F-FDOPA) system.
20 eligible HIV-negative individuals for the serotonergic arm
11C-DASB: High resolution positron emission tomography (PET) of the brain and radioligands targeted against the serotonergic (11C-DASB) system. | 23 |
| Total | 46 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Dopaminergic Study | could not finish FDOPA scan | 2 | 0 |
| Dopaminergic Study | Withdrawal by Subject | 1 | 1 |
| Serotonergic Study | Withdrawal by Subject | 5 | 1 |
Baseline characteristics
| Characteristic | HIV Positive Participants (Dopaminergic and Serotonergic Studies) | HIV Negative Participants (Dopaminergic and Serotonergic Studies) | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 2 Participants | 2 Participants | 4 Participants |
| Age, Categorical Between 18 and 65 years | 18 Participants | 21 Participants | 39 Participants |
| participant numbers | 20 Participants | 23 Participants | 43 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 9 Participants | 13 Participants | 22 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 11 Participants | 10 Participants | 21 Participants |
| Sex: Female, Male Female | 6 Participants | 9 Participants | 15 Participants |
| Sex: Female, Male Male | 14 Participants | 14 Participants | 28 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 23 | 0 / 23 |
| other Total, other adverse events | 0 / 23 | 0 / 23 |
| serious Total, serious adverse events | 0 / 23 | 0 / 23 |
Outcome results
Primary
11C-DASB PET Binding Potential
Binding potential is a measure of the density of available serotonin transporter in specific brain locations. This is extracted from time activity curves of dynamic PET data acquired over 90 minutes after injection of 11C-DASB.
Time frame: 90 minutes of scanning
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Dopaminergic Arm Group A | 11C-DASB PET Binding Potential | 2.949 unitless | Standard Deviation 0.395 |
| Dopaminergic Arm Group B/C | 11C-DASB PET Binding Potential | 3.256 unitless | Standard Deviation 0.597 |
Primary
Influx Constant (Ki) for 18F-FDOPA PET.
in order to learn how HIV affects dopamine in the brain, we performed dynamic PET scans for 90 minutes in each patient, after injection of FDOPA. Analysis: After the scans were reconstructed, we extracted the Time activity curves and performed compartmental analysis using Patlak linear graphical analysis with reference region. The extracted outcome measure is the influx constant referred to as Ki and reflecting the rate of FDOPA uptake in specific brain regions.
Time frame: 90 minutes of scanning
Population: All participants who completed FDOPA PET scan with usable Data
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Dopaminergic Arm Group A | Influx Constant (Ki) for 18F-FDOPA PET. | Caudate | 0.01415 min-1 | Standard Deviation 0.00136 |
| Dopaminergic Arm Group A | Influx Constant (Ki) for 18F-FDOPA PET. | Putamen | 0.01588 min-1 | Standard Deviation 0.00127 |
| Dopaminergic Arm Group B/C | Influx Constant (Ki) for 18F-FDOPA PET. | Caudate | 0.01409 min-1 | Standard Deviation 0.00126 |
| Dopaminergic Arm Group B/C | Influx Constant (Ki) for 18F-FDOPA PET. | Putamen | 0.01592 min-1 | Standard Deviation 0.00127 |
Secondary
Correlation of 11C-DASB With Neuropsychiatric Evaluation
Correlation of 11C-DASB with Neuropsychiatric evaluation (e.g. depressive and executive function/cognitive scores).
Time frame: Study and statistical analysis Completion
Secondary
Correlation of 18F-FDOPA and 11C-DASB With HIV
Correlation of 18F-FDOPA and 11C-DASB with HIV infection parameters (e.g. time since HIV diagnosis, duration of infection before treatment initiation, nadir CD4).
Time frame: Study and statistical analysis Completion
Secondary
Correlation of 18F-FDOPA With Co-morbidities
Correlation of 18F-FDOPA uptake in the brain with co-morbidities such as cardiovascular disease
Time frame: Study and statistical analysis Completion