Investigating the Mu:Kappa Opioid Receptor Imbalance in Alcohol Use Disorder
- Conditions
- Alcohol Use Disorder
- Interventions
- Radiation: PKABOther: Detoxification ProgramRadiation: CFN
- Registration Number
- NCT05957159
- Lead Sponsor
- Yale University
- Brief Summary
The primary objective of this multimodal positron emission tomography (PET) study is to use PET brain imaging to measure both MOR (Mu-Opioid receptors) and KOR (kappa-opioid receptors) in participants with alcohol use disorder (AUD) and to quantify the relationships between MOR and KOR, separately and jointly, to key clinical outcomes (e.g., craving, mood, withdrawal, time to lapse) during a quit attempt.
- Detailed Description
Primary Objective
The primary objective of this multimodal positron emission tomography (PET) study is to use PET brain imaging to measure both MOR (Mu-Opioid receptors) and KOR (kappa-opioid receptors) in participants with alcohol use disorder (AUD) and to quantify the relationships between MOR and KOR, separately and jointly, to key clinical outcomes (e.g., craving, mood, withdrawal, time to lapse) during a quit attempt. Investigators will achieve this goal by completing the following aims:
Aim 1: To determine whether participants with AUD in early abstinence (up to 6 days) have altered MOR and KOR availability compared to healthy subjects. Investigators propose to recruit 50 people with AUD (DSM-5 diagnosis) and 50 age- and sex-matched controls to each participate in one \[11C\]CFN and one \[11C\]PKAB PET scan. Participants with AUD will participate either 1) in a medically supervised inpatient unit, the Clinical Neuroscience Research Unit (CNRU), for \~6 days, or 2) will stop drinking on an outpatient basis with daily meetings for \~6 days. Measures of craving (including a cue reactivity task), mood, withdrawal, and drinking outcomes will be collected. Hypothesis: participants with AUD will have significantly higher MOR in ventral striatum, but lower KOR in amygdala and whole striatum compared to control participants.
Aim 2: To relate measures of MOR and KOR availability to clinical outcomes during early and late abstinence. Early abstinence (\~6 days) will be followed by an outpatient quit attempt for an additional 3 weeks supported by contingency management. Measures of craving, mood, withdrawal, and drinking outcomes will be collected throughout the study. Hypothesis: Taken one at a time, MOR availability in ventral striatum as well as KOR in the amygdala and whole striatum will each be significantly associated with abstinence-induced craving, mood, withdrawal, and time to lapse in participants with AUD.
Aim 3: To maximize use of neuroimaging data via machine-learning-based clustering to identify biomarkers of the joint (MOR, KOR) dataset that characterize clinical outcomes in AUD during a quit attempt. Primary. The investigators will determine whether clusters of AUD patients based on features of the joint (MOR, KOR) data are significantly associated with distinct clinical outcomes (e.g., time to lapse) during a quit attempt. Secondary. Investigators will test the classification accuracy of our clustering approach. Hypotheses: Clustering of joint (MOR, KOR) data will yield clusters of AUD patients with significantly different clinical responses to a quit attempt. Clusters will be more compact (distinct) than if based on demographics or a single type of PET image, alone. A classification scheme based on (MOR, KOR) data will assign individual patients to pre-defined clusters with high classification accuracy, that is, to the cluster that best reflects their clinical outcomes.
Aim 4: To determine whether MOR and KOR availability normalizes over the course of abstinence. Subjects who do not drop out of the study in the first 3 weeks may return for one \[11C\]CFN, one \[11C\]PKAB PET scan, and one MRI during weeks 3-6 of the study. This will allow us to gain information on the changes in the MOR and KOR systems that occur during a quit attempt. Investigators hypothesize a reduction in MOR and increase in KOR within subject in participants who are able to maintain abstinence.
Secondary Objective (if applicable) The secondary objective of this study is to evaluate the predictive ability of the clustering method, i.e., its potential for personalized prediction of individual clinical outcomes. For any 'new' subject not used for the initial clustering, investigators will assign it to a cluster by a K-nearest neighbor approach.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 100
- Participants with AUD will have a current diagnosis of AUD according to DSM-5 criteria (i.e., SCID-5 ascertained diagnosis, confirmed by the Principal Investigators);
- Participants with AUD will meet the following drinking criteria: males will drink > 14 drinks per week and exceed 4 drinks per day at least twice per week; females will drink > 7 drinks per week and exceed 3 drinks per day at least twice per week. They must meet drinking criteria during a consecutive 30-day period within the 90 days prior to intake;
- Participants with AUD will indicate willingness to abstain from alcohol and engage in a quit attempt;
- Healthy subjects will have no current or past diagnosis of AUD or other significant substance use disorder. They will drink less than 5 alcoholic drinks per week with no heavy drinking days (i.e., >4 drinks/day for men; >3 drinks/day for women) in the last 30 days;
- Able to read and write English and to provide voluntary, written informed consent;
- Agree to have blood drawn for genotyping of the OPRM1 which has been shown to impact the [11C]CFN outcome measure, BPND50.
- Current significant medical condition such as neurological, cardiovascular, endocrine, renal, liver, or thyroid pathology that would impact the integrity of the data (note that elevated liver enzymes for individuals with AUD will not be exclusionary);
- Past or current neurological disorder or disorders affecting the brain including but not limited to multiple sclerosis, history of stroke, brain tumors, traumatic brain injury with loss of consciousness, seizure disorder;
- Current significant psychiatric disorder including severe substance use disorder (other than alcohol or tobacco use disorders*), and past or current psychotic symptoms;
- Regular use in the past 6 months of any prescription, psychoactive or herbal medications (e.g., antidepressants, antipsychotics, anxiolytics) that would impact the integrity of the data (e.g., naltrexone); No subject will be asked to stop taking medication to participate in the study;
- Women who are pregnant or nursing, or fail to use one of the following methods of birth control unless she or her partner is surgically sterile or she is postmenopausal (hormone contraceptives [oral, implant, injection, patch, or ring], contraceptive sponge, double barrier [diaphragm or condom plus spermicide], or IUD;
- Contraindications to MRI such as claustrophobia or metal in their body;
- Subjects whose participation would cause them to exceed yearly radiation limits for research subjects
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Healthy Control population PKAB Subjects will be asked to complete both a 90 minute \[11C\]CFN and a 90 minute \[11C\]PKAB PET Imaging. Alcohol Use Disorder population completing Detoxification Detoxification Program Subjects will be asked to complete both 90 minute \[11C\]CFN and 90 minute \[11C\]PKAB PET Imaging after 1-3 days of a detoxification program. Healthy Control population CFN Subjects will be asked to complete both a 90 minute \[11C\]CFN and a 90 minute \[11C\]PKAB PET Imaging. Alcohol Use Disorder population completing Detoxification PKAB Subjects will be asked to complete both 90 minute \[11C\]CFN and 90 minute \[11C\]PKAB PET Imaging after 1-3 days of a detoxification program. Alcohol Use Disorder population completing Detoxification CFN Subjects will be asked to complete both 90 minute \[11C\]CFN and 90 minute \[11C\]PKAB PET Imaging after 1-3 days of a detoxification program.
- Primary Outcome Measures
Name Time Method Regional binding availability and volume of distribution of (Kappa-Opioid receptors) Between 3 to 6 weeks into alcohol cessation Time activity curves will be extracted from brain regions of interest during \[11C\]PKAB PET Imaging. AUD subjects will be asked to complete this 3 -6 weeks into alcohol cessation. Healthy control subjects will be matched based on sex(Male/Female), smoking status (current/former/nonsmoker), and BMI (kg/m\^2)
Change in Alcohol Craving Up to 1 month prior to initial imaging and up to 6 days into alcohol cessation Craving will be assessed with Alcohol Craving Scale (ACS, adapted from Singleton et al.63),
Range: 47 to 329, higher scores indicate higher craving to alcoholChange in Alcohol Use Up to 1 month prior to initial imaging and up to 6 days into alcohol cessation Assessed using the TimeLine Followback (TLFB)62 and BACtrack Skyn; AUD and Healthy controls will be asked to complete this paper questionnaire up to 1 month prior to CFN and PKAB PET Imaging and once again up to 6 days into alcohol cessation for AUD population.
Calendar style open ended.
Minimum 0 alcohol uses in past month -31 sittings of alcohol in past monthChange in Mood Up to 1 month prior to initial imaging and up to 6 days into alcohol cessation Mood, anhedonia symptoms will be assessed with the Center for Epidemiologic Studies Depression Scale (CES-D) Range : 0 to 60. Higher scores indicate more symptoms of depression.
Alcohol Cue Reactivity Craving Within first 6 days of abstinence Investigators will follow the paradigm developed for the NIAAA Human Laboratory Medication Screening Program (HLAB). In the paradigm, participants will be first exposed to a glass of water and then to their typical alcoholic beverage, separated by a 90 second rest period. They will be instructed to not drink but to sniff the beverages for a fixed duration. Immediately after, alcohol craving and beverage liking will be assessed. AUD subjects will be asked to complete this within first 6 days of abstinence. Healthy control subjects will be matched based on sex(Male/Female), smoking status (current/former/nonsmoker), and BMI (kg/m\^2)
Regional binding availability and volume of distribution of (Mu-Opioid receptors) Between 3 to 6 weeks into alcohol cessation Time activity curves will be extracted from brain regions of interest during \[11C\]CFN PET Imaging. AUD subjects will be asked to complete this 3 -6 weeks into alcohol cessation. Healthy control subjects will be matched based on sex(Male/Female), smoking status (current/former/nonsmoker), and BMI (kg/m\^2)
Change in Alcohol Withdrawal Up to 1 month prior to initial imaging and up to 6 days into alcohol cessation Withdrawal will be assessed using The Clinical Institute Withdrawal Assessment (CIWA-R)64. AUD and Healthy controls will be asked to complete this paper questionnaire up to 1 month prior to CFN and PKAB PET Imaging and once again up to 6 days into alcohol cessation for AUD population
Range: 0- 67, higher scores indicating more symptoms of withdrawal.
- Secondary Outcome Measures
Name Time Method Baseline Visual Attention Up to 3 months prior to initial imaging or on initial imaging day (depending hospital availability Identification Task - a computerized task to assess visual attention and vigilance. Response latency to identify card color (log10(ms)higher \~worse attention)
Range: 0 milliseconds - 30 minute times out.Test Executive Function Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) : Cogstate Groton Maze Learning Task - a computerized task to assess executive function and spatial problem solving. # of errors navigating a 'hidden' maze (5 trials; higher \~ worse executive function.
Range: 0-140 errors per trial, 0- 700 errors for all five trialsTest Visual Processing Speed Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) Cogstate Detection Task - a computerized task to assess psychomotor function and speed of processing. Visual -motor processing speed: response latency to detect a card flipped over (log10(ms); higher\~ worse processing speed).
Range: 0 milliseconds - 30 minute times out.Baseline Visual Learning Up to 3 months prior to initial imaging or on initial imaging day (depending hospital availability One Card Learning Task - a computerized task to assess visual learning and memory. Visual Learning: % of correctly identified repeat cards (arcsine% correct); higher \~ better learning.
Range: 66-88 cardsBaseline Executive Function Up to 3 months prior to initial imaging or on initial imaging day (depending hospital availability : Cogstate Groton Maze Learning Task - a computerized task to assess executive function and spatial problem solving. # of errors navigating a 'hidden' maze (5 trials; higher \~ worse executive function.
Range: 0-140 errors per trial, 0- 700 errors for all five trialsBaseline Visual Processing Speed Up to 3 months prior to initial imaging or on initial imaging day (depending hospital availability Cogstate Detection Task - a computerized task to assess psychomotor function and speed of processing. Visual -motor processing speed: response latency to detect a card flipped over (log10(ms); higher\~ worse processing speed).
Range: 0 milliseconds - 30 minute times out.Baseline Verbal Memory Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) Cogstate International Shopping List Task - a computerized task to assess verbal learning and memory.
# of correctly recalled items from a grocery list (3 trials). Verbal Recalled item from grocery list after delay (1 trial; higher \~better memory/recall)
Range: 0 to 36 errors (per trial), up to 108 errors for all 3 trials.Test Visual Attention Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) Identification Task - a computerized task to assess visual attention and vigilance. Response latency to identify card color (log10(ms)higher \~worse attention)
Range: 0 milliseconds - 30 minute times out.Baseline Working Memory One Back Up to 3 months prior to initial imaging or on initial imaging day (depending hospital availability One Back Task - computerized tasks to assess attention and working memory. Working memory: % of correctly identified cards that matched the card presented either one card previously (arcsine(% correct); Higher\~ better working memory
Range: ONB 24-31,Test Visual Learning Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) One Card Learning Task - a computerized task to assess visual learning and memory. Visual Learning: % of correctly identified repeat cards (arcsine% correct); higher \~ better learning.
Range: 66-88Baseline Working Memory Two Back Up to 3 months prior to initial imaging or on initial imaging day (depending hospital availability One Back Task - computerized tasks to assess attention and working memory. Working memory: % of correctly identified cards that matched the card presented either one card previously (arcsine(% correct); Higher\~ better working memory
Range: Two Back 24-32Test Working Memory Two Back Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) Two Back Task - computerized tasks to assess attention and working memory. Working memory: % of correctly identified cards that matched the card presented either one card previously (arcsine(% correct); Higher\~ better working memory
Range: Two Back 24-32Test Working Memory One Back Completed on second PKAB/CFN imaging day (Between 3 to 6 weeks into alcohol cessation) One Back Task - computerized tasks to assess attention and working memory. Working memory: % of correctly identified cards that matched the card presented either one card previously (arcsine(% correct); Higher\~ better working memory
Range: ONB 24-31
Trial Locations
- Locations (1)
Yale University
🇺🇸New Haven, Connecticut, United States