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Metabolism in the Human Brain Following Consumption of a Keto-ester in Alcohol Use Disorder (AUD) With Proton Magnetic Resonance Spectroscopic Imaging (MRSI)

Metabolism in the Human Brain Following Consumption of a Keto-ester in Alcohol Use Disorder (AUD) With Proton Magnetic Resonance Spectroscopic Imaging (MRSI)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05937893
Enrollment
12
Registered
2023-07-10
Start date
2023-08-14
Completion date
2024-05-15
Last updated
2024-12-11

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

Conditions

Alcohol Use Disorder, BHB Transport

Keywords

BHB, AUD

Brief summary

The objective of this study is to determine whether BHB levels in the brain will be positively associated with alcohol consumption, due to hypothesized enhancement of BHB transport into the brain.

Detailed description

The primary objective of this study is to determine whether BHB levels in the brain will be positively associated with alcohol consumption, due to hypothesized enhancement of BHB transport into the brain. Furthermore, BHB levels in identified brain regions will be compared against measures of craving. The secondary objective of this study is to investigate if GABA levels will be elevated in key brain regions relative to the baseline scan in AC subjects due to preferential BHB metabolism. The goal is to acquire preliminary data to apply for an R01 or equivalent grant submission to pursue this metabolic therapy in greater detail using the state-of-the-art MRSI platform at Yale University to study alcohol use disorders.

Interventions

OTHERKeto-ester followed by Magnetic Resonance Spectroscopic Imaging (MRSI) scans

Following baseline scans, the participant will orally consume the keto-ester, for subsequent scans which will include repeated BHB MRSI acquisitions to dynamically measure BHB labeling in the brain, followed by a final GABA MRSI acquisition.

Sponsors

Yale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* For AUD patients: individuals assessed to be with mild to - medium severity according to the DSM-5 criteria. * For non-dependent heavy at-risk drinkers: must be Individuals who consume more than 14 drinks per week for men or more than 8 drinks per week for women, for at least the last 2 months. * For healthy controls: must be light drinkers not dependent on alcohol, who consume fewer than 2 drinks per week for at least the last 6 months. * English speaking * Can read and understand a study the consent form

Exclusion criteria

* Non-English speaking * Unable to read and understand the consent form * History of alcohol withdrawal in the last 12 months. This will reduce chances of a volunteer having withdrawal symptoms in the middle of the experiment. * Participants with a history of psychiatric conditions (that include PTSD, schizophrenia, and bipolar disorders), or a history of neurological conditions * Women who test positive on a pregnancy test collected on either the screening visit or day of the study. * Healthy subjects identified with substance use with the exception of tobacco and alcohol will be excluded. * AC subjects identified with substance use, with the exception of tobacco, alcohol, and mild cannabis use disorder (based on the DSM-5 criteria during the medical history) in the last 6 months, will be excluded. * Persons unable to refrain from alcohol use for 48 hours and undergo a 10-hour fast prior to the study

Design outcomes

Primary

MeasureTime frameDescription
Change in BHB levels in the brainApproximately 90 minutes after Baseline Assessmentβ-hydroxybutyrate blood levels in the brain will be assessed via MRSI.

Secondary

MeasureTime frameDescription
Change in GABA levels in the brainApproximately 90 minutes after Baseline AssessmentGABA levels will be assessed in the brain via MRSI to determine if they are elevated in key brain regions relative to the baseline scan.

Countries

United States

Outcome results

None listed

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