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Involvement of the Septal Nuclei of the Human Brain in Alcohol Use Disorder

A

Anders Fink-Jensen, MD, DMSci

Status

Enrolling

Conditions

Alcohol Use Disorder

Treatments

Other: Brain imaging

Study type

Interventional

Funder types

Other

Identifiers

NCT06866379
The septum study

Details and patient eligibility

About

Alcohol activates reward systems in different brain areas, i.e., the nucleus accumbens, dorsal striatum, extended amygdala, and prefrontal cortex. These areas are all part of the reward neurocircuitry, which plays an important role in the development of addiction.

A former study performed on rodents has shown that a specific area of the forebrain, the septal nuclei, is associated with the feeling of reward and, hence, addiction when stimulated. However, whether the septal area is involved in reward and addiction in humans is sparsely investigated.

The purpose of this brain-imaging study is to assess how the septal nuclei react to alcohol-related pictures shown to participants diagnosed with alcohol use disorder while lying in an MRI scanner, compared to people without a diagnosis of alcohol use disorder. This might give us a better understanding of how the septal nuclei is involved in reward and addiction.

Full description

This is a comparative, non-interventional, case-control, brain imaging study using the ALCUE paradigm to investigate the neuro-anatomical underpinings of AUD during a fMRI-scan. The contrast used for the fMRI scans is the BOLD signal which measures the ratio of oxygenated to deoxygenated blood in the brain as a measurement of neural activity.

The study will conclude after the last participant with AUD succesfully has undergone the fMRI scan, and will include 50 participants in total: 25 participants diagnosed with AUD and 25 participants without AUD (data from a previous brain imaging study). Written informed consent will be collected, before any trial activities are performed.

Enrollment

25 estimated patients

Sex

All

Ages

30 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with alcohol use disorder (AUD) according to DSM-5, and alcohol dependence according to ICD-10
  • An Alcohol Use Disorder Identification Test (AUDIT) score ≥ 15
  • At least six heavy drinking days for the last 30 days, measured with the Time Line Follow Back (TLFB) method

Exclusion criteria

  • Diagnosis of schizophrenia spectrum disorder, paranoid psychosis, bipolar disorder, or mental retardation
  • Previous or current substance use disorder other than AUD and nicotine use disorder
  • History of alcohol withdrawal seizures within the past 5 years
  • Alcohol withdrawal symptoms defined as a CIWA-Ar score > 9 at screening or at the fMRI session
  • Treatment with chlordiazepoxide or other benzodiazepine within the past 30 days
  • Other pharmacological treatment for AUD within the past 30 days
  • Treatment with GLP-1 analogues within the last 6 months
  • Urine tests positive for psychoactive drugs (cocaine, amphetamine, TCH, methadone, opioids, and benzodiazepines) at screening
  • DUDIT score ≥ 2/6 for females/males
  • Contraindications for undergoing an fMRI scan (magnetic implants, metal splinters, pacemaker, claustrophobia, etc.)
  • Females of childbearing potential who are either pregnant, breastfeeding or have the intention of becoming pregnant within the next month or are not using contraception appropriate for participating in a clinical study
  • Pregnancy (positive urine pregnancy test)
  • Unable to speak or understand Danish
  • Any condition that the investigator feels would interfere with trial participation

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Participants with AUD
Experimental group
Description:
Participants diagnosed with alcohol use disorder participating in one fMRI brain scan.
Treatment:
Other: Brain imaging

Trial contacts and locations

1

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Central trial contact

Anders Fink-Jensen, Professor; Mette K Klausen, MD, PhD

Data sourced from clinicaltrials.gov

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