Sex Differences in Risk for Alcohol Abuse

Purpose

This study will determine the neural and hormonal mechanisms underlying sex differences in sensitivity to the disinhibiting effects of alcohol in heavy drinkers.

Condition

  • Alcohol Abuse

Eligibility

Eligible Ages
Between 21 Years and 29 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • heavy drinking - Alcohol Use Disorder Identification Test score above 7 - right-handed - BMI between 19 and 26 - high school education - fluent in English - women must have regular menstrual cycles - not using hormonal contraceptives

Exclusion Criteria

  • drug use disorder (SCID, DSM-5), other than nicotine or caffeine - meets withdrawal criteria - history of physical or psychiatric disease - contraindication for fMRI - pregnant or breastfeeding - smoking more than 5 cigarettes per day

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover Assignment
Primary Purpose
Basic Science
Masking
Single (Participant)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Alcohol, then saline, then alcohol, then saline
Participants first received alcohol (60mg%) intravenously and then 24-48 hours later they received saline intravenously. Two weeks later, they again received alcohol (60mg%) intravenously and then 24 - 48 hours later they received saline intravenously.
  • Drug: Alcohol
    Alcohol will be administered by IV infusion (60mg%).
  • Drug: Saline
    Saline is administered as the placebo
Experimental
Saline, then alcohol, then saline, then alcohol
Participants first received saline intravenously and then 24-48 hours later they received alcohol (60mg%) intravenously. Two weeks later, they again received saline intravenously and then 24 - 48 hours later they received alcohol (60mg%) intravenously.
  • Drug: Alcohol
    Alcohol will be administered by IV infusion (60mg%).
  • Drug: Saline
    Saline is administered as the placebo

Recruiting Locations

More Details

NCT ID
NCT04543942
Status
Completed
Sponsor
Mark Fillmore

Detailed Description

Alcohol abuse inflicts enormous physical, emotional, and financial burdens on the individual and society at large. Knowing who is at risk for alcohol abuse, and why, is crucial for the development of effective prevention and treatment strategies. Alcohol abuse has been traditionally considered a male-oriented problem and as a consequence research on risk factors specific to women has been minimal. However, the sex gap in substance abuse is closing rapidly, and findings from both animal and human studies suggest that females are actually more vulnerable to drug use than males. As such, there is an urgent need to identify sex differences in risk factors for alcohol abuse in order to develop sex-specific prevention and treatment efforts. One clear candidate risk factor is poor inhibitory control, both in terms of baseline levels of inhibition and sensitivity to the disinhibiting effects of alcohol. Recent studies suggest that sex hormones affect inhibitory control in drug-free individuals, potentially contributing to sex differences in baseline levels of inhibition. However, the degree to which fluctuations in sex hormones influence sex differences in inhibition-related brain function in sober and intoxicated individuals is not known. The proposed project will determine the neural and hormonal mechanisms underlying sex differences in sensitivity to the disinhibiting effects of alcohol in heavy drinkers. The overall objective of the research is to identify hormonal determinants of alcohol effects on brain activation during response inhibition (BARI) in young adult female and male drinkers. BARI will be assessed using functional magnetic resonance imaging (fMRI) during performance of the stop signal task. This task reliably activates right-lateralized prefrontal regions implicated in inhibitory control. This study will assess BARI during IV alcohol (60mg%) and saline infusion in women during the early follicular and mid-luteal phases and in men at matched intervals.