Eligibility

Ages Eligible for Study

18 years to 25 years

Genders Eligible for Study

Both

Keywords

Reward Circuitry, Impulsivity, Family History of Alcoholism, and NMDA/DA Interactions

Sponsors

Other

Yale University

Inclusion Criteria

- Biological father with a history of Alcoholism

- A least 1 other first- or second-degree relative with a history of Alcoholism.

Exclusion Criteria

- Cannot be an only child

- A diagnosis of DSM-IV-TR Axis I psychotic disorders screened with the Mini
International Neuropsychiatric Interview (MINI), done in the BARCS study (with the
exception of Alcohol Abuse)

- Report of psychotic disorder in a 1º relative

- Prenatal exposure to alcohol (mother reported to drink 3 or more drinks on an
occasion or more than 3 times per month during pregnancy

- Not speaking English fluently or being a non-native English speaker, or being
educated in a primary language other than English >grade 1

- Mental retardation (Full Scale IQ 30 minutes or concussion in last
30 days

- Presence or history of any medical/neurologic illness that may affect brain
physiology (e.g., epilepsy, Multiple Sclerosis), including focal brain lesion seen on
structural MRI (all structural scans are read by a licensed radiologist)

- Current pregnancy (all females will be tested with urine screens on the day of MRI)

- Any positive alcohol screen will result in exclusion

- Inability to comprehend the consent form appropriately

- Other specific fMRI exclusions include metal devices, clips or fragments in body
(orbital x-ray performed if needed)

- Female participants under 125 pounds will be excluded from participating due to the
strength and side effects in this segment of the population.

Detailed Description

This project compares Family History Positive (FHP) for alcoholism subjects to matched Family History Negative (FHN) subjects derived from the project Principal Investigator's National Institute on Alcohol Abuse and Alcoholism-funded longitudinal study of drinking behavior in a 2000 college freshman population (known as the Brain and Alcohol Research in College Students study (BARCS)). The age of these subjects is a valuable one at which to capture the transition from harmful use to abuse/dependence. This project explores the effects of memantine in a double-blind, randomized, counterbalanced manner on alcoholism risk-relevant tasks. More specifically, this project studies functional MRI tasks related to different aspects of reward and/or impulsivity-related behavior in different contexts, compares the underlying neural circuitry across tasks, and uses a pharmacologic probe of the glutamatergic system to examine NMDA/DA interactions. The combined measures provide the opportunity to advance our understanding of specific aspects of brain function related to familial alcoholism vulnerability in an already well-characterized population as some members evolve into alcohol abuse. In addition to conventional within-task analyses, functional network connectivity and allied approaches will be used to examine brain networks across tasks. The investigators will study adult male and female subjects in equal numbers who are either offspring of an alcoholic parent or are FHN matched controls. The investigators will recruit and assess a total of 84 (42 FHP and 42 matched FHN) subjects between the ages of 18-21 years on initial BARCS contact. The investigators will use 4 cognitive tasks during the functional MRI (fMRI) which include: 1) a Monetary Incentive Delay Task that distinguishes networks engaged in motivational (anticipation) and consummatory (outcome) components of reward processing; 2) a Go/No-Go Task that measures the ability to inhibit response to a pre-potent stimulus; 3) an Alcohol Cue Reactivity Task that examines Nucleus Accumbens response to alcohol-related versus matched soft drink stimuli; and 4) a Pavlovian-to-Instrumental Transfer (PIT) Task that dissects a component of the Monetary Incentive Delay (MID) Task, and provides an imaging assay of a transfer-like process that can be related to real-world drinking behavior, thus informing upon and extending the key findings from CTNA-2.