Alcohol initiation at an early age is associated with numerous negative outcomes, including a significant increase in the risk of developing an alcohol-use disorder later in life. Vulnerability for early misuse and other problematic alcohol use behaviors have been linked to individual differences in brain function. However, few studies have sought to identify brain-based predictors (?neuromarkers?) of alcohol use behaviors in youth. Identification of brain-based predictors of alcohol use behaviors in youth is essential for the development of more effective early prevention and intervention efforts. This proposal combines machine learning and longitudinal modeling approaches to 1) identify neural networks predictive of early alcohol initiation and misuse and 2) chart the developmental trajectories of these networks over time in a large sample of youth (N>3,000) using data from three unique, proprietary and completed datasets. Neural networks conferring vulnerability for alcohol use behaviors during adolescence will be identified using connectome-based predictive modeling (CPM). CPM is a machine-learning method of generating behavioral predictions from individual patterns of brain organization; i.e., functional connectivity matrices. Unlike traditional machine learning approaches, CPM is entirely data-driven and requires no a priori selection of brain regions or networks. As such, CPM is both a predictive tool and a method of identifying networks that underlie specific behaviors; i.e., neuromarkers. CPM has been successfully used to predict complex behaviors including future abstinence and other addiction-relevant phenotypes. This proposal will use CPM to identify neuromarkers of alcohol initiation and predict transitions to risky drinking in youth (AIM 1). Quantification of changes in brain function, e.g., growth curve trajectory analysis, is central to the characterization of developmental phenomena. Analyses of developmental trajectories can be used to identify particularly sensitive growth periods, detect variations that may signal risk, define modifiable targets, and monitor the impact of environment and interventions on development. While extant data indicate alcohol-related alterations in neural development, very few studies have assessed interactions between neurodevelopmental trajectories over time and alcohol-use behaviors. Developmental trajectories of identified networks in relation to alcohol use behaviors over time will be assessed using multilevel modeling (AIM 2). This proposal represents the first attempt to identify neural networks predictive of alcohol-initiation and risky drinking using a wholly data- driven, machine learning approach in a large sample of youth and does so using existing data. This is a critical step toward identifying a reliable predictor of alcohol initiation in youth and will shed light on individual difference factors representing vulnerability for misuse. Such predictors are needed to understand the developmental trajectories of alcohol phenotypes and to inform early risk models and preventative intervention efforts.

Public Health Relevance

Alcohol is the most commonly used substance in youth, and earlier ages of alcohol initiation are associated with increased likelihoods of alcohol-use disorder later in life. This project will identify brain networks that predict alcohol initiation and misuse?and chart the developmental trajectories of those networks over time? using existing neuroimaging data from three unique longitudinal datasets (N>3,000). Identification of brain- based predictors of alcohol initiation and misuse will aid in the development of targeted prevention and intervention efforts to address alcohol problems in youth.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Research Project (R01)
Project #
1R01AA027553-01
Application #
9713715
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Matochik, John A
Project Start
2019-06-01
Project End
2023-02-28
Budget Start
2019-06-01
Budget End
2020-02-29
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Yale University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520