Adolescence is a period when many individuals begin to experiment with alcohol, with some progressing rapidly to abusive drinking. The acute problems associated with heavy adolescent alcohol use (e.g., alcohol poisoning, sexual victimization, automobile accidents) have been well documented; less certain is whether adolescent alcohol use also has long-term consequences. Three recent reviews of the relevant literature have come to similar conclusions: adolescent drinking is associated with adult functioning, but the existing literature does not tell us whether these associations are causal or whether the consequences of adolescent drinking are long-lasting. We propose to address these limitations with a prospective study of a unique cohort of twins. These twins were initially assessed at age 17, at the early stages of alcohol use, and again at age 20, the period in adolescence when alcohol use peaks. They were subsequently assessed at ages 24 and 29, a period characterized by life-role transition. We now propose to assess them at mid-life (average age of 42 years), a developmental period characterized by stability and for most a moderation of youthful patterns of heavy drinking. The in-person assessment will cover 4 major domains of functioning: 1) mental health, including substance use and abuse, 2) physical health and behavior, 3) neurocognitive function, and 4) psychosocial outcomes including educational and occupational achievement and relationship quality. We estimate that 1130 twins will participate (greater than 90% of the surviving members of the original cohort) in the in-person assessment and that 910 of their spouses/partners will also complete a brief mail survey. Analysis of the data will document the range of adult outcomes associated with adolescent drinking and evaluate three alternative models to account for these effects: 1) the factors that lead to early and heavy drinking in adolescence also increase the likelihood of deficits in adulthood (i.e., confounding), 2) adolescent heavy drinkers tend to become adult heavy drinkers (i.e., drinking persistence), and 3) adolescent drinking upsets the normal course of adult. The innovative cotwin control design, which controls for genetic and shared environmental factors on outcomes, will help isolate possible causal effects of adolescent drinking on midlife functioning. The extensive earlier assessments of this cohort will provide a wealth of information for propensity score estimation to further control for confounding by early indicators of risk (e.g., family history, personality) and provide comprehensive assessments of drinking exposure in early adulthood. Further, we will have an opportunity to investigate whether gender moderates the association of adolescent drinking with adult outcomes. The results of this study will provide essential information about the long-term consequences of adolescent drinking on adult mental and physical health and general psychosocial functioning and determine whether the potentially harmful consequences of adolescent drinking might be ameliorated by drinking desistence or prevented by social factors.

Public Health Relevance

There is considerable public health concern over the consequences of the early initiation and rapid escalation in drinking that can occur in adolescence. While we know much about the short-term consequences of adolescent drinking, we know relatively little about whether there are also long-term consequences, and, if there are, how those consequences might be ameliorated. We will address this gap in knowledge by completing a mid-life assessment covering mental health, physical, neurocognitive and social functioning of a large cohort of twins, first assessed at age 17, and determining the consequences of adolescent drinking for mid-life functioning and whether those consequences are mitigated by drinking desistence.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AA009367-25
Application #
9671329
Study Section
Behavioral Genetics and Epidemiology Study Section (BGES)
Program Officer
Castle, I-Jen
Project Start
1992-09-01
Project End
2021-03-31
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
25
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Goodman, Rebecca J; Samek, Diana R; Wilson, Sylia et al. (2018) Close relationships and depression: A developmental cascade approach. Dev Psychopathol :1-15
Elkins, Irene J; Saunders, Gretchen R B; Malone, Stephen M et al. (2018) Mediating pathways from childhood ADHD to adolescent tobacco and marijuana problems: roles of peer impairment, internalizing, adolescent ADHD symptoms, and gender. J Child Psychol Psychiatry 59:1083-1093
Elkins, Irene J; Saunders, Gretchen R B; Malone, Stephen M et al. (2018) Associations between childhood ADHD, gender, and adolescent alcohol and marijuana involvement: A causally informative design. Drug Alcohol Depend 184:33-41
Samek, Diana R; Hicks, Brian M; Durbin, Emily et al. (2018) Codevelopment Between Key Personality Traits and Alcohol Use Disorder From Adolescence Through Young Adulthood. J Pers 86:261-282
Park, Jun Young; Wu, Chong; Basu, Saonli et al. (2018) Adaptive SNP-Set Association Testing in Generalized Linear Mixed Models with Application to Family Studies. Behav Genet 48:55-66
Bornovalova, Marina A; Verhulst, Brad; Webber, Troy et al. (2018) Genetic and environmental influences on the codevelopment among borderline personality disorder traits, major depression symptoms, and substance use disorder symptoms from adolescence to young adulthood. Dev Psychopathol 30:49-65
Lee, James J; McGue, Matt; Iacono, William G et al. (2018) The accuracy of LD Score regression as an estimator of confounding and genetic correlations in genome-wide association studies. Genet Epidemiol 42:783-795
Smit, Dirk J A; Wright, Margaret J; Meyers, Jacquelyn L et al. (2018) Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Hum Brain Mapp 39:4183-4195
Harper, Jeremy; Malone, Stephen M; Iacono, William G (2017) Testing the effects of adolescent alcohol use on adult conflict-related theta dynamics. Clin Neurophysiol 128:2358-2368
Clark, Shaunna L; McClay, Joseph L; Adkins, Daniel E et al. (2017) Deep Sequencing of 71 Candidate Genes to Characterize Variation Associated with Alcohol Dependence. Alcohol Clin Exp Res 41:711-718

Showing the most recent 10 out of 37 publications