The overall goal of this proposal is to continue the ongoing PROSPECTIVE STUDY of high-risk adolescents and young adults from the COGA study to enhance our knowledge about genetic, behavioral and environmental risk factors that contribute to the development of heavy drinking, alcohol related problems, alcohol use disorders (AUDs), and related psychiatric conditions. The COGA study is unique in gathering important information from multiple domains across generations of well characterized, multi-ethnic families collected nationally. Data include psychiatric, electrophysiological, neuropsychological, environmental, and genetic factors gathered prospectively from families at high risk for AUDs and from comparison families. Parallel measures for these domains were gathered previously on the original proband parents and other biological relatives in addition to the adolescents and young adults who are the focus of our ongoing work. Data from the parental generation have been successfully used to identify numerous risk factors for heavier drinking and associated problems and have helped to identify genes related directiy to the risk for AUDs and associated characteristics (highest quantities consumed, craving, levels of response to alcohol). Our work has also identified genes that contribute to externalizing behaviors measured both through structured interviews and electrophysiological profiles. Thus, the proposed work presents the unique opportunity to observe the ways in which genetic variants, electrophysiological endophenotypes and behavioral characteristics identified In one generation may operate, in conjunction with the environment, during the developmental phases of adolescence and eariy adulthood of the next generation. This cross generational information may help identify additional behavioral and environmental characteristics associated with gene variation and other markers of risk, which in turn would enhance our understanding of a broader array of risk factors for AUDs.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Cooperative Clinical Research--Cooperative Agreements (U10)
Project #
5U10AA008401-25
Application #
8537105
Study Section
Special Emphasis Panel (ZAA1-CC)
Project Start
Project End
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
25
Fiscal Year
2013
Total Cost
$633,008
Indirect Cost
Name
Suny Downstate Medical Center
Department
Type
DUNS #
040796328
City
Brooklyn
State
NY
Country
United States
Zip Code
11203
Wetherill, Leah; Foroud, Tatiana; Goodlett, Charles (2018) Meta-Analyses of Externalizing Disorders: Genetics or Prenatal Alcohol Exposure? Alcohol Clin Exp Res 42:162-172
Dick, Danielle M (2018) Mapping Risk from Genes to Behavior: The Enduring and Evolving Influence of Irving Gottesman's Endophenotype Concept. Twin Res Hum Genet 21:306-309
Dick, Danielle M; Barr, Peter B; Cho, Seung Bin et al. (2018) Post-GWAS in Psychiatric Genetics: A Developmental Perspective on the ""Other"" Next Steps. Genes Brain Behav 17:e12447
Scarnati, Matthew S; Halikere, Apoorva; Pang, Zhiping P (2018) Using human stem cells as a model system to understand the neural mechanisms of alcohol use disorders: Current status and outlook. Alcohol :
Culverhouse, R C; Saccone, N L; Horton, A C et al. (2018) Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Mol Psychiatry 23:133-142
Prytkova, Iya; Goate, Alison; Hart, Ronald P et al. (2018) Genetics of Alcohol Use Disorder: A Role for Induced Pluripotent Stem Cells? Alcohol Clin Exp Res 42:1572-1590
Savage, Jeanne E; Salvatore, Jessica E; Aliev, Fazil et al. (2018) Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population-Based and Clinically Ascertained Samples. Alcohol Clin Exp Res 42:520-530
van der Vaart, Andrew; Meng, Xianfang; Bowers, M Scott et al. (2018) Glycogen synthase kinase 3 beta regulates ethanol consumption and is a risk factor for alcohol dependence. Neuropsychopharmacology 43:2521-2531
Agrawal, A; Chou, Y-L; Carey, C E et al. (2018) Genome-wide association study identifies a novel locus for cannabis dependence. Mol Psychiatry 23:1293-1302
McCutcheon, Vivia V; Agrawal, Arpana; Kuo, Sally I-Chun et al. (2018) Associations of parental alcohol use disorders and parental separation with offspring initiation of alcohol, cigarette and cannabis use and sexual debut in high-risk families. Addiction 113:336-345

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