COGA (Collaborative Study On the Genetics of Alcoholism) focuses on the identification and characterization of gene variants that contribute to the etiology of alcohol abuse, alcoholism and comorbid disorders, a goal more readily attained if clinical data and biological materials derived from a large number of subjects are ultimately shared by many researchers. This proposal summarizes the current activities of the Nl/'OWCOGA Sharing Repository (NCSR) and describes ongoing plans to expand its scope of activities to better serve the goals of the NIAAA and COGA. The COGA biosamples are housed in the Rutgers University Cell and DNA Repository (RUCDR), under the direction of Dr. Jay Tischfleld. For neariy twenty years, the NCSR has produced lymphoblast cell lines (LCLs), DNA from blood and LCLs, and (in the last two years) RNA from LCLs. The biosamples are available to COGA investigators and, along with the associated clinical data, to NIAAA-approved researchers outside of COGA. Genotyping of DNA provided by the NCSR produces data that will continue to Identify gene variants influencing endophenotypes and clinical phenotypes related to alcohol dependence and corresponding vulnerabilities, while the LCLs and blood-derived DNA provide a unique platform for functional genomic and epigenomic studies, respectively. The data management component of NCSR maintains an """"""""anonymized"""""""" database on family structure, age, sex, clinical status, and diagnoses (described in Data Management, Section V). COGA Pis and NIAAA-approved researchers may access data related to NCSR biosamples through a secure web site (www.niaaaqenetics.orq/).

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Cooperative Clinical Research--Cooperative Agreements (U10)
Project #
5U10AA008401-22
Application #
8137974
Study Section
Special Emphasis Panel (ZAA1)
Project Start
Project End
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
22
Fiscal Year
2010
Total Cost
$442,999
Indirect Cost
Name
Suny Downstate Medical Center
Department
Type
DUNS #
040796328
City
Brooklyn
State
NY
Country
United States
Zip Code
11203
Su, Jinni; Kuo, Sally I-Chun; Aliev, Fazil et al. (2018) Influence of Parental Alcohol Dependence Symptoms and Parenting on Adolescent Risky Drinking and Conduct Problems: A Family Systems Perspective. Alcohol Clin Exp Res 42:1783-1794
Miller, M L; Ren, Y; Szutorisz, H et al. (2018) Ventral striatal regulation of CREM mediates impulsive action and drug addiction vulnerability. Mol Psychiatry 23:1328-1335
Olfson, Emily; Bloom, Joseph; Bertelsen, Sarah et al. (2018) CYP2A6 metabolism in the development of smoking behaviors in young adults. Addict Biol 23:437-447
Salvatore, Jessica E; Dick, Danielle M (2018) Genetic influences on conduct disorder. Neurosci Biobehav Rev 91:91-101
Edenberg, Howard J; McClintick, Jeanette N (2018) Alcohol Dehydrogenases, Aldehyde Dehydrogenases, and Alcohol Use Disorders: A Critical Review. Alcohol Clin Exp Res 42:2281-2297
Edwards, Alexis C; Deak, Joseph D; Gizer, Ian R et al. (2018) Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. Alcohol Clin Exp Res 42:2349-2359
Korhonen, Tellervo; Sihvola, Elina; Latvala, Antti et al. (2018) Early-onset tobacco use and suicide-related behavior - A prospective study from adolescence to young adulthood. Addict Behav 79:32-38
Wang, Kesheng; Chen, Xue; Ward, Stephen C et al. (2018) CYP2A6 is associated with obesity: studies in human samples and a high fat diet mouse model. Int J Obes (Lond) :
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

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