The Nuclear Transcription Factor PKNOX2 Is a Candidate Gene for Substance Dependence in European-Origin Women
Year: 2011
Type: article
Study design: Observational Study
Abstract: Substance dependence or addiction is a complex environmental and genetic disorder that results in serious health and socio-economic consequences. Multiple substance dependence categories together, rather than any one individual addiction outcome, may explain the genetic variability of such disorder. In our study, we defined a composite substance dependence phenotype derived from six individual diagnoses: addiction to nicotine, alcohol, marijuana, cocaine, opiates or other drugs as a whole. Using data from several genomewide case-control studies, we identified a strong (Odds ratio = 1.77) and significant (p-value = 7E-8) association signal with a novel gene, PBX/knotted 1 homeobox 2 (PKNOX2), on chromosome 11 with the composite phenotype in European-origin women. The association signal is not as significant when individual outcomes for addiction are considered, or in males or African-origin population. Our findings underscore the importance of considering multiple addiction types and the importance of considering population and gender stratification when analyzing data with heterogeneous population.
Source: PLoS ONE
Institutions: Yale University, University of Florida
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,382
Awards: G2146332128, Study of Addiction: Genetics and Environment, Methodological Research on Substance Use, The Collaborative Genetic Study of Nicotine Dependence, G4503763930, Genome Wide Association Coordinating Center, JH/CIDR Genotyping for Genome-Wide Association Studies, G6134854566, FAMILY STUDY OF COCAINE DEPENDENCE, Research Training in Mental Health Epidemiology, G7093047072, G746875028, G7522350138, G8267674335, Analysis of Genomic Data for Complex Traits, G8924909668, G9000024769, G9000176579, Collaborative Study on the Genetics of Alcoholism (COGA).
OpenAlex ID: W1967647124
