Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2008-1-11
pubmed:abstractText
Attention-deficit/hyperactivity disorder (ADHD) symptoms are associated with an increased risk of smoking, and genetic studies have identified similar candidate genes associated with both ADHD and smoking phenotypes. This paper addresses the question of whether ADHD symptoms interact with candidate gene variation to predict smoking risk. Participants were a subsample of individuals from the National Longitudinal Study of Adolescent Health (Add Health), a nationally representative sample of adolescents followed from 1995 to 2002. The sample analyzed included a subset from Add Health of 1,900 unrelated individuals with genotype data. Multiple logistic regression was used to examine relationships between self-reported ADHD symptoms, genotype, and lifetime history of regular smoking. Polymorphisms in the DRD2 gene and, among females, the MAOA gene interacted with retrospective reports of ADHD symptoms in contributing to risk for smoking. Trends were observed for interactions between the DRD4 gene and, among males, the MAOA gene and ADHD symptoms to predict smoking risk. No main effect for any of these polymorphisms was observed. We observed neither main effects nor interactions with CYP2A6, DAT, and SLC6A4 genes. These findings suggest that genotypes associated with catecholamine neurotransmission interact with ADHD symptoms to contribute to smoking risk.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aryl Hydrocarbon Hydroxylases, http://linkedlifedata.com/resource/pubmed/chemical/DRD3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/DRD4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Plasma Membrane Transport..., http://linkedlifedata.com/resource/pubmed/chemical/Mixed Function Oxygenases, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D2, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D3, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D4, http://linkedlifedata.com/resource/pubmed/chemical/SLC6A4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Plasma Membrane..., http://linkedlifedata.com/resource/pubmed/chemical/coumarin 7-hydroxylase
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1462-2203
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
117-27
pubmed:meshHeading
pubmed-meshheading:18188752-Adolescent, pubmed-meshheading:18188752-Adult, pubmed-meshheading:18188752-Aryl Hydrocarbon Hydroxylases, pubmed-meshheading:18188752-Attention Deficit Disorder with Hyperactivity, pubmed-meshheading:18188752-Comorbidity, pubmed-meshheading:18188752-Dopamine Plasma Membrane Transport Proteins, pubmed-meshheading:18188752-Female, pubmed-meshheading:18188752-Genetic Predisposition to Disease, pubmed-meshheading:18188752-Humans, pubmed-meshheading:18188752-Impulse Control Disorders, pubmed-meshheading:18188752-Longitudinal Studies, pubmed-meshheading:18188752-Male, pubmed-meshheading:18188752-Mixed Function Oxygenases, pubmed-meshheading:18188752-Polymorphism, Genetic, pubmed-meshheading:18188752-Receptors, Dopamine D2, pubmed-meshheading:18188752-Receptors, Dopamine D3, pubmed-meshheading:18188752-Receptors, Dopamine D4, pubmed-meshheading:18188752-Retrospective Studies, pubmed-meshheading:18188752-Risk Factors, pubmed-meshheading:18188752-Serotonin Plasma Membrane Transport Proteins, pubmed-meshheading:18188752-Smoking
pubmed:year
2008
pubmed:articleTitle
Interactions between genotype and retrospective ADHD symptoms predict lifetime smoking risk in a sample of young adults.
pubmed:affiliation
Department of Psychiatry and Behavioral Sciences, Duke University Medical Cneter, Durham, NC 27708, USA. mccle011@mc.duke.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural