Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence
Alcohol dependence frequently co-occurs with cigarette smoking, another common addictive behavior. Evidence from genetic studies demonstrates that alcohol dependence and smoking cluster in families and have shared genetic vulnerability. Recently a candidate gene study in nicotine dependent cases and...
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Veröffentlicht in: | Molecular psychiatry 2009-05, Vol.14 (5), p.501-510 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Alcohol dependence frequently co-occurs with cigarette smoking, another common addictive behavior. Evidence from genetic studies demonstrates that alcohol dependence and smoking cluster in families and have shared genetic vulnerability. Recently a candidate gene study in nicotine dependent cases and nondependent smoking controls reported strong associations between a missense mutation (rs16969968) in exon 5 of the
CHRNA5
gene and a variant in the 3′-UTR of the
CHRNA3
gene and nicotine dependence. In this study we performed a comprehensive association analysis of the
CHRNA5–CHRNA3–CHRNB4
gene cluster in the Collaborative Study on the Genetics of Alcoholism (COGA) families to investigate the role of genetic variants in risk for alcohol dependence. Using the family-based association test, we observed that a different group of polymorphisms, spanning
CHRNA5-CHRNA3
, demonstrate association with alcohol dependence defined by
Diagnostic and Statistical Manual of Mental Disorders
, 4th edn (DSM-IV) criteria. Using logistic regression we replicated this finding in an independent case-control series from the family study of cocaine dependence. These variants show low linkage disequilibrium with the SNPs previously reported to be associated with nicotine dependence and therefore represent an independent observation. Functional studies in human brain reveal that the variants associated with alcohol dependence are also associated with altered steady-state levels of
CHRNA5
mRNA. |
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ISSN: | 1359-4184 1476-5578 |
DOI: | 10.1038/mp.2008.42 |