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Sunday, March 4, 2007

Association of the neuronal nicotinic receptor 2 subunit gene (CHRNB2) with subjective responses to alcohol and nicotine

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Early View Published Online: 16 Jan 2007

Marissa A. Ehringer 1 2 *,
Hilary V. Clegg 1,
Allan C. Collins 1 3,
Robin P. Corley 1,
Thomas Crowley 4,
John K. Hewitt 1 3,
Christian J. Hopfer 4,
Kenneth Krauter 5,
Jeffrey Lessem 1,
Soo Hyun Rhee 1 3,
Isabel Schlaepfer 1 2,
Andrew Smolen 1,
Michael C. Stallings 1 3,
Susan E. Young 1,
Joanna S. Zeiger 1
1Institute for Behavioral Genetics, University of Colorado, Boulder, Colorado
2Department of Integrative Physiology, University of Colorado, Boulder, Colorado
3Department of Psychology, University of Colorado, Boulder, Colorado
4Department of Psychiatry, Division of Substance Dependence, University of Colorado School of Medicine, Denver, Colorado
5Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, Colorado
email: Marissa A. Ehringer (Marissa.Ehringer@colorado.edu)
Correspondence to Marissa A. Ehringer, University of Colorado, Institute for Behavioral Genetics 447 UCB, Boulder, CO 80309.

Funded by:

Colorado Tobacco Research Program IDEA; Grant Number: 2I-034
NIH; Grant Number: DA011015, DA012845, HD010333, EY012562, DA03194, MH001865, DA13956, DA015522

Keywords
CHRNA4 • CHRNB2 • nicotine • alcohol • genetic association

Abstract

Nicotine addiction and alcohol dependence are highly comorbid disorders that are likely to share overlapping genetic components.

We have examined two neuronal nicotinic receptor subunit genes (CHRNA4 and CHRNB2) for possible associations with nicotine and alcohol phenotypes, including measures of frequency of use and measures of initial subjective response in the period shortly after first using the drugs.

The subjects were 1,068 ethnically diverse young adults participating in ongoing longitudinal studies of adolescent drug behaviors at the University of Colorado, representing both clinical and community samples.

Analysis of six SNPs in the CHRNA4 gene provided modest support for an association with past 6 month use of alcohol in Caucasians (three SNPs with P < 0.08), but no evidence for an association with tobacco and CHRNA4 was detected.

However, a SNP (rs2072658) located immediately upstream of CHRNB2 was associated with the initial subjective response to both alcohol and tobacco. T

This study provides the first evidence for association between the CHRNB2 gene and nicotine- and alcohol-related phenotypes, and suggests that polymorphisms in CHRNB2 may be important in mediating early responses to nicotine and alcohol.