Examination of Rare Missense Variants in the CHRNA5-A3-B4 Gene Cluster to Level of Response to Alcohol in the San Diego Sibling Pair Study
Reprint requests: Hélène Choquet, PhD, Center for Cerebrovascular Research, University of California, San Francisco, 1001 Potrero Avenue, Box-1363, Building 10, 2nd Floor, Room 1207, San Francisco, CA 94110;
Tel.: 415-206-4701; Fax: 415-206-8907; E-mail: ChoquetH@anesthesia.ucsf.edu
Common variants in the CHRNA5-A3-B4 gene cluster have been shown to be associated with nicotine dependence and alcohol use disorders (AUDs) and related traits, including the level of response (LR) to alcohol. Recently, rare variants (MAF < 0.05) in CHRNB4 have been reported to be associated with a decreased risk of developing nicotine dependence. However, the role of rare variants in the CHRNA5-A3-B4 gene cluster to the LR to alcohol has not yet been established.
To determine whether rare variants in the CHRNA5-A3-B4 gene cluster contribute to the LR to alcohol, the coding regions of these 3 genes were sequenced in 538 subjects from the San Diego Sibling Pair study.
The analyses identified 16 rare missense variants, 9 of which were predicted to be damaging using in silico analysis tools. Carriers of these variants were compared to noncarriers using a family-based design for each gene and for the gene cluster as a whole. In these analyses, a CHRNA5 carrier status was significantly associated with the phenotype related to the feeling of intoxication experienced during the alcohol challenge (p = 0.039).
These results indicate that rare genetic variation in the CHRNA5-A3-B4 gene cluster contributes modestly to the LR to alcohol in the San Diego Sibling Pair study and may protect against AUDs. However, replication studies are needed to confirm our findings.