z-logo
open-access-imgOpen Access
Haplotypes with Copy Number and Single Nucleotide Polymorphisms in CYP2A6 Locus Are Associated with Smoking Quantity in a Japanese Population
Author(s) -
Natsuhiko Kumasaka,
Masayuki Aoki,
Yukinori Okada,
Atsushi Takahashi,
Kouichi Ozaki,
Taisei Mushiroda,
Tomomitsu Hirota,
Mayumi Tamari,
Toshihiro Tanaka,
Yusuke Nakamura,
Naoyuki Kamatani,
Michiaki Kubo
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0044507
Subject(s) - single nucleotide polymorphism , haplotype , genetics , locus (genetics) , biology , cyp2a6 , snp , genome wide association study , allele , population , genotype , gene , medicine , environmental health , microsome , cyp1a2 , in vitro
Smoking is a major public health problem, but the genetic factors associated with smoking behaviors are not fully elucidated. Here, we have conducted an integrated genome-wide association study to identify common copy number polymorphisms (CNPs) and single nucleotide polymorphisms (SNPs) associated with the number of cigarettes smoked per day (CPD) in Japanese smokers (  = 17,158). Our analysis identified a common CNP with a strong effect on CPD (rs8102683;) in the 19q13 region, encompassing the CYP2A6 locus. After adjustment for the associated CNP, we found an additional associated SNP (rs11878604;) located 30 kb downstream of the CYP2A6 gene. Imputation of the CYP2A6 locus revealed that haplotypes underlying the CNP and the SNP corresponded to classical, functional alleles of CYP2A6 gene that regulate nicotine metabolism and explained 2% of the phenotypic variance of CPD (ANOVA-test). These haplotypes were also associated with smoking-related diseases, including lung cancer, chronic obstructive pulmonary disease and arteriosclerosis obliterans.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom