期刊
JOURNAL OF MEDICAL GENETICS
卷 51, 期 5, 页码 327-333出版社
BMJ PUBLISHING GROUP
DOI: 10.1136/jmedgenet-2013-102151
关键词
-
资金
- National Institutes of Health [P42 ES010349, R01 CA107431]
Background The high prevalence of tobacco use in some developing nations, including Bangladesh, poses several public health challenges for these populations. Smoking behaviour is determined by genetic and environmental factors; however, the genetic determinants of smoking behaviour have not been previously examined in a Bangladeshi or South Asian population. We performed a genome-wide association study (GWAS) of tobacco smoking behaviour among a population-based sample of 5354 (2035 ever smokers and 3319 never smokers) men and women in Bangladesh. Methods Genome-wide association analyses were conducted for smoking initiation (ever vs never smokers), smoking quantity (cigarettes per day), age of smoking initiation, and smoking cessation (former vs current smokers). Sex-stratified associations were performed for smoking initiation. Results We observed associations for smoking initiation in the SLC39A11 region at 17q21.31 (rs2567519, p=1.33x10(-7)) among men and in the SLCO3A1 region at 15q26 (rs12912184, p=9.32x10(-8)) among women. Conclusions These findings suggest possible underlying mechanisms related to solute carrier transporter genes, which transport neurotransmitters, nutrients, heavy metals and other substrates into cells, for smoking initiation in a South Asian population in a sex-specific pattern. Genetic markers could have potential translational implications for the prevention or treatment of tobacco use and addiction in South Asian populations and warrant further exploration.
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