Center for Health Sciences, Policy Division, SRI International, Menlo Park, CA, USA.
Transl Psychiatry. 2012 May 22;2(5):e119. doi: 10.1038/tp.2012.41.
The identification and exploration of genetic loci that influence smoking behaviors have been conducted primarily in populations of the European ancestry. Here we report results of the first genome-wide association study meta-analysis of smoking behavior in African Americans in the Study of Tobacco in Minority Populations Genetics Consortium (n = 32,389). We identified one non-coding single-nucleotide polymorphism (SNP; rs2036527[A]) on chromosome 15q25.1 associated with smoking quantity (cigarettes per day), which exceeded genome-wide significance (β = 0.040, s.e. = 0.007, P = 1.84 × 10(-8)). This variant is present in the 5'-distal enhancer region of the CHRNA5 gene and defines the primary index signal reported in studies of the European ancestry. No other SNP reached genome-wide significance for smoking initiation (SI, ever vs never smoking), age of SI, or smoking cessation (SC, former vs current smoking). Informative associations that approached genome-wide significance included three modestly correlated variants, at 15q25.1 within PSMA4, CHRNA5 and CHRNA3 for smoking quantity, which are associated with a second signal previously reported in studies in European ancestry populations, and a signal represented by three SNPs in the SPOCK2 gene on chr10q22.1. The association at 15q25.1 confirms this region as an important susceptibility locus for smoking quantity in men and women of African ancestry. Larger studies will be needed to validate the suggestive loci that did not reach genome-wide significance and further elucidate the contribution of genetic variation to disparities in cigarette consumption, SC and smoking-attributable disease between African Americans and European Americans.
吸烟行为的遗传基因座的鉴定和探索主要在欧洲血统的人群中进行。在这里,我们报告了少数族裔人群烟草研究遗传学联盟(n = 32389)中非洲裔美国人吸烟行为的全基因组关联研究荟萃分析的结果。我们在染色体 15q25.1 上发现了一个与吸烟量(每天香烟数)相关的非编码单核苷酸多态性(SNP;rs2036527[A]),这超过了全基因组显著性(β = 0.040,s.e. = 0.007,P = 1.84×10(-8))。该变体存在于 CHRNA5 基因的 5'-远端增强子区域,是在欧洲血统研究中报告的主要索引信号。没有其他 SNP 达到吸烟起始(SI,是否曾吸烟)、SI 年龄或戒烟(SC,是否曾吸烟)的全基因组显著性。接近全基因组显著性的信息关联包括三个适度相关的变体,在 15q25.1 内的 PSMA4、CHRNA5 和 CHRNA3 与吸烟量相关,这与以前在欧洲血统人群研究中报告的第二个信号相关,以及一个由 chr10q22.1 上三个 SNP 代表的信号。15q25.1 的关联证实了该区域是非洲裔美国男性和女性吸烟量的重要易感基因座。需要更大的研究来验证未达到全基因组显著性的提示性基因座,并进一步阐明遗传变异对非洲裔美国人和欧洲裔美国人之间香烟消费、SC 和与吸烟相关疾病差异的贡献。