Uhl George R, Liu Qing-Rong, Drgon Tomas, Johnson Catherine, Walther Donna, Rose Jed E
Molecular Neurobiology Branch, NIH-IRP, NIDA, Baltimore, Maryland 21224, USA.
BMC Genet. 2007 Apr 3;8:10. doi: 10.1186/1471-2156-8-10.
Classical genetic studies indicate that nicotine dependence is a substantially heritable complex disorder. Genetic vulnerabilities to nicotine dependence largely overlap with genetic vulnerabilities to dependence on other addictive substances. Successful abstinence from nicotine displays substantial heritable components as well. Some of the heritability for the ability to quit smoking appears to overlap with the genetics of nicotine dependence and some does not. We now report genome wide association studies of nicotine dependent individuals who were successful in abstaining from cigarette smoking, nicotine dependent individuals who were not successful in abstaining and ethnically-matched control subjects free from substantial lifetime use of any addictive substance.
These data, and their comparison with data that we have previously obtained from comparisons of four other substance dependent vs control samples support two main ideas: 1) Single nucleotide polymorphisms (SNPs) whose allele frequencies distinguish nicotine-dependent from control individuals identify a set of genes that overlaps significantly with the set of genes that contain markers whose allelic frequencies distinguish the four other substance dependent vs control groups (p < 0.018). 2) SNPs whose allelic frequencies distinguish successful vs unsuccessful abstainers cluster in small genomic regions in ways that are highly unlikely to be due to chance (Monte Carlo p < 0.00001).
These clustered SNPs nominate candidate genes for successful abstinence from smoking that are implicated in interesting functions: cell adhesion, enzymes, transcriptional regulators, neurotransmitters and receptors and regulation of DNA, RNA and proteins. As these observations are replicated, they will provide an increasingly-strong basis for understanding mechanisms of successful abstinence, for identifying individuals more or less likely to succeed in smoking cessation efforts and for tailoring therapies so that genotypes can help match smokers with the treatments that are most likely to benefit them.
经典遗传学研究表明,尼古丁依赖是一种遗传性很强的复杂疾病。对尼古丁依赖的遗传易感性在很大程度上与对其他成瘾物质依赖的遗传易感性重叠。成功戒除尼古丁也表现出很大的遗传成分。戒烟能力的部分遗传力似乎与尼古丁依赖的遗传学重叠,而部分则不然。我们现在报告对成功戒烟的尼古丁依赖个体、未成功戒烟的尼古丁依赖个体以及在一生中未大量使用任何成瘾物质的种族匹配对照受试者进行的全基因组关联研究。
这些数据以及它们与我们之前从其他四种物质依赖与对照样本比较中获得的数据的比较支持了两个主要观点:1)其等位基因频率区分尼古丁依赖个体与对照个体的单核苷酸多态性(SNP)识别出一组基因,该组基因与包含等位基因频率区分其他四个物质依赖与对照组的标记的基因集有显著重叠(p < 0.018)。2)其等位基因频率区分成功与未成功戒烟者的SNP以极不可能是偶然的方式聚集在小基因组区域(蒙特卡洛p < 0.00001)。
这些聚集的SNP为成功戒烟提名了候选基因,这些基因涉及有趣的功能:细胞黏附、酶、转录调节因子、神经递质和受体以及DNA、RNA和蛋白质的调节。随着这些观察结果得到重复验证,它们将为理解成功戒烟的机制、识别戒烟努力中更有可能或不太可能成功的个体以及定制疗法提供越来越坚实的基础,以便基因型能够帮助吸烟者与最可能使他们受益的治疗方法相匹配。