Zavras Athanasios I, Wu Tianxia, Laskaris George, Wang Yue-Fen, Cartsos Vassiliki, Segas John, Lefantzis Dimitris, Joshipura Kaumudi, Douglass Chester W, Diehl Scott R
Department of Oral Health Policy and Epidemiology, Harvard School of Dental Medicine, Boston, MA, USA.
Int J Cancer. 2002 Feb 1;97(4):526-30. doi: 10.1002/ijc.1642.
We investigated effects on oral cancer (OC) risk of an interaction between a single nucleotide polymorphism (SNP) in the alcohol dehydrogenase 3 (ADH3) gene and alcohol consumption levels using a hospital-based study of 93 cases and 99 controls conducted in Athens, Greece. This SNP affects ethanol metabolism in vitro and appeared to interact with alcohol consumption in a previous OC study. We also evaluated a SNP in CYP2E1, another gene involved in ethanol metabolism, reported to be associated with OC risk in a European population. Data on genotypes and risk factors obtained from interviews were analyzed using multivariate logistic regression, accounting for potential confounders. No overall (marginal) association was found between OC risk and ADH3 genotypes. An interaction between ADH3 genotypes and alcohol consumption levels, however, was suggested. In non-drinkers, the ADH3(1-1) genotype has higher risk than ADH3(1-2) or ADH3(2-2) genotypes, but for subjects consuming alcohol, lower risk was observed for ADH3. We fit a logistic regression model to estimate the increase in OC risk associated with each alcohol drink consumed per week. We estimated that OC risk increased by 31.5% per drink/week for the ADH3(2-2) genotype, 4.1% for the ADH3(1-2) genotype and 1.6% for the ADH3(1-1) genotype. Evidence of genotype-environment interaction was suggestive (p = 0.048, Wald chi p = 0.145, likelihood ratio). This finding is opposite to that reported for a population in Puerto Rico, where the ADH3(1-1) genotype seemed more sensitive to ethanol exposure. In Greece, genetic variation at the CYP2E1 SNP is almost entirely absent, with only 1 case and 1 control heterozygous for the variant. By contrast, in a population in France where an OC association was reported, the frequency of CYP2E1 heterozygotes was 5% in controls and 9% in OC cases. These findings illustrate the importance of replicating SNP associations both within and between different racial and ethnic groups and geographic regions.
我们在希腊雅典开展了一项基于医院的研究,纳入93例口腔癌(OC)病例和99例对照,调查了酒精脱氢酶3(ADH3)基因中的单核苷酸多态性(SNP)与饮酒水平之间的相互作用对口腔癌风险的影响。该SNP在体外影响乙醇代谢,且在之前一项口腔癌研究中似乎与饮酒存在相互作用。我们还评估了CYP2E1基因中的一个SNP,CYP2E1是另一个参与乙醇代谢的基因,据报道在欧洲人群中与口腔癌风险相关。通过多因素逻辑回归分析了从访谈中获得的基因型和风险因素数据,并对潜在混杂因素进行了校正。未发现口腔癌风险与ADH3基因型之间存在总体(边缘)关联。然而,提示ADH3基因型与饮酒水平之间存在相互作用。在不饮酒者中,ADH3(1 - 1)基因型的风险高于ADH3(1 - 2)或ADH3(2 - 2)基因型,但对于饮酒者,ADH3的风险较低。我们拟合了一个逻辑回归模型来估计每周每多饮用一杯酒相关的口腔癌风险增加情况。我们估计,对于ADH3(2 - 2)基因型,每杯酒/周使口腔癌风险增加31.5%,对于ADH3(1 - 2)基因型增加4.1%,对于ADH3(1 - 1)基因型增加1.6%。基因型 - 环境相互作用的证据具有提示性(p = 0.048,Wald卡方检验p = 0.145,似然比检验)。这一发现与波多黎各人群的报道相反,在波多黎各,ADH3(1 - 1)基因型似乎对乙醇暴露更敏感。在希腊,CYP2E1 SNP几乎完全不存在基因变异,只有1例病例和1例对照为该变异的杂合子。相比之下,在法国一个报道了口腔癌关联的人群中,CYP2E1杂合子在对照中的频率为5%,在口腔癌病例中为9%。这些发现说明了在不同种族和民族群体以及地理区域内和之间重复SNP关联研究的重要性。