Zhang Chan, Ding Heng, Cheng Yujing, Chen Wanlu, Li Qi, Li Qing, Dai Run, Luo Manlin
Department of Blood Transfusion, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming 650032, Yunnan, China.
Honghe Center Blood Station, Mengzi 661100, Yunnan, China.
Oncotarget. 2017 Jan 31;8(5):8597-8603. doi: 10.18632/oncotarget.14354.
We investigated the association between single nucleotide polymorphisms (SNPs) in ALDH2, which has been associated with alcohol dependence and several types of diseases, and the risk of drug addiction in a Chinese Han population. In a case-control study that included 692 cases and 700 healthy controls, eight SNPs in ALDH2 were selected and genotyped using the Sequenom MassARRAY platform. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using unconditional logistic regression after adjusting for age and gender. We determined that rs671 is significantly associated with a 1.551-fold increased drug addiction risk (95% CI = 1.263-1.903; p < 0.001). In the genetic model analysis, we found that rs671 is associated with an increased risk of drug addiction under additive, dominant and recessive models (p < 0.001), while rs886205, rs441 and rs4646778 displayed a decreased drug addiction risk under additive and recessive model, respectively (p < 0.05). SNP rs671 remained significant after Bonferroni correction (p<0.00125). Additionally, we observed that haplotype "GTCAC" was associated with increased drug addiction risk (OR = 1.668; 95% CI, 1.328-2.094, p < 0.001); in contrast, "ATCGC" was a protective haplotype for drug addiction risk (OR = 0.444; 95% CI, 0.281-0.704, p < 0.001). Our findings showed that ALDH2 polymorphisms are significantly associated with the risk of drug addiction in the Chinese Han population.
我们研究了与酒精依赖及多种疾病相关的乙醛脱氢酶2(ALDH2)单核苷酸多态性(SNP)与中国汉族人群药物成瘾风险之间的关联。在一项包含692例病例和700名健康对照的病例对照研究中,选取了ALDH2基因中的8个SNP,并使用Sequenom MassARRAY平台进行基因分型。在对年龄和性别进行校正后,采用非条件逻辑回归计算比值比(OR)和95%置信区间(CI)。我们确定rs671与药物成瘾风险显著增加相关,风险增加1.551倍(95%CI = 1.263 - 1.903;p < 0.001)。在遗传模型分析中,我们发现rs671在加性、显性和隐性模型下均与药物成瘾风险增加相关(p < 0.001),而rs886205、rs441和rs4646778在加性和隐性模型下分别显示出药物成瘾风险降低(p < 0.05)。经Bonferroni校正后,SNP rs671仍具有显著性(p<0.00125)。此外,我们观察到单倍型“GTCAC”与药物成瘾风险增加相关(OR = 1.668;95%CI,1.328 - 2.094,p < 0.001);相反,“ATCGC”是药物成瘾风险的保护性单倍型(OR = 0.444;95%CI,0.281 - 0.704,p < 0.001)。我们的研究结果表明,ALDH2基因多态性与中国汉族人群的药物成瘾风险显著相关。