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Interaction between Arsenic Exposure from Drinking Water and Genetic Polymorphisms on Cardiovascular Disease in Bangladesh: A Prospective Case-Cohort Study

机译:孟加拉国饮用水中砷暴露与遗传多态性之间的相互作用:前瞻性病例队列研究

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Background: Epidemiologic data on genetic susceptibility to cardiovascular effects of arsenic exposure from drinking water are limited.Objective: We investigated whether the association between well-water arsenic and cardiovascular disease (CVD) differed by 170 single nucleotide polymorphisms (SNPs) in 17 genes related to arsenic metabolism, oxidative stress, inflammation, and endothelial dysfunction.Method: We conducted a prospective case-cohort study nested in the Health Effects of Arsenic Longitudinal Study, with a random subcohort of 1,375 subjects and 447 incident fatal and nonfatal cases of CVD. Well-water arsenic was measured in 2000 at baseline. The CVD cases, 56 of which occurred in the subcohort, included 238 coronary heart disease cases, 165 stroke cases, and 44 deaths due to other CVD identified during follow-up from 2000 to 2012.Results: Of the 170 SNPs tested, multiplicative interactions between well-water arsenic and two SNPs, rs281432 in ICAM1 (padj = 0.0002) and rs3176867 in VCAM1 (padj = 0.035), were significant for CVD after adjustment for multiple testing. Compared with those with GC or CC genotype in rs281432 and lower well-water arsenic, the adjusted hazard ratio (aHR) for CVD was 1.82 (95% CI: 1.31, 2.54) for a 1-SD increase in well-water arsenic combined with the GG genotype, which was greater than expected given aHRs of 1.08 and 0.96 for separate effects of arsenic and the genotype alone, respectively. Similarly, the joint aHR for arsenic and the rs3176867 CC genotype was 1.34 (95% CI: 0.95, 1.87), greater than expected given aHRs for their separate effects of 1.02 and 0.84, respectively.Conclusions: Associations between CVD and arsenic exposure may be modified by genetic variants related to endothelial dysfunction.Citation: Wu F, Jasmine F, Kibriya MG, Liu M, Cheng X, Parvez F, Islam T, Ahmed A, Rakibuz-Zaman M, Jiang J, Roy S, Paul-Brutus R, Slavkovich V, Islam T, Levy D, VanderWeele TJ, Pierce BL, Graziano JH, Ahsan H, Chen Y. 2015. Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study. Environ Health Perspect 123:451–457; 
机译:背景:关于饮用水中砷暴露对心血管疾病的遗传易感性的流行病学数据是有限的。方法:我们进行了一项前瞻性病例队列研究,该研究嵌套在砷纵向研究的健康影响中,随机分组了1,375名受试者和447例致命和非致命的CVD病例。 2000年在基线时测量了井水砷。在2000年至2012年的随访期间,CVD病例中有56例发生在亚人群中,包括238例冠心病病例,165例中风病例和44例因其他CVD导致的死亡。结果:在所测试的170个SNP中,存在乘法相互作用在井水砷和两个SNP之间,ICAM1中的rs281432(padj = 0.0002)和VCAM1中的rs3176867(padj = 0.035),经过多次测试调整后对于CVD而言意义重大。与rs281432中具有GC或CC基因型且井水砷含量较低的那些相比,由于井水砷与1-SD的增加相结合,CVD的调整后的危险比(aHR)为1.82(95%CI:1.31,2.54) GG基因型,分别比砷和单独基因型单独作用的aHR为1.08和0.96时要高出预期。同样,砷和rs3176867 CC基因型的联合aHR为1.34(95%CI:0.95,1.87),高于预期的aHR分别具有1.02和0.84的独立作用。结论:CVD和砷暴露之间的关联可能是被与内皮功能障碍有关的遗传变异修饰。引文:Wu F,Jasmine F,Kibriya MG,Liu M,Cheng X,Parvez F,Islam T,Ahmed A,Rakibuz-Zaman M,Jiang J,Roy S,Paul-Brutus R ,Slavkovich V,伊斯兰教T,利维D,范德韦勒TJ,皮尔斯BL,格拉齐亚诺·JH,阿桑·H,陈Chen。2015年。孟加拉国饮用水中砷暴露与遗传多态性之间的相互作用:一项前瞻性病例队列研究。环境健康透视123:451–457;

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