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氧化应激相关基因变异可能会改变邻苯二甲酸酯暴露与哮喘之间的关联。

Oxidative Stress-Related Genetic Variants May Modify Associations of Phthalate Exposures with Asthma.

作者信息

Wang I-Jen, Karmaus Wilfried J J

机构信息

Department of Pediatrics, Taipei Hospital, Ministry of Health and Welfare, Taipei 11267, Taiwan.

Institute of Environmental & Occupational Health Sciences, School of Medicine, National Yang-Ming University, Taipei 100044, Taiwan.

出版信息

Int J Environ Res Public Health. 2017 Feb 8;14(2):162. doi: 10.3390/ijerph14020162.

Abstract

Phthalate exposure may increase the risk of asthma. Little is known about whether oxidative-stress related genes may alter this association. First, this motivated us to investigate whether genetic polymorphisms of the oxidative-stress related genes glutathione -transferase Mu 1 (), glutathione -transferase pi 1 (), superoxide dismutase 2 (), catalase (), myeloperoxidase (), and In a case-control study composed of 126 asthmatic children and 327 controls, urine phthalate metabolites (monoethyl phthalate (MEP), monobutyl phthalate (MBP), monobenzyl phthalate (MBzP), and mono(2-ethyl-5-hydroxyhexyl)phthalate (MEHHP) were measured by UPLC-MS/MS at age 3. Genetic variants were analyzed by TaqMan assay. Information on asthma and environmental exposures was also collected. Analyses of variance and logistic regressions were performed. Urine MEHHP levels were associated with asthma (adjusted OR 1.33, 95% CI (1.11-1.60). Children with the (rs1695) AA and (rs5746136) TT genotypes had higher MEHHP levels as compared to GG and CC types, respectively. Since only TT genotype was significantly associated with asthma (adjusted OR (95% CI): 2.78 (1.54-5.02)), we estimated whether variants modify the association of MEHHP levels and asthma. As MEHHP concentrations were dependent on and , but the assessment of interaction requires independent variables, we estimated MEHHP residuals and assessed their interaction, showing that the OR for TT was further elevated to 3.32 (1.75-6.32) when the residuals of MEHHP were high. Urine phthalate metabolite concentrations are associated with oxidative-stress related genetic variants. Genetic variants of , considered to be reflect oxidative stress metabolisms, might modify the association of phthalate exposure with asthma.

摘要

邻苯二甲酸盐暴露可能会增加患哮喘的风险。关于氧化应激相关基因是否会改变这种关联,我们知之甚少。首先,这促使我们研究氧化应激相关基因谷胱甘肽 - 转移酶 Mu 1()、谷胱甘肽 - 转移酶 pi 1()、超氧化物歧化酶 2()、过氧化氢酶()、髓过氧化物酶()以及 的基因多态性。在一项由 126 名哮喘儿童和 327 名对照组成的病例对照研究中,在 3 岁时通过超高效液相色谱 - 串联质谱法(UPLC - MS/MS)测量尿邻苯二甲酸酯代谢物(单乙基邻苯二甲酸酯(MEP)、单丁基邻苯二甲酸酯(MBP)、单苄基邻苯二甲酸酯(MBzP)和单(2 - 乙基 - 5 - 羟基己基)邻苯二甲酸酯(MEHHP))。通过 TaqMan 分析测定基因变异。还收集了有关哮喘和环境暴露的信息。进行了方差分析和逻辑回归。尿 MEHHP 水平与哮喘相关(调整后的比值比为 1.33,95%可信区间(1.11 - 1.60))。与 GG 和 CC 类型相比,携带 (rs1695)AA 和 (rs5746136)TT 基因型的儿童 MEHHP 水平更高。由于只有 TT 基因型与哮喘显著相关(调整后的比值比(95%可信区间):2.78(1.54 - 5.02)),我们估计 变异是否会改变 MEHHP 水平与哮喘之间的关联。由于 MEHHP 浓度依赖于 和 ,但相互作用的评估需要自变量,我们估计了 MEHHP 残差并评估了它们的相互作用,结果表明当 MEHHP 残差较高时,TT 的比值比进一步升高至 3.32(1.75 - 6.32)。尿邻苯二甲酸酯代谢物浓度与氧化应激相关基因变异有关。被认为反映氧化应激代谢的 的基因变异可能会改变邻苯二甲酸盐暴露与哮喘之间的关联。

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