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

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.

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International journal of environmental research and public health

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