Disinfection By-Products and Congenital Anomalies: Evidence Still Inconclusive
نویسنده
چکیده
Infants are extremely vulnerable to certain pesticide exposures because they are still developing the ability to produce the enzyme para oxonase1 (PON1), which detoxifies certain organophosphate pesti cides such as chlorpyrifos and diazinon. A study published in 2003 indicated that children may reach nearadult levels of PON1 activ ity by age 2 years. But a new largerscale study of participants in the Center for Health Assessment in Mothers and Children of Salinas cohort has found that many children are still ramping up PON1 levels until at least age 7 and that PON1 activity can vary dramatically among children of the same age [EHP 117:1632–1638; Huen et al.]. Organophosphates have been largely banned from home use but are still widely used in agriculture. These pesticides target the nervous sys tems of insects and also affect the human nervous system. Prior work by researchers involved in the current study revealed associations between prenatal exposure to organophosphate pesticides and increased reports of developmental delays and disorders in children. Genetic variation in the PON1 gene affects the type and quantity of the enzyme produced. A singlenucleotide polymorphism at position 192 of the gene’s coding region changes the enzyme’s configuration, affecting its overall and pesticidespecific efficiency; the R allele (form) of the PON1192 polymorphism is more efficient than the Q allele at detoxi fying organophosphate metabolites. A singlenucleotide polymorphism at position –108 of the gene’s promoter region affects the amount of PON1 produced, such that persons with the C allele have higher levels of PON1 activity than persons with the T allele. In the current study, researchers measured PON1 activity from birth to age 7 years in 458 MexicanAmerican children living in a heavily agri cultural area. Blood samples were taken at up to five time points (birth, 1 year, 2 years, 5 years, and 7 years) and analyzed using three assays that measured PON1 quantity and efficiency. Blood samples were also geno typed for PON1 variations. Researchers obtained a total of 1,143 sam ples, with 108 children providing samples at four or more time points. Enzyme activity increased with age in all the children. However, compared with other children, PON1 activity was higher at birth and increased more quickly with age in children with the RR PON1192 genotype or the CC PON1–108 genotype (found in 24% and 28% of the children, respectively), such that in some cases average levels of activity against some pesticide metabolites were lower in children at age 7 than they were in other children at age 2. Children with both the RR and CC genotypes had the highest PON1 activity levels, and children with both the QQ and TT genotypes had the lowest levels. These results suggest that some children may be vulnerable to the effects of organophosphate pesticides for longer than previously thought. The authors therefore recommend that policy makers consider this new information to ensure standards for pesticide exposures adequately pro tect young children.
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