4.6 Article

Independent and combined effects of exposure to organophosphate esters on thyroid hormones in children and adolescents

Journal

ENVIRONMENTAL GEOCHEMISTRY AND HEALTH
Volume 45, Issue 6, Pages 3833-3846

Publisher

SPRINGER
DOI: 10.1007/s10653-022-01464-w

Keywords

Organophosphate esters; Thyroid hormones; Children and adolescents; Urine; Quantile g-computation

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This study conducted in Liuzhou, China, involved 1156 children and adolescents aged 6-18 years. The findings suggest that exposure to organophosphate esters (OPEs) may have adverse effects on thyroid function, especially in children and adolescents. The study also found that OPE exposure was associated with increased levels of triiodothyronine (T3) and free triiodothyronine (FT3) in males, and decreased levels of free thyroxine (FT4) in females.
Toxicological studies suggest that organophosphate esters (OPEs) may impair thyroid function. Epidemiological evidence, related to children and adolescents, has not been reported, and little is known about the combined effects of exposure to OPE mixtures. In this study, we collected information of 1156 children and adolescents (aged 6-18 years, 48.4% males) from a cross-sectional study in Liuzhou, China, and measured the levels of 15 urinary OPE metabolites and 5 serum thyroid hormones. Multivariate linear regression and quantile g-computation (QGC) approach were used to examine the associations which adjusted for demographic and lifestyle characteristics. Few participants had levels of triiodothyronine (T3) and free thyroxine (FT4) outside age-specific pediatric ranges. QGC analyses showed that individuals in the second, third, and fourth quartiles (Q2-Q4) of exposure had 3.93% (2.14%, 5.75%), 8.01% (4.32%, 11.8%), and 12.3% (6.54%, 18.3%) higher T3 than those in the first quartile (Q1), with similar pattern for free triiodothyronine (FT3). Individuals in Q2 and Q3 had higher thyroid-stimulating hormone (TSH) than those in Q1, but no differences were observed in TSH between Q1-Q4. In contrast, compared to the lowest quartile, FT4 was lower for those in Q2 (- 1.54%; 95% CI: -3.02%, -0.04%), Q3 (-3.07%; 95% CI: -5.95%, -0.09%), and Q4 (-4.56%; 95% CI: - 8.80%, -0.13%). These associations were consistent with the results from multivariate linear regression. When stratified by sex, OPE exposure (individual or mixtures) was associated with increased T3 and FT3 in males and decreased FT4 in females. This study provides the first evidence to characterize the thyroid-disrupting effects of OPE exposure in children and adolescents.

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