4.8 Article

Associations of Urinary Phthalate Metabolites with Thyroid Function and the Mediated Role of Cytokines: A Panel Study of Healthy Children

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AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c07656

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phthalates; thyroid function; cytokines; BKMR; mediation effects

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This study aimed to explore the associations of 10 urinary phthalate metabolites with thyroid function indicators among children. The results showed significant positive relationships between certain phthalate metabolites and thyroid-stimulating hormone or free thyroxine levels. Additionally, a mixture of these phthalate metabolites was found to be associated with elevated thyroid-stimulating hormone and free thyroxine levels, with mono-(2-ethylhexyl) phthalate and monobenzyl phthalate being major contributors. The study also identified IL-16 as a mediator of the relationships between certain phthalate metabolites and thyroid-stimulating hormone levels.
Evidence on joint association of a phthalate mixture with thyroid function among children and its underlying mechanism is largely unknown. We aimed to explore the associations of 10 urinary phthalate metabolites (mPAEs), either as individuals or as a mixture, with thyroid function indicators [free thyroxine, free triiodothyronine (FT3), and thyroid-stimulating hormone (TSH)] in 144 children aged 4-12 years with up to 3 repeated visits across 3 seasons. Significant and positive associations were observed for mono-(2-ethylhexyl) phthalate (MEHP), mono-iso-butyl phthalate (MiBP), and mono-n-butyl phthalate (MnBP) with TSH, as well as monobenzyl phthalate (MBzP) with FT3 in dose-response manners. The relationship between MEHP and TSH remained robust in multiple-phthalate models. Bayesian kernel machine regression (BKMR) models revealed overall linear associations of the 10 mPAE mixture with higher TSH and FT3 levels, and MEHP and MBzP were major contributors. Meanwhile, MEHP, MiBP, and MnBP were linked to the elevation of multiple cytokines including CCL 27, CCL3, CXCL1, and IL-16. Among them, IL-16 mediated the relationships of MEHP and MiBP with TSH, and the mediated proportions were 24.16% and 24.27%, respectively. Our findings suggested that mPAEs dominated by MEHP were dose-responsively associated with elevated TSH among healthy children and mediated by IL-16.

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