Exposure to perfluoroalkyl substances (PFAS) and association with thyroid hormones in adolescent males
Metadatos
Mostrar el registro completo del ítemAutor
Freire, Carmen; Vela Soria, Fernando; Castiello, Francesca; Salamanca Fernández, Elena; Quesada Jiménez, Raquel; López Alados, María Cristina; Fernández, Mariana F.; Olea Serrano, NicolásEditorial
Elsevier
Materia
Perfluoroalkyl substances Thyroid hormones Adolescents Endocrine disruption
Fecha
2023-07-12Referencia bibliográfica
C. Freire et al.. Exposure to perfluoroalkyl substances (PFAS) and association with thyroid hormones in adolescent males. International Journal of Hygiene and Environmental Health 252 (2023) 114219
Patrocinador
Spanish Consortium for Research on Epidemiology and Public Health (CIBERESP); Instituto de Salud Carlos III (ISCIII) (grant no. CP16/00085)Resumen
Background: Perfluoroalkyl substances (PFAS) are found in a wide range of consumer products. Exposure to PFAS
in children and adolescents may be associated with alterations in thyroid hormones, which have critical roles in
brain function.
Objective: This study investigated the association between plasma concentrations of PFAS and serum levels of
total triiodothyronine (T3), free thyroxine (T4), and thyroid-stimulating hormone (TSH) in adolescent males.
Methods: In 2017–2019, 151 boys from the Environment and Childhood (INMA)-Granada birth cohort, Spain,
participated in a clinical follow up visit at the age of 15–17 years. Plasma concentrations of ten PFAS (PFHxA,
PFHpA, PFOA, PFNA, PFDA, PFUnDA, PFDoDA, PFTrDA, PFOS, and PFHxS) and serum thyroid hormones were
measured in 129 of these boys. Linear regression analysis was performed to determine associations of individual
PFAS with total T3, free T4, TSH, and free T4/TSH ratio, and quantile g-computation models were performed to
assess the mixture effect. Additional models considered iodine status as effect modifier.
Results: PFOS was the most abundant PFAS in plasma (median = 2.22 μg/L), followed by PFOA (median = 1.00
μg/L), PFNA (median = 0.41 μg/L), and PFHxS (median = 0.40 μg/L). When adjusted by confounders (including
age, maternal schooling, and fish intake), PFOA and PFUnDA were associated with an increase in free T4 (β [95%
CI] = 0.72 [0.06; 1.38] and 0.36 [0.04; 0.68] pmol/L, respectively, per two-fold increase in plasma concentrations),
with no change in TSH. PFOS, the sum of PFOA, PFNA, PFOS, and PFHxS, and the sum of long-chain
PFAS were marginally associated with increases in free T4. Associations with higher free T4 and/or total T3 were
seen for several PFAS in boys with lower iodine intake (<108 μ/day) alone. Moreover, the PFAS mixture was
association with an increase in free T4 levels in boys with lower iodine intake (% change [95% CI] = 6.47 [–0.69;
14.11] per each quartile increase in the mixture concentration).
Conclusions: Exposure to PFAS, considered individually or as a mixture, was associated with an increase in free T4
levels in boys with lower iodine intake. However, given the small sample size, the extent of these alterations
remains uncertain