AI Article Synopsis

  • This study investigated the link between prenatal exposure to per- and polyfluoroalkyl substances (PFAS) and autism-related traits in children using data from 1,429 participants across 10 cohorts in the NIH-funded ECHO program.
  • The analysis showed that most PFAS in maternal blood had no significant association with child autism traits, but higher levels of perfluorononanoic acid (PFNA) were linked to increased autism-related traits.
  • The findings suggest a potential connection between PFNA levels during pregnancy and modest increases in autism traits, indicating the need for further research on various PFAS and their impacts on child development.

Article Abstract

Background: Epidemiologic evidence linking prenatal exposure to per- and polyfluoroalkyl substances (PFAS) with altered neurodevelopment is inconclusive, and few large studies have focused on autism-related outcomes. We investigated whether blood concentrations of PFAS in pregnancy are associated with child autism-related outcomes.

Methods: We included 10 cohorts from the National Institutes of Health (NIH)-funded Environmental influences on Child Health Outcomes (ECHO) program (n = 1,429). We measured 14 PFAS analytes in maternal blood collected during pregnancy; eight analytes met detection criteria for analysis. We assessed quantitative autism-related traits in children via parent report on the Social Responsiveness Scale (SRS). In multivariable linear models, we examined relationships of each PFAS (natural log-transformed) with SRS scores. We further modeled PFAS as a complex mixture using Bayesian methods and examined modification of these relationships by child sex.

Results: Most PFAS in maternal blood were not associated with child SRS T-scores. Perfluorononanoic acid (PFNA) showed the strongest and most consistent association: each 1-unit increase in ln-transformed PFNA was associated with greater autism-related traits (adjusted β [95% confidence interval (CI)] = 1.5 [-0.1, 3.0]). The summed mixture, which included six PFAS detected in >70% of participants, was not associated with SRS T-scores (adjusted β [95% highest posterior density interval] = 0.7 [-1.4, 3.0]). We did not observe consistent evidence of sex differences.

Conclusions: Prenatal blood concentrations of PFNA may be associated with modest increases in child autism-related traits. Future work should continue to examine the relationship between exposures to both legacy and emerging PFAS and additional dimensional, quantitative measures of childhood autism-related outcomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074577PMC
http://dx.doi.org/10.1097/EDE.0000000000001587DOI Listing

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