Prenatal Exposure to Per- and Polyfluoroalkyl Substances and Childhood Autism-related Outcomes

Author:

Ames Jennifer L.1ORCID,Burjak Mohamad2,Avalos Lyndsay A.1,Braun Joseph M.3,Bulka Catherine M.4,Croen Lisa A.1,Dunlop Anne L.5,Ferrara Assiamira1,Fry Rebecca C.6,Hedderson Monique M.1,Karagas Margaret R.7,Liang Donghai8,Lin Pi-I D.9,Lyall Kristen10,Moore Brianna11,Morello-Frosch Rachel12,O’Connor Thomas G.13,Oh Jiwon14,Padula Amy M.15,Woodruff Tracey J.15,Zhu Yeyi1,Hamra Ghassan B.2,

Affiliation:

1. Division of Research, Kaiser Permanente Northern California, Oakland, CA

2. John Hopkins University, Baltimore, MD

3. Department of Epidemiology, Brown University, Providence, RI

4. College of Public Health, University of South Florida, Tampa, FL

5. Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA

6. Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC

7. Geisel School of Medicine at Dartmouth, Hanover, NH

8. Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA

9. Division of Chronic Disease Research Across the Lifecourse (CoRAL), Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, MA

10. A.J. Drexel Autism Institute, Drexel University, Philadelphia, PA

11. Department of Epidemiology, Colorado School of Public Health, University of Colorado, Anschutz Medical Campus, Aurora, CO

12. School of Public Health, University of California, Berkeley, CA

13. Department of Psychiatry, University of Rochester, Rochester, NY

14. Department of Public Health Sciences, University of California, Davis, Davis CA

15. Program on Reproductive Health and the Environment, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, CA.

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Epidemiology

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