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Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort

BACKGROUND: Evidence is limited regarding the associations of prenatal and childhood per‐ and polyfluoroalkyl substance (PFAS) exposures with blood pressure (BP) trajectories in children. METHODS AND RESULTS: Participants are from Project Viva, a prospective prebirth cohort in eastern Massachusetts....

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Autores principales: Zhang, Mingyu, Aris, Izzuddin M., Lin, Pi‐I Debby, Rifas‐Shiman, Sheryl L., Brady, Tammy M., James‐Todd, Tamarra, Oken, Emily, Hivert, Marie‐France
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547341/
https://www.ncbi.nlm.nih.gov/pubmed/37642023
http://dx.doi.org/10.1161/JAHA.123.030760
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author Zhang, Mingyu
Aris, Izzuddin M.
Lin, Pi‐I Debby
Rifas‐Shiman, Sheryl L.
Brady, Tammy M.
James‐Todd, Tamarra
Oken, Emily
Hivert, Marie‐France
author_facet Zhang, Mingyu
Aris, Izzuddin M.
Lin, Pi‐I Debby
Rifas‐Shiman, Sheryl L.
Brady, Tammy M.
James‐Todd, Tamarra
Oken, Emily
Hivert, Marie‐France
author_sort Zhang, Mingyu
collection PubMed
description BACKGROUND: Evidence is limited regarding the associations of prenatal and childhood per‐ and polyfluoroalkyl substance (PFAS) exposures with blood pressure (BP) trajectories in children. METHODS AND RESULTS: Participants are from Project Viva, a prospective prebirth cohort in eastern Massachusetts. We measured PFAS in early‐pregnancy maternal (median, 9.6 weeks) and midchildhood (median, 7.7 years) plasma samples. We conducted standardized BP measurements at 6 research visits: birth, infancy (median, 6.3 months), early childhood (median, 3.2 years), midchildhood (median, 7.7 years), early adolescence (median, 12.9 years), and late adolescence (median, 17.5 years). We used linear regression to examine associations of individual PFASs with BP at each visit, linear spline mixed‐effects regression to model BP trajectories, and a mixture approach to estimate PFAS exposure burden. We included 9036 BP measures from 1506 participants. We observed associations between particular individual prenatal PFASs and child BP at specific time points, for example, prenatal 2‐(N‐ethyl‐perfluorooctane sulfonamido) acetate (EtFOSAA) and 2‐(N‐methyl‐perfluorooctane sulfonamido) acetate (MeFOSAA) with higher systolic BP at birth; prenatal perfluorooctane sulfonate (PFOS) and EtFOSAA with lower diastolic BP in infancy; and prenatal PFOS, perfluorooctanoate (PFOA), and EtFOSAA with higher systolic BP at midchildhood. No prenatal or childhood PFAS was consistently associated with BP across all visits. Diastolic BP trajectories from 0 to 20 years differed slightly by prenatal PFOA, perfluorohexane sulfonate (PFHxS), and perfluorononanoate (PFNA) (P values 0.01–0.09). Diastolic BP trajectories from 6 to 20 years differed slightly by midchildhood PFHxS and MeFOSAA (P‐values 0.03–0.08). Prenatal or childhood PFAS mixture burden scores were not associated with BP. CONCLUSIONS: We found associations of prenatal and childhood PFAS exposures with BP at specific time points between birth and late adolescence but no consistent associations across all time points or PFAS types.
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spelling pubmed-105473412023-10-04 Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort Zhang, Mingyu Aris, Izzuddin M. Lin, Pi‐I Debby Rifas‐Shiman, Sheryl L. Brady, Tammy M. James‐Todd, Tamarra Oken, Emily Hivert, Marie‐France J Am Heart Assoc Original Research BACKGROUND: Evidence is limited regarding the associations of prenatal and childhood per‐ and polyfluoroalkyl substance (PFAS) exposures with blood pressure (BP) trajectories in children. METHODS AND RESULTS: Participants are from Project Viva, a prospective prebirth cohort in eastern Massachusetts. We measured PFAS in early‐pregnancy maternal (median, 9.6 weeks) and midchildhood (median, 7.7 years) plasma samples. We conducted standardized BP measurements at 6 research visits: birth, infancy (median, 6.3 months), early childhood (median, 3.2 years), midchildhood (median, 7.7 years), early adolescence (median, 12.9 years), and late adolescence (median, 17.5 years). We used linear regression to examine associations of individual PFASs with BP at each visit, linear spline mixed‐effects regression to model BP trajectories, and a mixture approach to estimate PFAS exposure burden. We included 9036 BP measures from 1506 participants. We observed associations between particular individual prenatal PFASs and child BP at specific time points, for example, prenatal 2‐(N‐ethyl‐perfluorooctane sulfonamido) acetate (EtFOSAA) and 2‐(N‐methyl‐perfluorooctane sulfonamido) acetate (MeFOSAA) with higher systolic BP at birth; prenatal perfluorooctane sulfonate (PFOS) and EtFOSAA with lower diastolic BP in infancy; and prenatal PFOS, perfluorooctanoate (PFOA), and EtFOSAA with higher systolic BP at midchildhood. No prenatal or childhood PFAS was consistently associated with BP across all visits. Diastolic BP trajectories from 0 to 20 years differed slightly by prenatal PFOA, perfluorohexane sulfonate (PFHxS), and perfluorononanoate (PFNA) (P values 0.01–0.09). Diastolic BP trajectories from 6 to 20 years differed slightly by midchildhood PFHxS and MeFOSAA (P‐values 0.03–0.08). Prenatal or childhood PFAS mixture burden scores were not associated with BP. CONCLUSIONS: We found associations of prenatal and childhood PFAS exposures with BP at specific time points between birth and late adolescence but no consistent associations across all time points or PFAS types. John Wiley and Sons Inc. 2023-08-29 /pmc/articles/PMC10547341/ /pubmed/37642023 http://dx.doi.org/10.1161/JAHA.123.030760 Text en © 2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Zhang, Mingyu
Aris, Izzuddin M.
Lin, Pi‐I Debby
Rifas‐Shiman, Sheryl L.
Brady, Tammy M.
James‐Todd, Tamarra
Oken, Emily
Hivert, Marie‐France
Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort
title Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort
title_full Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort
title_fullStr Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort
title_full_unstemmed Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort
title_short Prenatal and Childhood Per‐ and Polyfluoroalkyl Substance (PFAS) Exposures and Blood Pressure Trajectories From Birth to Late Adolescence in a Prospective US Prebirth Cohort
title_sort prenatal and childhood per‐ and polyfluoroalkyl substance (pfas) exposures and blood pressure trajectories from birth to late adolescence in a prospective us prebirth cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547341/
https://www.ncbi.nlm.nih.gov/pubmed/37642023
http://dx.doi.org/10.1161/JAHA.123.030760
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