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Cross-Sectional Associations between Prenatal Per- and Poly-Fluoroalkyl Substances and Bioactive Lipids in Three Environmental Influences on Child Health Outcomes (ECHO) Cohorts.
Suthar, Himal; Manea, Tomás; Pak, Dominic; Woodbury, Megan; Eick, Stephanie M; Cathey, Amber; Watkins, Deborah J; Strakovsky, Rita S; Ryva, Brad A; Pennathur, Subramaniam; Zeng, Lixia; Weller, David; Park, June-Soo; Smith, Sabrina; DeMicco, Erin; Padula, Amy; Fry, Rebecca C; Mukherjee, Bhramar; Aguiar, Andrea; Geiger, Sarah Dee; Ng, Shukhan; Huerta-Montanez, Gredia; Vélez-Vega, Carmen; Rosario, Zaira; Cordero, Jose F; Zimmerman, Emily; Woodruff, Tracey J; Morello-Frosch, Rachel; Schantz, Susan L; Meeker, John D; Alshawabkeh, Akram N; Aung, Max T.
Afiliación
  • Suthar H; Department of Population and Public Health Sciences, University of Southern California, Los Angeles, California 90032, United States.
  • Manea T; Department of Population and Public Health Sciences, University of Southern California, Los Angeles, California 90032, United States.
  • Pak D; Department of Population and Public Health Sciences, University of Southern California, Los Angeles, California 90032, United States.
  • Woodbury M; Department of Civil and Environmental Engineering, Northeastern University, Boston, Massachusetts 02115, United States.
  • Eick SM; Gangarosa Department of Environmental Health, Emory University Rollins School of Public Health, Atlanta, Georgia 30322, United States.
  • Cathey A; Department of Environmental Health Sciences, University of Michigan School of Public Health, Ann Arbor, Michigan 48109, United States.
  • Watkins DJ; Department of Environmental Health Sciences, University of Michigan School of Public Health, Ann Arbor, Michigan 48109, United States.
  • Strakovsky RS; Institute for Integrative Toxicology, Michigan State University, East Lansing, Michigan 48824, United States.
  • Ryva BA; Department of Food Sciences and Human Nutrition, Michigan State University, East Lansing, Michigan 48824, United States.
  • Pennathur S; Institute for Integrative Toxicology, Michigan State University, East Lansing, Michigan 48824, United States.
  • Zeng L; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan 48824, United States.
  • Weller D; College of Osteopathic Medicine, Michigan State University, East Lansing, Michigan 48824, United States.
  • Park JS; Department of Internal Medicine-Nephrology, University of Michigan, Ann Arbor, Michigan 48824, United States.
  • Smith S; Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • DeMicco E; Department of Internal Medicine-Nephrology, University of Michigan, Ann Arbor, Michigan 48824, United States.
  • Padula A; NSF International, Ann Arbor, Michigan 48105, United States.
  • Fry RC; Environmental Chemistry Laboratory, Department of Toxic Substances Control, California Environmental Protection Agency, Berkeley, California 94710, United States.
  • Mukherjee B; Environmental Chemistry Laboratory, Department of Toxic Substances Control, California Environmental Protection Agency, Berkeley, California 94710, United States.
  • Aguiar A; Program on Reproductive Health and the Environment, University of California, San Francisco, San Francisco, California 94143, United States.
  • Geiger SD; Program on Reproductive Health and the Environment, University of California, San Francisco, San Francisco, California 94143, United States.
  • Ng S; Department of Environmental Sciences and Engineering, University of North Carolina, Chapel Hill, Gillings School of Global Public Health, Chapel Hill, North Carolina 27599, United States.
  • Huerta-Montanez G; Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan 48109, United States.
  • Vélez-Vega C; Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign, Champaign, Illinois 61801, United States.
  • Rosario Z; Department of Comparative Biosciences, University of Illinois Urbana-Champaign, Champaign, Illinois 61802, United States.
  • Cordero JF; Department of Comparative Biosciences, University of Illinois Urbana-Champaign, Champaign, Illinois 61802, United States.
  • Zimmerman E; Department of Kinesiology and Community Health, University of Illinois at Urbana-Champaign, Champaign, Illinois 61801, United States.
  • Woodruff TJ; Department of Comparative Biosciences, University of Illinois Urbana-Champaign, Champaign, Illinois 61802, United States.
  • Morello-Frosch R; Department of Civil and Environmental Engineering, Northeastern University, Boston, Massachusetts 02115, United States.
  • Schantz SL; Department of Epidemiology and Biostatistics, University of Georgia, Athens, Georgia 30606, United States.
  • Meeker JD; University of Puerto Rico Graduate School of Public Health, San Juan, Puerto Rico 00935, United States.
  • Alshawabkeh AN; Department of Epidemiology and Biostatistics, University of Georgia, Athens, Georgia 30606, United States.
  • Aung MT; Department of Communication Sciences and Disorders, Northeastern University, Boston, Massachusetts 02115, United States.
Environ Sci Technol ; 58(19): 8264-8277, 2024 May 14.
Article en En | MEDLINE | ID: mdl-38691655
ABSTRACT
Prenatal per- and poly-fluoroalkyl substances (PFAS) exposure may influence gestational outcomes through bioactive lipids─metabolic and inflammation pathway indicators. We estimated associations between prenatal PFAS exposure and bioactive lipids, measuring 12 serum PFAS and 50 plasma bioactive lipids in 414 pregnant women (median 17.4 weeks' gestation) from three Environmental influences on Child Health Outcomes Program cohorts. Pairwise association estimates across cohorts were obtained through linear mixed models and meta-analysis, adjusting the former for false discovery rates. Associations between the PFAS mixture and bioactive lipids were estimated using quantile g-computation. Pairwise analyses revealed bioactive lipid levels associated with PFDeA, PFNA, PFOA, and PFUdA (p < 0.05) across three enzymatic pathways (cyclooxygenase, cytochrome p450, lipoxygenase) in at least one combined cohort analysis, and PFOA and PFUdA (q < 0.2) in one linear mixed model. The strongest signature revealed doubling in PFOA corresponding with PGD2 (cyclooxygenase pathway; +24.3%, 95% CI 7.3-43.9%) in the combined cohort. Mixture analysis revealed nine positive associations across all pathways with the PFAS mixture, the strongest signature indicating a quartile increase in the PFAS mixture associated with PGD2 (+34%, 95% CI 8-66%), primarily driven by PFOS. Bioactive lipids emerged as prenatal PFAS exposure biomarkers, deepening insights into PFAS' influence on pregnancy outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fluorocarburos / Lípidos Límite: Adult / Child / Female / Humans / Pregnancy Idioma: En Revista: Environ Sci Technol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fluorocarburos / Lípidos Límite: Adult / Child / Female / Humans / Pregnancy Idioma: En Revista: Environ Sci Technol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos