The association between urinary glyphosate and aminomethyl phosphonic acid with biomarkers of oxidative stress among pregnant women in the PROTECT birth cohort study.


Journal

Ecotoxicology and environmental safety
ISSN: 1090-2414
Titre abrégé: Ecotoxicol Environ Saf
Pays: Netherlands
ID NLM: 7805381

Informations de publication

Date de publication:
15 Mar 2022
Historique:
received: 15 11 2021
revised: 07 02 2022
accepted: 08 02 2022
pubmed: 15 2 2022
medline: 16 3 2022
entrez: 14 2 2022
Statut: ppublish

Résumé

Glyphosate is a widely used herbicide in global agriculture. Glyphosate and its primary environmental degradate, aminomethyl phosphonic acid (AMPA), have been shown to disrupt endocrine function and induce oxidative stress in in vitro and animal studies. To our knowledge, these relationships have not been previously characterized in epidemiological settings. Elevated urinary levels of glyphosate and AMPA may be indicative of health effects caused by previous exposure via multiple mechanisms including oxidative stress. Glyphosate and AMPA were measured in 347 urine samples collected between 16 and 20 weeks gestation and 24-28 weeks gestation from pregnant women in the PROTECT birth cohort. Urinary biomarkers of oxidative stress, comprising 8-isoprostane-prostaglandin-F2α (8-iso-PGF2α), its metabolite 2,3-dinor-5,6-dihydro-15-F No significant differences in exposure or oxidative stress biomarker concentrations were observed between study visits. An interquartile range (IQR) increase in AMPA was associated with 9.5% (95% CI: 0.5-19.3%) higher 8-iso-PGF2α metabolite concentrations. Significant linear trends were also identified when examining tertiles of exposure variables. Compared to the lowest exposure group, the second and third tertiles of AMPA were significantly associated with 12.8% (0.6-26.5%) and 15.2% (1.8-30.3%) higher 8-isoprostane metabolite, respectively. An IQR increase in glyphosate was suggestively associated with 4.7% (-0.9 to 10.7%) higher 8-iso-PGF2α. Urinary concentrations of the main environmental degradate of glyphosate, AMPA, were associated with higher levels of certain oxidative stress biomarkers. Associations with glyphosate reflected similar trends, although findings were not as strong. Additional research is required to better characterize the association between glyphosate exposure and biomarkers of oxidative stress, as well as potential downstream health consequences.

Sections du résumé

BACKGROUND BACKGROUND
Glyphosate is a widely used herbicide in global agriculture. Glyphosate and its primary environmental degradate, aminomethyl phosphonic acid (AMPA), have been shown to disrupt endocrine function and induce oxidative stress in in vitro and animal studies. To our knowledge, these relationships have not been previously characterized in epidemiological settings. Elevated urinary levels of glyphosate and AMPA may be indicative of health effects caused by previous exposure via multiple mechanisms including oxidative stress.
METHODS METHODS
Glyphosate and AMPA were measured in 347 urine samples collected between 16 and 20 weeks gestation and 24-28 weeks gestation from pregnant women in the PROTECT birth cohort. Urinary biomarkers of oxidative stress, comprising 8-isoprostane-prostaglandin-F2α (8-iso-PGF2α), its metabolite 2,3-dinor-5,6-dihydro-15-F
RESULTS RESULTS
No significant differences in exposure or oxidative stress biomarker concentrations were observed between study visits. An interquartile range (IQR) increase in AMPA was associated with 9.5% (95% CI: 0.5-19.3%) higher 8-iso-PGF2α metabolite concentrations. Significant linear trends were also identified when examining tertiles of exposure variables. Compared to the lowest exposure group, the second and third tertiles of AMPA were significantly associated with 12.8% (0.6-26.5%) and 15.2% (1.8-30.3%) higher 8-isoprostane metabolite, respectively. An IQR increase in glyphosate was suggestively associated with 4.7% (-0.9 to 10.7%) higher 8-iso-PGF2α.
CONCLUSIONS CONCLUSIONS
Urinary concentrations of the main environmental degradate of glyphosate, AMPA, were associated with higher levels of certain oxidative stress biomarkers. Associations with glyphosate reflected similar trends, although findings were not as strong. Additional research is required to better characterize the association between glyphosate exposure and biomarkers of oxidative stress, as well as potential downstream health consequences.

Identifiants

pubmed: 35158254
pii: S0147-6513(22)00140-3
doi: 10.1016/j.ecoenv.2022.113300
pmc: PMC8920761
mid: NIHMS1780063
pii:
doi:

Substances chimiques

Biomarkers 0
Phosphorous Acids 0
phosphonic acid 13598-36-2
Glycine TE7660XO1C

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113300

Subventions

Organisme : NIEHS NIH HHS
ID : P30 ES017885
Pays : United States
Organisme : NIH HHS
ID : UH3 OD023251
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES032203
Pays : United States
Organisme : NIEHS NIH HHS
ID : P42 ES017198
Pays : United States
Organisme : NIEHS NIH HHS
ID : P50 ES026049
Pays : United States

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

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Auteurs

Jarrod L Eaton (JL)

University of Michigan School of Public Health, Department of Environmental Health Sciences, Ann Arbor, MI, United States.

Amber L Cathey (AL)

University of Michigan School of Public Health, Department of Environmental Health Sciences, Ann Arbor, MI, United States.

Jennifer A Fernandez (JA)

University of Michigan School of Public Health, Department of Environmental Health Sciences, Ann Arbor, MI, United States.

Deborah J Watkins (DJ)

University of Michigan School of Public Health, Department of Environmental Health Sciences, Ann Arbor, MI, United States.

Monica K Silver (MK)

University of Michigan School of Public Health, Department of Environmental Health Sciences, Ann Arbor, MI, United States.

Ginger L Milne (GL)

Department of Medicine - Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, United States.

Carmen Velez-Vega (C)

University of Puerto Rico Graduate School of Public Health, UPR Medical Sciences Campus, San Juan, PR, United States.

Zaira Rosario (Z)

University of Puerto Rico Graduate School of Public Health, UPR Medical Sciences Campus, San Juan, PR, United States.

Jose Cordero (J)

Department of Epidemiology and Biostatistics, University of Georgia, Athens, GA, United States.

Akram Alshawabkeh (A)

College of Engineering, Northeastern University, Boston, MA, United States.

John D Meeker (JD)

University of Michigan School of Public Health, Department of Environmental Health Sciences, Ann Arbor, MI, United States. Electronic address: meekerj@umich.edu.

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Classifications MeSH