Direct LC-MS/MS and indirect GC-MS/MS methods for measuring urinary bisphenol A concentrations are comparable.


Journal

Environment international
ISSN: 1873-6750
Titre abrégé: Environ Int
Pays: Netherlands
ID NLM: 7807270

Informations de publication

Date de publication:
12 2021
Historique:
received: 27 05 2021
revised: 17 08 2021
accepted: 08 09 2021
pubmed: 20 9 2021
medline: 21 10 2021
entrez: 19 9 2021
Statut: ppublish

Résumé

Bisphenol A (BPA) is typically measured in urine using an indirect method that involves enzymatic deconjugation and extraction. In contrast, the direct method measures free and conjugated BPA concurrently and sums them to estimate urinary BPA concentrations. Statistical comparison of total BPA results using the direct and indirect methods is necessary to accurately interpret biomonitoring data for risk assessments. To compare urinary BPA concentrations estimated from the indirect and direct methods in duplicate first trimester urine samples collected from 1879 pregnant women from the MIREC Study. For the indirect method, we measured urinary BPA concentrations using GC-MS/MS. For the direct method, we summed free and conjugated BPA concentrations measured using LC-MS/MS. We evaluated deviation between the two methods using the Bland-Altman analysis in the total sample and stratified (1) by specific gravity and (2) at the limit of quantification (LOQ). Median urinary BPA concentrations for the direct and indirect methods were 0.89 µg BPA equivalents/L and 0.81 µg/L respectively. Concentrations from the direct method were, on average, 8.6% (95% CI: 6.7%, 10.5%) higher than the indirect method in a Bland-Altman analysis. The percent differences between the two methods was 4.0% in urines with specific gravities < 1.02 (n = 1348, 72%) and 20.3% in urine with specific gravity ≥ 1.02. In values below the LOQ (n = 663, 35%), we observed smaller average percent deviation (4.8%) between the two methods but wider limits of agreement. Results from this study, based on the largest statistically rigorous comparison of the direct and indirect methods of BPA measurement, contrast previous findings reporting that the indirect method underestimates total BPA exposure. The difference in urinary BPA concentrations we observed with the indirect and direct methods is unlikely to alter the interpretation of health outcome data.

Sections du résumé

BACKGROUND
Bisphenol A (BPA) is typically measured in urine using an indirect method that involves enzymatic deconjugation and extraction. In contrast, the direct method measures free and conjugated BPA concurrently and sums them to estimate urinary BPA concentrations. Statistical comparison of total BPA results using the direct and indirect methods is necessary to accurately interpret biomonitoring data for risk assessments.
OBJECTIVES
To compare urinary BPA concentrations estimated from the indirect and direct methods in duplicate first trimester urine samples collected from 1879 pregnant women from the MIREC Study.
METHODS
For the indirect method, we measured urinary BPA concentrations using GC-MS/MS. For the direct method, we summed free and conjugated BPA concentrations measured using LC-MS/MS. We evaluated deviation between the two methods using the Bland-Altman analysis in the total sample and stratified (1) by specific gravity and (2) at the limit of quantification (LOQ).
RESULTS
Median urinary BPA concentrations for the direct and indirect methods were 0.89 µg BPA equivalents/L and 0.81 µg/L respectively. Concentrations from the direct method were, on average, 8.6% (95% CI: 6.7%, 10.5%) higher than the indirect method in a Bland-Altman analysis. The percent differences between the two methods was 4.0% in urines with specific gravities < 1.02 (n = 1348, 72%) and 20.3% in urine with specific gravity ≥ 1.02. In values below the LOQ (n = 663, 35%), we observed smaller average percent deviation (4.8%) between the two methods but wider limits of agreement.
DISCUSSION
Results from this study, based on the largest statistically rigorous comparison of the direct and indirect methods of BPA measurement, contrast previous findings reporting that the indirect method underestimates total BPA exposure. The difference in urinary BPA concentrations we observed with the indirect and direct methods is unlikely to alter the interpretation of health outcome data.

Identifiants

pubmed: 34537522
pii: S0160-4120(21)00499-2
doi: 10.1016/j.envint.2021.106874
pmc: PMC8801255
mid: NIHMS1742237
pii:
doi:

Substances chimiques

Benzhydryl Compounds 0
Phenols 0
bisphenol A MLT3645I99

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106874

Subventions

Organisme : NICHD NIH HHS
ID : HHSN267200700023C
Pays : United States
Organisme : CIHR
ID : MOP-81285
Pays : Canada

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

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Auteurs

Jillian Ashley-Martin (J)

Environmental Health Science and Research Bureau, Healthy Environments and Consumer Branch, Health Canada, Canada. Electronic address: jillian.ashley-martin@canada.ca.

Éric Gaudreau (É)

Centre de Toxicologie du Québec (CTQ), Institut national de santé publique du Québec (INSPQ), Québec, Canada. Electronic address: eric.gaudreau@inspq.qc.ca.

Pierre Dumas (P)

Centre de Toxicologie du Québec (CTQ), Institut national de santé publique du Québec (INSPQ), Québec, Canada. Electronic address: pierre.dumas@inspq.qc.ca.

Chun Lei Liang (CL)

Environmental Health Science and Research Bureau, Healthy Environments and Consumer Branch, Health Canada, Canada. Electronic address: chunlei.liang@canada.ca.

Agata Logvin (A)

Environmental Health Science and Research Bureau, Healthy Environments and Consumer Branch, Health Canada, Canada. Electronic address: agata.logvin@canada.ca.

Patrick Bélanger (P)

Centre de Toxicologie du Québec (CTQ), Institut national de santé publique du Québec (INSPQ), Québec, Canada. Electronic address: patrick.belanger@inspq.qc.ca.

Gilles Provencher (G)

Centre de Toxicologie du Québec (CTQ), Institut national de santé publique du Québec (INSPQ), Québec, Canada. Electronic address: gilles.provencher@inspq.qc.ca.

Sebastien Gagne (S)

Centre de Toxicologie du Québec (CTQ), Institut national de santé publique du Québec (INSPQ), Québec, Canada. Electronic address: sebastien.gagne@inspq.qc.ca.

Warren Foster (W)

Department of Obstetrics & Gynaecology and School of Biomedical Engineering, McMaster University, Canada. Electronic address: fosterw@mcmaster.ca.

Bruce Lanphear (B)

Faculty of Health Sciences, Simon Fraser University, Canada. Electronic address: bruce_lanphear@sfu.ca.

Tye E Arbuckle (TE)

Environmental Health Science and Research Bureau, Healthy Environments and Consumer Branch, Health Canada, Canada. Electronic address: tye.arbuckle@canada.ca.

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