Associations between plasma levels of brominated flame retardants and methylation of DNA from peripheral blood: A cross-sectional study in a cohort of French women.


Journal

Environmental research
ISSN: 1096-0953
Titre abrégé: Environ Res
Pays: Netherlands
ID NLM: 0147621

Informations de publication

Date de publication:
07 2022
Historique:
received: 05 09 2021
revised: 24 12 2021
accepted: 19 01 2022
pubmed: 7 2 2022
medline: 7 5 2022
entrez: 6 2 2022
Statut: ppublish

Résumé

Brominated flame retardants (BFRs) are organic compounds that are widespread in the environment. Because of their persistence, they are able to bioaccumulate with major impacts on human health. It has been hypothesized that the effect of BFRs on human health is mediated by alterations of DNA methylation. The aim of this study was to examine the association between methylation of DNA extracted from peripheral blood and circulating levels of BFRs measured in plasma. We conducted a methylation wide association study on 336 blood samples from a study within the E3N (Etude Epidémiologique auprès de femmes de l'Education Nationale) cohort, a long-term longitudinal cohort of French women. DNA methylation at more than 850 000 cytosine-guanine dinucleotide (CpG) sites was measured with the Illumina Infinium HumanMethylation - EPIC BeadChip. Circulating levels of seven BFRs (BDE-28, BDE-47, BDE-99, BDE-100, BDE-153, BDE-154 and PBB-153) were measured by gas chromatography coupled to high-resolution mass spectrometry in plasma samples. The association between DNA methylation and BFRs plasma levels was assessed through linear mixed-effects models followed by gene-set enrichment analyses (GSEA). We identified 253 CpG sites whose methylation levels were significantly associated with exposure to BFRs after Bonferroni correction. For 50 of these CpGs the p-values were less than 2.2x10 Exposure to BFRs appears to be related to numerous alterations in DNA methylation. These findings, if replicated in independent studies, provide insights into the biological and health effects of BFRs.

Sections du résumé

BACKGROUND
Brominated flame retardants (BFRs) are organic compounds that are widespread in the environment. Because of their persistence, they are able to bioaccumulate with major impacts on human health. It has been hypothesized that the effect of BFRs on human health is mediated by alterations of DNA methylation.
OBJECTIVE
The aim of this study was to examine the association between methylation of DNA extracted from peripheral blood and circulating levels of BFRs measured in plasma.
METHODS
We conducted a methylation wide association study on 336 blood samples from a study within the E3N (Etude Epidémiologique auprès de femmes de l'Education Nationale) cohort, a long-term longitudinal cohort of French women. DNA methylation at more than 850 000 cytosine-guanine dinucleotide (CpG) sites was measured with the Illumina Infinium HumanMethylation - EPIC BeadChip. Circulating levels of seven BFRs (BDE-28, BDE-47, BDE-99, BDE-100, BDE-153, BDE-154 and PBB-153) were measured by gas chromatography coupled to high-resolution mass spectrometry in plasma samples. The association between DNA methylation and BFRs plasma levels was assessed through linear mixed-effects models followed by gene-set enrichment analyses (GSEA).
RESULTS
We identified 253 CpG sites whose methylation levels were significantly associated with exposure to BFRs after Bonferroni correction. For 50 of these CpGs the p-values were less than 2.2x10
CONCLUSIONS
Exposure to BFRs appears to be related to numerous alterations in DNA methylation. These findings, if replicated in independent studies, provide insights into the biological and health effects of BFRs.

Identifiants

pubmed: 35123963
pii: S0013-9351(22)00115-3
doi: 10.1016/j.envres.2022.112788
pii:
doi:

Substances chimiques

Flame Retardants 0
Halogenated Diphenyl Ethers 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

112788

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Hanane Omichessan (H)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, "Exposome, Heredity, Cancer and Health" Team, Gustave Roussy, Villejuif, France.

Vittorio Perduca (V)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, "Exposome, Heredity, Cancer and Health" Team, Gustave Roussy, Villejuif, France; Laboratoire MAP5 (UMR CNRS 8145), Université de Paris, Paris, France.

Silvia Polidoro (S)

Italian Institute for Genomic Medicine (IIGM), Candiolo, Italy.

Marina Kvaskoff (M)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, "Exposome, Heredity, Cancer and Health" Team, Gustave Roussy, Villejuif, France.

Thérèse Truong (T)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, "Exposome, Heredity, Cancer and Health" Team, Gustave Roussy, Villejuif, France.

German Cano-Sancho (G)

LABERCA, Oniris, INRAE, 44307, Nantes, France.

Jean-Philippe Antignac (JP)

LABERCA, Oniris, INRAE, 44307, Nantes, France.

Laura Baglietto (L)

Department of Clinical and Experimental Medicine, University of Pisa, Italy.

Francesca Romana Mancini (FR)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, "Exposome, Heredity, Cancer and Health" Team, Gustave Roussy, Villejuif, France.

Gianluca Severi (G)

Université Paris-Saclay, UVSQ, INSERM, CESP U1018, "Exposome, Heredity, Cancer and Health" Team, Gustave Roussy, Villejuif, France; Department of Statistics, Computer Science, University of Florence, Applications G. Parenti, Italy. Electronic address: gianluca.severi@inserm.fr.

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Classifications MeSH