In-utero and childhood chemical exposome in six European mother-child cohorts

Harmonized data describing simultaneous exposure to a large number of environmental contaminants in-utero and during childhood is currently very limited. To characterize concentrations of a large number of environmental contaminants in pregnant women from Europe and their children, based on chemical...

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Veröffentlicht in:Environment international 2018-12, Vol.121 (Pt 1), p.751-763
Hauptverfasser: Haug, Line Småstuen, Sakhi, Amrit Kaur, Cequier, Enrique, Casas, Maribel, Maitre, Léa, Basagana, Xavier, Andrusaityte, Sandra, Chalkiadaki, Georgia, Chatzi, Leda, Coen, Muireann, de Bont, Jeroen, Dedele, Audrius, Ferrand, Joane, Grazuleviciene, Regina, Gonzalez, Juan Ramon, Gutzkow, Kristine Bjerve, Keun, Hector, McEachan, Rosie, Meltzer, Helle Margrete, Petraviciene, Inga, Robinson, Oliver, Saulnier, Pierre-Jean, Slama, Rémy, Sunyer, Jordi, Urquiza, José, Vafeiadi, Marina, Wright, John, Vrijheid, Martine, Thomsen, Cathrine
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Sprache:eng
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Zusammenfassung:Harmonized data describing simultaneous exposure to a large number of environmental contaminants in-utero and during childhood is currently very limited. To characterize concentrations of a large number of environmental contaminants in pregnant women from Europe and their children, based on chemical analysis of biological samples from mother-child pairs. We relied on the Early-Life Exposome project, HELIX, a collaborative project across six established population-based birth cohort studies in Europe. In 1301 subjects, biomarkers of exposure to 45 contaminants (i.e. organochlorine compounds, polybrominated diphenyl ethers, per- and polyfluoroalkyl substances, toxic and essential elements, phthalate metabolites, environmental phenols, organophosphate pesticide metabolites and cotinine) were measured in biological samples from children (6–12 years) and their mothers during pregnancy, using highly sensitive biomonitoring methods. Most of the exposure biomarkers had high detection frequencies in mothers (35 out of 45 biomarkers with >90% detected) and children (33 out of 45 biomarkers with >90% detected). Concentrations were significantly different between cohorts for all compounds, and were generally higher in maternal compared to children samples. For most of the persistent compounds the correlations between maternal and child concentrations were moderate to high (Spearman Rho > 0.35), while for most non-persistent compounds correlations were considerably lower (Spearman Rho 
ISSN:0160-4120
1873-6750
DOI:10.1016/j.envint.2018.09.056