4.7 Article

The associations between prenatal exposure to polycyclic aromatic hydrocarbon metabolites, umbilical cord blood mitochondrial DNA copy number, and children's neurobehavioral development

Journal

ENVIRONMENTAL POLLUTION
Volume 265, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2020.114594

Keywords

polycyclic aromatic hydrocarbons; Prenatal exposure; Children's neurobehavioral development; Mitochondrial DNA copy Number; Mediation effect

Funding

  1. National Natural Science Foundation of China [81673143, 81072279, 30800899]
  2. Shanxi Province Natural Science Foundation of China [2015011128, 2010021034-3]
  3. Shanxi Scholarship Council of China [2016057]
  4. Schmidt Family Foundation [G-1610-56442]
  5. Rockefeller Brothers Foundation [17e101]

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Exposure to polycyclic aromatic hydrocarbons (PAHs) during pregnancy is a risk factor for adverse neurobehavioral development outcomes. Mitochondrial DNA are sensitive to environmental toxicants due to the limited ability of repairing. The change of mitochondrial DNA copy number (mtDNAcn) might be a biologically mechanism linking PAH exposure and children's neurobehavioral impairment. Our aims are to explore whether PAH metabolites in maternal urine were associated with children's neurobehavioral development at 2 years old and umbilical cord blood mtDNAcn, and whether mtDNAcn was a mediator of PAH-related neurobehavioral development. We included 158 non-smoking pregnant women from Taiyuan City, Shanxi Province. Maternal urinary eleven PAH metabolites were detected by high performance liquid chromatography with tandem mass spectrometry (HPLC-MS/MS). MtDNAcn in cord blood was detected by real time quantitative polymerase chain reaction (RT-PCR). Children's neurodevelopment was measured by Gesell Developmental Schedules (GDS) when children were two years age. Generalized linear models and restricted cubic spline models were applied to assess the relationships between PAH metabolites in maternal urine and GDS scores and mtDNAcn. A mediation analysis was also conducted. Generalized linear models showed the relationships of sum of PAH metabolites (Sigma-OHPAHs) in maternal urine with decreased motor score, and Sigma-OHPAHs with increased mtDNAcn (p for trend < 0.05). Urinary levels of Ln (Sigma-OHPAHs) increased one unit was related to a 2.08 decreased in motor scores, and Ln (Sigma-OHPAHs) increased one unit was related to 0.15 increased in mtDNAcn. Mediation analysis did not find mtDNAcn can be a mediator between PAH metabolites and neurobehavioral development. Our results suggest that prenatal exposure to PAH decreased children's neurobehavioral development scores and increased mtDNAcn. And reducing exposure to PAH during pregnancy will benefit to improving neurobehavioral development in children. In our present cohort study, sum of PAH metabolites in urine of pregnant women were related with motor score and were positively associated with umbilical cord blood mtDNA copy number. (C) 2020 Elsevier Ltd. All rights reserved.

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