Fetal exposure to propoxur and abnormal child neurodevelopment at 2 years of age

Our aim was to determine the effects of fetal exposure to propoxur and pyrethroids, on child neurodevelopment at 2 years of age. Mothers were prospectively recruited during mid-pregnancy in Bulacan, Philippines where multiple pesticides including propoxur, cyfluthrin, chlorpyrifos, cypermethrin, pre...

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Veröffentlicht in:Neurotoxicology (Park Forest South) 2012-08, Vol.33 (4), p.669-675
Hauptverfasser: Ostrea Jr, Enrique M., Reyes, Alexis, Villanueva-Uy, Esterlita, Pacifico, Rochelle, Benitez, Bernadette, Ramos, Essie, Bernardo, Rommel C., Bielawski, Dawn M., Delaney-Black, Virginia, Chiodo, Lisa, Janisse, James J., Ager, Joel W.
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Sprache:eng
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Zusammenfassung:Our aim was to determine the effects of fetal exposure to propoxur and pyrethroids, on child neurodevelopment at 2 years of age. Mothers were prospectively recruited during mid-pregnancy in Bulacan, Philippines where multiple pesticides including propoxur, cyfluthrin, chlorpyrifos, cypermethrin, pretilachlor, bioallethrin, malathion, diazinon and transfluthrin are used. To detect prenatal exposure to these pesticides, maternal hair and blood, infant's hair, cord blood, and meconium were analyzed for the pesticides by gas chromatography/mass spectrometry. Infants were examined at 2 years of age with 95.1% follow up rate and their neurodevelopment outcome was assessed by the Griffiths mental developmental scale (N=754). Meconium analysis was the most sensitive method to detect fetal exposure to pesticides and exposure was highest for propoxur (21.3%) and the grouped pyrethroids (2.5% – bioallethrin, transfluthrin, cyfluthrin and cypermethrin). Path analysis modeling was performed to determine the effects of fetal exposure to propoxur and pyrethroids on the child's neurodevelopment at 24 months of age while controlling for confounders. Only singletons and those with complete data for the path analysis were included (N=696). Using a path analysis model, there was a significant negative (β=−0.14, p
ISSN:0161-813X
1872-9711
DOI:10.1016/j.neuro.2011.11.006