PMID- 23085522 OWN - NLM STAT- MEDLINE DCOM- 20130709 LR - 20151119 IS - 1872-9711 (Electronic) IS - 0161-813X (Linking) VI - 34 DP - 2013 Jan TI - Evaluating the neurotoxic effects of lactational exposure to persistent organic pollutants (POPs) in Spanish children. PG - 9-15 LID - S0161-813X(12)00249-5 [pii] LID - 10.1016/j.neuro.2012.10.006 [doi] AB - Although the brain continues developing in the postnatal period, epidemiological studies on the effects of postnatal exposure to neurotoxic POPs through breast-feeding remain mostly inconclusive. Failure to detect associations between postnatal exposure and health outcomes may stem from the limitations of commonly employed approaches to assess lactational exposure. The aim of the present study was to assess whether lactational exposure to polychlorinated biphenyl-153 (PCB-153), dichlorodiphenyldichloroethylene (DDE), or hexachlorobenzene (HCB) as estimated with a physiologically based pharmacokinetic (PBPK) model, is associated with decrements in mental and psychomotor development scores of the Bayley Scales of Infant Development (BSID) test in children aged around 14-months of a subsample (N=1175) of the Spanish INMA birth cohort, and to compare this with the effects of prenatal exposure. Although in the present study population PCB-153, DDE and HCB exposure increased within the first months of postnatal life, no associations were found between different periods of postnatal exposure to these compounds and mental or psychomotor scores. Increasing prenatal PCB-153 concentrations were associated with worse mental and psychomotor scores, although significance was only reached for psychomotor development (beta [95%CI]=-1.36 [-2.61, -0.11]). Indeed, the association between exposure and effects observed during prenatal life weakened gradually across periods of postnatal life. Results of the present study suggest that, although breastfeeding increases children's blood persistent organic pollutants (POPs) levels during postnatal life, deleterious effects of PCB-153 on neuropsychological development are mainly attributable to prenatal exposure. CI - Copyright (c) 2012 Elsevier Inc. All rights reserved. FAU - Gascon, Mireia AU - Gascon M AD - Centre for Research in Environmental Epidemiology, Dr. Aiguader 88, 08003 Barcelona, Catalonia, Spain. mgascon@creal.cat FAU - Verner, Marc-Andre AU - Verner MA FAU - Guxens, Monica AU - Guxens M FAU - Grimalt, Joan O AU - Grimalt JO FAU - Forns, Joan AU - Forns J FAU - Ibarluzea, Jesus AU - Ibarluzea J FAU - Lertxundi, Nerea AU - Lertxundi N FAU - Ballester, Ferran AU - Ballester F FAU - Llop, Sabrina AU - Llop S FAU - Haddad, Sami AU - Haddad S FAU - Sunyer, Jordi AU - Sunyer J FAU - Vrijheid, Martine AU - Vrijheid M LA - eng PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20121018 PL - Netherlands TA - Neurotoxicology JT - Neurotoxicology JID - 7905589 RN - 0 (Environmental Pollutants) RN - 4M7FS82U08 (Dichlorodiphenyl Dichloroethylene) RN - 4Z87H0LKUY (Hexachlorobenzene) RN - DFC2HB4I0K (Polychlorinated Biphenyls) RN - ZRU0C9E32O (2,4,5,2',4',5'-hexachlorobiphenyl) SB - IM MH - Age Factors MH - Brain/*drug effects/growth & development/metabolism/physiopathology MH - Breast Feeding/*adverse effects MH - Child Development/drug effects MH - Cognition/drug effects MH - Dichlorodiphenyl Dichloroethylene/*adverse effects/blood/pharmacokinetics MH - Environmental Pollutants/*adverse effects MH - Female MH - Hexachlorobenzene/*adverse effects/blood/pharmacokinetics MH - Humans MH - Infant MH - Infant, Newborn MH - *Lactation MH - Linear Models MH - Maternal Exposure/adverse effects MH - Milk, Human/*metabolism MH - Models, Biological MH - Neuropsychological Tests MH - Neurotoxicity Syndromes/blood/*etiology/physiopathology/psychology MH - Polychlorinated Biphenyls/*adverse effects/blood/pharmacokinetics MH - Pregnancy MH - Prenatal Exposure Delayed Effects MH - Psychomotor Performance/drug effects MH - Risk Assessment MH - Risk Factors MH - Spain EDAT- 2012/10/23 06:00 MHDA- 2013/07/10 06:00 CRDT- 2012/10/23 06:00 PHST- 2012/07/23 00:00 [received] PHST- 2012/09/17 00:00 [revised] PHST- 2012/10/09 00:00 [accepted] PHST- 2012/10/23 06:00 [entrez] PHST- 2012/10/23 06:00 [pubmed] PHST- 2013/07/10 06:00 [medline] AID - S0161-813X(12)00249-5 [pii] AID - 10.1016/j.neuro.2012.10.006 [doi] PST - ppublish SO - Neurotoxicology. 2013 Jan;34:9-15. doi: 10.1016/j.neuro.2012.10.006. Epub 2012 Oct 18.