Prenatal exposure to organochlorine compounds and lung function during childhood
Introduction: Prenatal exposure to organochlorine compounds (OCs) can increase the risk of reported respiratory symptoms in children. It remains unclear whether these compounds can also impact on lung function. We assessed the association between prenatal exposure to OCs and lung function during childhood. Methods: We included 1308 mother-child pairs enrolled in a prospective cohort study. Prenatal concentrations of p,p′-dichlorodiphenyltrichloroethane [p,p′-DDT], p,p′-dichlorodiphenyldichloroethylene [p,p′-DDE], hexachlorobenzene [HCB], and seven polychlorinated biphenyls [PCBs] were measured in cord blood. Spirometry was performed in the offspring at ages 4 (n = 636) and 7 years (n = 1192). Results: More than 80% of samples presented quantifiable levels of p,p′-DDE, HCB, PCB-138, PCB-153, and PCB-180; p,p′-DDE was the compound with the highest median concentrations. At 4 years, prenatal p,p′-DDE exposure was associated with a decrease in forced expiratory volume in 1 s (FEV1) in all quartiles of exposure (e.g., third quartile [0.23–0.34 ng/mL]: β for FEV1 −53.61 mL, 95% CI −89.87, −17.35, vs. the lowest). Prenatal p,p′-DDE levels also decreased forced vital capacity (FVC) and FEV1/FVC, but associations did not reach statistical significance in most exposure quartiles. At 7 years, p,p′-DDE was associated with a decrease in FVC and FEV1 in only the second quartile of exposure (e.g. β for FEV1 −36.96 mL, 95% CI −66.22, −7.70, vs. the lowest). Prenatal exposure to HCB was associated with decreased FVC and FEV1, but in only the second quartile and at 7 years (e.g. [0.07–0.14 ng/mL]: β for FEV1 −25.79 mL, 95% CI −55.98, 4.39, vs. the lowest). PCBs were not consistently associated with lung function. Conclusion: Prenatal exposure to p,p′-DDE may decrease lung function during childhood, especially FEV1 and at medium levels of exposure. Further and deeper knowledge on the impact of environmental chemicals during pregnancy on lung development is needed. © 2019 The Authors
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Format: | artículo biblioteca |
Language: | English |
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Elsevier
2019-10
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Subjects: | Birth cohort, Children, Lung function, Dichlorodiphenyldichloroethylene, Prenatal exposure, Organochlorine compounds, |
Online Access: | http://hdl.handle.net/10261/199561 http://dx.doi.org/10.13039/501100000780 |
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Birth cohort Children Lung function Dichlorodiphenyldichloroethylene Prenatal exposure Organochlorine compounds Birth cohort Children Lung function Dichlorodiphenyldichloroethylene Prenatal exposure Organochlorine compounds |
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Birth cohort Children Lung function Dichlorodiphenyldichloroethylene Prenatal exposure Organochlorine compounds Birth cohort Children Lung function Dichlorodiphenyldichloroethylene Prenatal exposure Organochlorine compounds Abellan, Alicia Sunyer, Jordi García-Esteban, Raquel Basterrechea, Mikel Duarte-Salles, Talita Ferrero, Amparo Garcia-Aymerich, Judith Gascon, Mireia Grimalt, Joan O. Lopez-Espinosa, Maria-Jose Zabaleta, Carlos Vrijheid, Martine Casas, Maribel Prenatal exposure to organochlorine compounds and lung function during childhood |
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Introduction: Prenatal exposure to organochlorine compounds (OCs) can increase the risk of reported respiratory symptoms in children. It remains unclear whether these compounds can also impact on lung function. We assessed the association between prenatal exposure to OCs and lung function during childhood. Methods: We included 1308 mother-child pairs enrolled in a prospective cohort study. Prenatal concentrations of p,p′-dichlorodiphenyltrichloroethane [p,p′-DDT], p,p′-dichlorodiphenyldichloroethylene [p,p′-DDE], hexachlorobenzene [HCB], and seven polychlorinated biphenyls [PCBs] were measured in cord blood. Spirometry was performed in the offspring at ages 4 (n = 636) and 7 years (n = 1192). Results: More than 80% of samples presented quantifiable levels of p,p′-DDE, HCB, PCB-138, PCB-153, and PCB-180; p,p′-DDE was the compound with the highest median concentrations. At 4 years, prenatal p,p′-DDE exposure was associated with a decrease in forced expiratory volume in 1 s (FEV1) in all quartiles of exposure (e.g., third quartile [0.23–0.34 ng/mL]: β for FEV1 −53.61 mL, 95% CI −89.87, −17.35, vs. the lowest). Prenatal p,p′-DDE levels also decreased forced vital capacity (FVC) and FEV1/FVC, but associations did not reach statistical significance in most exposure quartiles. At 7 years, p,p′-DDE was associated with a decrease in FVC and FEV1 in only the second quartile of exposure (e.g. β for FEV1 −36.96 mL, 95% CI −66.22, −7.70, vs. the lowest). Prenatal exposure to HCB was associated with decreased FVC and FEV1, but in only the second quartile and at 7 years (e.g. [0.07–0.14 ng/mL]: β for FEV1 −25.79 mL, 95% CI −55.98, 4.39, vs. the lowest). PCBs were not consistently associated with lung function. Conclusion: Prenatal exposure to p,p′-DDE may decrease lung function during childhood, especially FEV1 and at medium levels of exposure. Further and deeper knowledge on the impact of environmental chemicals during pregnancy on lung development is needed. © 2019 The Authors |
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European Commission |
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European Commission Abellan, Alicia Sunyer, Jordi García-Esteban, Raquel Basterrechea, Mikel Duarte-Salles, Talita Ferrero, Amparo Garcia-Aymerich, Judith Gascon, Mireia Grimalt, Joan O. Lopez-Espinosa, Maria-Jose Zabaleta, Carlos Vrijheid, Martine Casas, Maribel |
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artículo |
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Birth cohort Children Lung function Dichlorodiphenyldichloroethylene Prenatal exposure Organochlorine compounds |
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Abellan, Alicia Sunyer, Jordi García-Esteban, Raquel Basterrechea, Mikel Duarte-Salles, Talita Ferrero, Amparo Garcia-Aymerich, Judith Gascon, Mireia Grimalt, Joan O. Lopez-Espinosa, Maria-Jose Zabaleta, Carlos Vrijheid, Martine Casas, Maribel |
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Abellan, Alicia |
title |
Prenatal exposure to organochlorine compounds and lung function during childhood |
title_short |
Prenatal exposure to organochlorine compounds and lung function during childhood |
title_full |
Prenatal exposure to organochlorine compounds and lung function during childhood |
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Prenatal exposure to organochlorine compounds and lung function during childhood |
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Prenatal exposure to organochlorine compounds and lung function during childhood |
title_sort |
prenatal exposure to organochlorine compounds and lung function during childhood |
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Elsevier |
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2019-10 |
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http://hdl.handle.net/10261/199561 http://dx.doi.org/10.13039/501100000780 |
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AT abellanalicia prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT sunyerjordi prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT garciaestebanraquel prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT basterrecheamikel prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT duartesallestalita prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT ferreroamparo prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT garciaaymerichjudith prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT gasconmireia prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT grimaltjoano prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT lopezespinosamariajose prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT zabaletacarlos prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT vrijheidmartine prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood AT casasmaribel prenatalexposuretoorganochlorinecompoundsandlungfunctionduringchildhood |
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dig-idaea-es-10261-1995612022-06-23T10:34:30Z Prenatal exposure to organochlorine compounds and lung function during childhood Abellan, Alicia Sunyer, Jordi García-Esteban, Raquel Basterrechea, Mikel Duarte-Salles, Talita Ferrero, Amparo Garcia-Aymerich, Judith Gascon, Mireia Grimalt, Joan O. Lopez-Espinosa, Maria-Jose Zabaleta, Carlos Vrijheid, Martine Casas, Maribel European Commission Grimalt, Joan O. [0000-0002-7391-5768] Birth cohort Children Lung function Dichlorodiphenyldichloroethylene Prenatal exposure Organochlorine compounds Introduction: Prenatal exposure to organochlorine compounds (OCs) can increase the risk of reported respiratory symptoms in children. It remains unclear whether these compounds can also impact on lung function. We assessed the association between prenatal exposure to OCs and lung function during childhood. Methods: We included 1308 mother-child pairs enrolled in a prospective cohort study. Prenatal concentrations of p,p′-dichlorodiphenyltrichloroethane [p,p′-DDT], p,p′-dichlorodiphenyldichloroethylene [p,p′-DDE], hexachlorobenzene [HCB], and seven polychlorinated biphenyls [PCBs] were measured in cord blood. Spirometry was performed in the offspring at ages 4 (n = 636) and 7 years (n = 1192). Results: More than 80% of samples presented quantifiable levels of p,p′-DDE, HCB, PCB-138, PCB-153, and PCB-180; p,p′-DDE was the compound with the highest median concentrations. At 4 years, prenatal p,p′-DDE exposure was associated with a decrease in forced expiratory volume in 1 s (FEV1) in all quartiles of exposure (e.g., third quartile [0.23–0.34 ng/mL]: β for FEV1 −53.61 mL, 95% CI −89.87, −17.35, vs. the lowest). Prenatal p,p′-DDE levels also decreased forced vital capacity (FVC) and FEV1/FVC, but associations did not reach statistical significance in most exposure quartiles. At 7 years, p,p′-DDE was associated with a decrease in FVC and FEV1 in only the second quartile of exposure (e.g. β for FEV1 −36.96 mL, 95% CI −66.22, −7.70, vs. the lowest). Prenatal exposure to HCB was associated with decreased FVC and FEV1, but in only the second quartile and at 7 years (e.g. [0.07–0.14 ng/mL]: β for FEV1 −25.79 mL, 95% CI −55.98, 4.39, vs. the lowest). PCBs were not consistently associated with lung function. Conclusion: Prenatal exposure to p,p′-DDE may decrease lung function during childhood, especially FEV1 and at medium levels of exposure. Further and deeper knowledge on the impact of environmental chemicals during pregnancy on lung development is needed. © 2019 The Authors Funding text #1 This study was funded by grants from Instituto de Salud Carlos III ( FIS-PI06/0867 and FIS-PI09/00090 ), CIBERESP, Department of Health of the Basque Government ( 2005111093 , 2009111069 , 2013111089 and 2015111065 ), and the Provincial Government of Gipuzkoa ( DFG06/002 , DFG08/001 and DFG15/221 ) and annual agreements with the municipalities of the study area (Zumarraga, Urretxu, Legazpi, Azkoitia y Azpeitia y Beasain). Funding text #2 This study was funded by grants from Instituto de Salud Carlos III ( Red INMA G03/176 ; CB06/02/0041 ; PI041436 ; PI081151 incl. FEDER funds; CP16/00128 ), CIBERESP , Generalitat de Catalunya - CIRIT 1999SGR 00241 , Generalitat de Catalunya- AGAUR 2009 SGR 501 , Fundació La marató de TV3 ( 090430 ), EU Commission ( 261357 ). ISGlobal is a member of the CERCA Programme, Generalitat de Catalunya. Funding text #3 This study was funded by Grants from UE ( FP7-ENV-2011 cod 282957 and HEALTH.2010.2.4.5-1 ), Instituto de Salud Carlos III ( G03/176 ; FIS-FEDER : PI11/01007 , PI11/02591 , PI11/02038 , PI12/00610 , PI13/1944 , PI13/2032 , PI14/00891 , PI14/01687 , PI16/1288 , and PI17/0663 ; Miguel Servet -FEDER CP11/00178 , CP15/00025 , and MSII16/00051 ), Alicia Koplowitz Foundation 2017, and Generalitat Valenciana : FISABIO ( UGP 15-230 , UGP-15-244 , and UGP-15-249 ). Peer reviewed 2020-02-04T08:04:39Z 2020-02-04T08:04:39Z 2019-10 artículo http://purl.org/coar/resource_type/c_6501 Environment International 131: 105049 (2019) http://hdl.handle.net/10261/199561 10.1016/j.envint.2019.105049 http://dx.doi.org/10.13039/501100000780 en #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/EC/FP7/282957 info:eu-repo/grantAgreement/EC/FP7/261357 Publisher's version https://doi.org/10.1016/j.envint.2019.105049 Sí open Elsevier |