CYP3A genes and the association between prenatal methylmercury exposure and neurodevelopment.

Journal: Environment international

Volume: 105

Issue: 

Year of Publication: 2018

Affiliated Institutions:  Epidemiology and Environmental Health Joint Research Unit, FISABIO-Universitat Jaume I-Universitat de València, Av. Catalunya , Valencia, Spain; Spanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Av. Monforte de Lemos, -. Pabellón , Madrid, Spain. University of Rochester Medical Center, School of Medicine and Dentistry, Elmwood Ave, Box , Rochester, NY , USA. Department of Medical and Biological Sciences, University of Udine, via Colugna , Udine, Italy; Institute for Maternal and Child Health IRCCS "Burlo Garofolo", via dell'Istria /, Trieste, Italy. Department of Social and Developmental Paediatrics, Institute of Child Health, Athens, Greece. Spanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Av. Monforte de Lemos, -. Pabellón , Madrid, Spain; ISGlobal, Centre for Research in Environmental Epidemiology (CREAL), Av. Aiguader , Barcelona, Spain; IMIM (Hospital del Mar Medical Research Institute), Av. Aiguader , Barcelona, Spain; Universitat Pompeu Fabra (UPF), Av. Aiguader , Barcelona, Spain. Division of Occupational and Environmental Medicine, Lund University, Lund, Sweden. Institute of Environmental Medicine, Karolinska Institutet, Nobels väg , Stockholm, Sweden. Spanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Av. Monforte de Lemos, -. Pabellón , Madrid, Spain; ISGlobal, Centre for Research in Environmental Epidemiology (CREAL), Av. Aiguader , Barcelona, Spain; IMIM (Hospital del Mar Medical Research Institute), Av. Aiguader , Barcelona, Spain; Genomics and Disease Group, Bioinformatics and Genomics Program, Centre for Genomic Regulation (CRG), Av. Aiguader , Barcelona, Spain. The Child Development Centre, Ministry of Health, Mahé, Seychelles. Department of Medical and Biological Sciences, University of Udine, via Colugna , Udine, Italy. Department of Environmental Sciences, Jozef Stefan Institute, Jamova cesta , Si- Ljubljana, Slovenia. Institute of Environmental Medicine, Karolinska Institutet, Nobels väg , Stockholm, Sweden. Electronic address: karin.broberg@ki.se.

Abstract summary 

Results on the association between prenatal exposure to methylmercury (MeHg) and child neuropsychological development are heterogeneous. Underlying genetic differences across study populations could contribute to this varied response to MeHg. Studies in Drosophila have identified the cytochrome p450 3A (CYP3A) family as candidate MeHg susceptibility genes.We evaluated whether genetic variation in CYP3A genes influences the association between prenatal exposure to MeHg and child neuropsychological development.The study population included 2639 children from three birth cohort studies: two subcohorts in Seychelles (SCDS) (n=1160, 20 and 30months of age, studied during the years 2001-2012), two subcohorts from Spain (INMA) (n=625, 14months of age, 2003-2009), and two subcohorts from Italy and Greece (PHIME) (n=854, 18months of age, 2006-2011). Total mercury, as a surrogate of MeHg, was analyzed in maternal hair and/or cord blood samples. Neuropsychological development was evaluated using Bayley Scales of Infant Development (BSID). Three functional polymorphisms in the CYP3A family were analyzed: rs2257401 (CYP3A7), rs776746 (CYP3A5), and rs2740574 (CYP3A4).There was no association between CYP3A polymorphisms and cord mercury concentrations. The scores for the BSID mental scale improved with increasing cord blood mercury concentrations for carriers of the most active alleles (β[95% CI]:=2.9[1.53,4.27] for CYP3A7 rs2257401 GG+GC, 2.51[1.04,3.98] for CYP3A5 rs776746 AA+AG and 2.31[0.12,4.50] for CYP3A4 rs2740574 GG+AG). This association was near the null for CYP3A7 CC, CYP3A5 GG and CYP3A4 AA genotypes. The interaction between the CYP3A genes and total mercury was significant (p<0.05) in European cohorts only.Our results suggest that the polymorphisms in CYP3A genes may modify the response to dietary MeHg exposure during early life development.

Authors & Co-authors:  Llop Sabrina S Tran Van V Ballester Ferran F Barbone Fabio F Sofianou-Katsoulis Aikaterini A Sunyer Jordi J Engström Karin K Alhamdow Ayman A Love Tanzy M TM Watson Gene E GE Bustamante Mariona M Murcia Mario M Iñiguez Carmen C Shamlaye Conrad F CF Rosolen Valentina V Mariuz Marika M Horvat Milena M Tratnik Janja S JS Mazej Darja D van Wijngaarden Edwin E Davidson Philip W PW Myers Gary J GJ Rand Matthew D MD Broberg Karin K

Study Outcome 

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Statistics
Citations :  Amunom I, Dieter LJ, Tamasi V, Cai J, Conklin DJ, Srivastava S, Martin MV, Guengerich FP, Prough RA. Cytochromes P450 catalyze the reduction of α,β-unsaturated aldehydes. Chem Res Toxicol. 2011;24:1223–1230.
Authors :  24
Identifiers
Doi : 10.1016/j.envint.2017.04.013
SSN : 1873-6750
Study Population
Female
Mesh Terms
Adult
Other Terms
Birth cohort;CYP3A polymorphisms;Cognitive;Methylmercury;Neurotoxicity;Prenatal exposure
Study Design
Cohort Study
Study Approach
Country of Study
Seychelles
Publication Country
Netherlands