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CYP3A genes and the association between prenatal methylmercury exposure and neurodevelopment

Llop, Sabrina (author)
Jaume I University,CIBER Epidemiology and Public Health (CIBERESP)
Tran, N. V. (author)
University of Rochester
Ballester, Ferran (author)
Jaume I University,CIBER Epidemiology and Public Health (CIBERESP)
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Barbone, Fabio (author)
University of Udine,Burlo Garofolo Pediatric Institute
Sofianou-Katsoulis, Aikaterini (author)
Institute of Child Health
Sunyer, Jordi (author)
CIBER Epidemiology and Public Health (CIBERESP),Centre for Research in Environmental Epidemiology,Pompeu Fabra University,Hospital del Mar Medical Research Institute
Engström, Karin (author)
Lund University,Lunds universitet,Avdelningen för arbets- och miljömedicin,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Occupational and Environmental Medicine, Lund University,Department of Laboratory Medicine,Faculty of Medicine
Alhamdow, Ayman (author)
Karolinska Institute
Love, Tanzy M (author)
University of Rochester,CIBER Epidemiology and Public Health (CIBERESP),Jaume I University,University of Udine
Watson, Gene E (author)
University of Rochester
Bustamante, Mariona (author)
Centre for Research in Environmental Epidemiology,Center for Genomic Regulation (CRG),CIBER Epidemiology and Public Health (CIBERESP),Hospital del Mar Medical Research Institute
Murcia, Mario (author)
CIBER Epidemiology and Public Health (CIBERESP),Jaume I University
Iñiguez, Carmen (author)
Jaume I University,CIBER Epidemiology and Public Health (CIBERESP)
Shamlaye, Conrad F (author)
Ministry of Health, Seychelles
Rosolen, Valentina (author)
University of Udine
Mariuz, Marika (author)
University of Udine
Horvat, Milena (author)
Jožef Stefan Institute
Tratnik, Janja Snoj (author)
Jožef Stefan Institute
Mazej, Darja (author)
Jožef Stefan Institute
van Wijngaarden, Edwin (author)
University of Rochester
Davidson, Philip W (author)
University of Rochester
Myers, Gary J. (author)
University of Rochester
Rand, Matthew D. (author)
University of Rochester
Broberg, Karin (author)
Karolinska Institutet,Karolinska Institute
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 (creator_code:org_t)
Elsevier BV, 2017
2017
English 9 s.
In: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 105, s. 34-42
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background 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. Objectives We evaluated whether genetic variation in CYP3A genes influences the association between prenatal exposure to MeHg and child neuropsychological development. Methods The study population included 2639 children from three birth cohort studies: two subcohorts in Seychelles (SCDS) (n = 1160, 20 and 30 months of age, studied during the years 2001–2012), two subcohorts from Spain (INMA) (n = 625, 14 months of age, 2003–2009), and two subcohorts from Italy and Greece (PHIME) (n = 854, 18 months 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). Results 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. Conclusions Our results suggest that the polymorphisms in CYP3A genes may modify the response to dietary MeHg exposure during early life development.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Arbetsmedicin och miljömedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Occupational Health and Environmental Health (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Keyword

Birth cohort
Cognitive
CYP3A polymorphisms
Methylmercury
Neurotoxicity
Prenatal exposure

Publication and Content Type

art (subject category)
ref (subject category)

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