Prenatal methylmercury exposure and DNA methylation in seven-year-old children in the Seychelles Child Development Study.

Journal: Environment international

Volume: 147

Issue: 

Year of Publication: 2021

Affiliated Institutions:  Institute of Environmental Medicine, Karolinska Institutet, Box , Stockholm, Sweden; Department of Organism Biology, Uppsala University, Kåbovägen , Uppsala, Sweden. Institute of Environmental Medicine, Karolinska Institutet, Box , Stockholm, Sweden. University of Rochester Medical Center, School of Medicine and Dentistry, Elmwood Ave, Rochester, NY , USA. Department of Laboratory Medicine, Division of Occupational and Environmental Medicine, Lund University, Scheelevägen , Lund, Sweden. the Child Development Centre, Ministry of Health, Mahé, Seychelles. Nutrition Innovation Centre for Food and Health (NICHE), Ulster University, Coleraine, Northern Ireland Bt SA, UK. Department of Organism Biology, Uppsala University, Kåbovägen , Uppsala, Sweden. Institute of Environmental Medicine, Karolinska Institutet, Box , Stockholm, Sweden; Department of Laboratory Medicine, Division of Occupational and Environmental Medicine, Lund University, Scheelevägen , Lund, Sweden. Electronic address: karin.broberg@ki.se.

Abstract summary 

Methylmercury (MeHg) is present in fish and is a neurotoxicant at sufficiently high levels. One potential mechanism of MeHg toxicity early in life is epigenetic dysregulation that may affect long-term neurodevelopment. Altered DNA methylation of nervous system-related genes has been associated with adult mental health outcomes.To assess associations between prenatal MeHg exposure and DNA methylation (at the cytosine of CG dinucleotides, CpGs) in three nervous system-related genes, encoding brain-derived neurotropic factor (BDNF), glutamate receptor subunit NR2B (GRIN2B), and the glucocorticoid receptor (NR3C1), in children who were exposed to MeHg in utero.We tested 406 seven-year-old Seychellois children participating in the Seychelles Child Development Study (Nutrition Cohort 2), who were prenatally exposed to MeHg from maternal fish consumption. Total mercury in maternal hair (prenatal MeHg exposure measure) collected during pregnancy was measured using atomic absorption spectroscopy. Methylation in DNA from the children's saliva was measured by pyrosequencing. To assess associations between prenatal MeHg exposure and CpG methylation at seven years of age, we used multivariable linear regression models adjusted for covariates.We identified associations with prenatal MeHg exposure for DNA methylation of one GRIN2B CpG and two NR3C1 CpGs out of 12 total CpG sites. Higher prenatal MeHg was associated with higher methylation for each CpG site. For example, NR3C1 CpG3 had an expected increase of 0.03-fold for each additional 1 ppm of prenatal MeHg (B = 0.030, 95% CI 0.001, 0.059; p = 0.047). Several CpG sites associated with MeHg are located in transcription factor binding sites and the observed methylation changes are predicted to lead to lower gene expression.In a population of people who consume large amounts of fish, we showed that higher prenatal MeHg exposure was associated with differential DNA methylation at seven years of age at specific CpG sites that may influence neurodevelopment and mental health.

Authors & Co-authors:  Cediel Ulloa Andrea A Gliga Anda A Love Tanzy M TM Pineda Daniela D Mruzek Daniel W DW Watson Gene E GE Davidson Philip W PW Shamlaye Conrad F CF Strain J J JJ Myers Gary J GJ van Wijngaarden Edwin E Ruegg Joelle J Broberg Karin K

Study Outcome 

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Citations : 
Authors :  13
Identifiers
Doi : 10.1016/j.envint.2020.106321
SSN : 1873-6750
Study Population
Female
Mesh Terms
Adult
Other Terms
DNA methylation;Early life;Epigenetic;Fish consumption;MeHg;Methylmercury;Neurodevelopment
Study Design
Cohort Study
Study Approach
Country of Study
Seychelles
Publication Country
Netherlands