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Published on: March 6, 2018
Associations between prenatal phthalate exposure and childhood epigenetic age acceleration
Dennis Khodasevich1, Nina Holland2, Alan Hubbard3
1Division of Environmental Health Sciences, School of Public Health, University of California, Berkeley, CA, USA; Center for Computational Biology, University of California, Berkeley, CA, USA.
Insights
Prenatal exposure to certain phthalates may impact children's epigenetic aging, particularly in males. This effect might be time-dependent, appearing at specific developmental stages rather than consistently across childhood.
Area of Science:
- Environmental Health
- Epigenetics
- Developmental Toxicology
Background:
- Phthalates are endocrine-disrupting chemicals linked to various health issues.
- Their effect on epigenetic aging biomarkers in children is not well understood.
- Prenatal phthalate exposure is widespread and may influence developmental trajectories.
Purpose of the Study:
- To investigate the association between prenatal phthalate exposure and epigenetic aging in children.
- To examine epigenetic age acceleration at birth and during childhood.
- To explore sex-specific patterns and the influence of exposure timing.
Main Methods:
- Analysis of 385 mother-child pairs from the CHAMACOS cohort.
- Measurement of DNA methylation (DNAm) at birth, 7, 9, and 14 years.
- Use of adjusted linear regression and quantile g-computation to assess associations between phthalate metabolites and epigenetic age acceleration (GAA and IEAA).
Main Results:
- A negative association was observed between prenatal di(2-ethylhexyl) phthalate (DEHP) exposure and intrinsic epigenetic age acceleration (IEAA) in 7-year-old males.
- A marginal negative association was found between the phthalate mixture and gestational age acceleration (GAA) in newborns, specifically males.
- Most other tested associations between phthalate exposure and epigenetic aging were not statistically significant.
Conclusions:
- Prenatal exposure to specific phthalates is associated with epigenetic aging in children.
- The impact of prenatal phthalate exposure on epigenetic age may be transient, manifesting only during certain developmental windows.
- Studies using single time-point DNAm measurements may miss crucial associations between phthalate exposure and epigenetic aging.
Background:
Phthalates, a group of pervasive endocrine-disrupting chemicals found in plastics and personal care products, have been associated with a wide range of developmental and health outcomes. However, their impact on biomarkers of aging has not been characterized. We tested associations between prenatal exposure to 11 phthalate metabolites on epigenetic aging in children at birth, 7, 9, and 14 years of age. We hypothesized that prenatal phthalate exposure will be associated with epigenetic age acceleration measures at birth and in early childhood, with patterns dependent on sex and timing of DNAm measurement.
Methods:
Among 385 mother-child pairs from the CHAMACOS cohort, we measured DNAm at birth, 7, 9, and 14 years of age, and utilized adjusted linear regression to assess the association between prenatal phthalate exposure and Bohlin's Gestational Age Acceleration (GAA) at birth and Intrinsic Epigenetic Age Acceleration (IEAA) throughout childhood. Additionally, quantile g-computation was utilized to assess the effect of the phthalate mixture on GAA at birth and IEAA throughout childhood.
Results:
We found a negative association between prenatal di (2-ethylhexyl) phthalate (DEHP) exposure and IEAA among males at age 7 (-0.62 years; 95% CI:-1.06 to -0.18), and a marginal negative association between the whole phthalate mixture and GAA among males at birth (-1.54 days, 95% CI: -2.79 to -0.28), while most other associations were nonsignificant.
Conclusions:
Our results suggest that prenatal exposure to certain phthalates is associated with epigenetic aging in children. Additionally, our findings suggest that the influence of prenatal exposures on epigenetic age may only manifest during specific periods of child development, and studies relying on DNAm measurements solely from cord blood or single time points may overlook potential relationships.
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