Epigenetic and Developmental Effects of In Utero Exposure to Environmental Toxicants

Early Life Exposure to Polycyclic Aromatic Hydrocarbons: Metabolic Perturbations and Epigenetic Biomarkers

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01815385

Enrollment

110

Registered

2013-03-21

Start date

2013-03-31

Completion date

2020-03-28

Last updated

2021-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adiposity, Environmental Exposures, Full Term Infants

Keywords

Term gestation, Environmental exposure, Benzo(a)pyrene, Polycyclic aromatic hydrocarbons, Adiposity, Cytosine methylation

Brief summary

Metabolic diseases such as obesity and diabetes are modern day epidemics. Early life exposure to an adverse developmental environment, including environmental toxins, are linked to increased susceptibility to obesity, metabolic syndrome and type 2 diabetes. Although the mechanisms underlying the fetal origins of metabolic disease are poorly understood, strong evidence suggests that alterations in the epigenome play a critical role in this process. The central hypothesis of this proposal is that intrauterine exposure to benzo\[a\]pyrene leads to epigenetic changes which will have functional consequences and may be a marker for, or may contribute to, increased susceptibility to adverse outcomes in childhood including increased adiposity and the subsequent development of obesity, metabolic syndrome or diabetes. The goals of this proposal are to: 1) determine benzo\[a\]pyrene levels in umbilical cord blood of newborns, 2) determine whether benzo\[a\]pyrene exposure during pregnancy correlates with early onset of obesity and metabolic disease by examining the children at 12 and 24 months of age, 3) determine whether in utero benzo\[a\]pyrene exposure programs metabolic disease through alterations in DNA methylation and gene expression, and 4) determine the plasticity of the DNA methylation patterns in the same offspring at 12 months of age. The long-term goal of this project is to define biomarkers that identify neonates at high-risk for diminished attainment of full health potential, who can then be targeted for preventative measures.

Interventions

None listed

Study design

Observational model

ECOLOGIC_OR_COMMUNITY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

1 Hours to 72 Hours

Healthy volunteers

Yes

Inclusion criteria

* Infants whose mothers were followed by the Obstetric Department at MMC, and * Deliver a single healthy live term infant

Exclusion criteria

* Multiple gestation, * Maternal depression, * History of maternal smoking in the 3rd trimester of pregnancy, * Infants in extremis, * Apgar score \<7 at 5 min and umbilical artery pH ≤7.25, * Chromosomal/congenital abnormalities, * Congenital infections, and * Inborn errors of metabolism

Design outcomes

Primary

Measure	Time frame	Description
Measure indices of adiposity in enrolled patients	up to 24 months	Assessments will be performed within 72 hours of birth and at 1 and 2 years of age.
Measure benzo(a)pyrene levels in blood samples	up to 12 months of age	Benzo(a)pyrene levels will be measured in cord blood samples obtained at birth and in peripheral blood samples obtained at 12 months of age.
Measure tobacco by-products in blood samples	up to 12 months of age	Levels of tobacco by-products will be measured in cord blood samples obtained at birth and in peripheral blood samples obtained at 12 months of age.
Characterize cytosine methylation changes in CD3+ T-lymphocytes	up to 12 months of age	Cytosine methylation changes in CD3+ T-lymphocytes will be characterized in cord blood and in a peripheral blood sample obtained at 12 months of age.

Countries

United States

Outcome results