The Impact of Environmental Benzene, Toluene, Ethylbenzene, and Xylene Exposure on Blood-Based DNA Methylation Profiles in Pregnant African American Women from Detroit

Author:

Straughen Jennifer K.123,Loveless Ian1,Chen Yalei1,Burmeister Charlotte1,Lamerato Lois13,Lemke Lawrence D.4ORCID,O’Leary Brendan F.56ORCID,Reiners John J.78,Sperone F. Gianluca59,Levin Albert M.13,Cassidy-Bushrow Andrea E.1310

Affiliation:

1. Department of Public Health Sciences, Henry Ford Health, 1 Ford Place, Detroit, MI 48202, USA

2. Department of Obstetrics, Gynecology and Reproductive Biology, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA

3. Henry Ford Health + Michigan State University Health Sciences, Detroit, MI 48202, USA

4. Department of Earth and Atmospheric Sciences, Central Michigan University, Brooks Hall 314, Mount Pleasant, MI 48859, USA

5. Department of Civil and Environmental Engineering, Wayne State University, 2100 Engineering Building, Detroit, MI 48202, USA

6. Department of Biology, Wayne State University, 5047 Gullen Mall, Detroit, MI 48202, USA

7. Center for Urban Responses to Environmental Stressors, Wayne State University, 6135 Woodward Ave, Detroit, MI 48202, USA

8. Institute of Environmental Health Sciences, Wayne State University, 6135 Woodward Ave, Detroit, MI 48202, USA

9. Department of Environmental Science and Geology, Wayne State University, 4841 Cass Avenue, Detroit, MI 48201, USA

10. Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA

Abstract

African American women in the United States have a high risk of adverse pregnancy outcomes. DNA methylation is a potential mechanism by which exposure to BTEX (benzene, toluene, ethylbenzene, and xylenes) may cause adverse pregnancy outcomes. Data are from the Maternal Stress Study, which recruited African American women in the second trimester of pregnancy from February 2009 to June 2010. DNA methylation was measured in archived DNA from venous blood collected in the second trimester. Trimester-specific exposure to airshed BTEX was estimated using maternal self-reported addresses and geospatial models of ambient air pollution developed as part of the Geospatial Determinants of Health Outcomes Consortium. Among the 64 women with exposure and outcome data available, 46 differentially methylated regions (DMRs) were associated with BTEX exposure (FDR adjusted p-value < 0.05) using a DMR-based epigenome-wide association study approach. Overall, 89% of DMRs consistently exhibited hypomethylation with increasing BTEX exposure. Biological pathway analysis identified 11 enriched pathways, with the top 3 involving gamma-aminobutyric acid receptor signaling, oxytocin in brain signaling, and the gustation pathway. These findings highlight the potential impact of BTEX on DNA methylation in pregnant women.

Funder

Institute for Population Sciences, Health Assessment, Administration, Services, and Economics

Kellogg Foundation

Center for Leadership in Environmental Awareness and Research NIH

Center for Urban Response to Environmental Stressors NIH

Publisher

MDPI AG

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