PROJECT 2 ABSTRACT Perfluoroalkyl substances (PFASs) are widely used synthetic chemicals present in nonstick coatings, food packaging, and water repellant clothing. Perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), perfluorononanoic acid (PFNA), and perfluorohexane sulfonate (PFHxS) are the four primary PFASs found in human blood samples in United States. There is accumulating evidence to suggest that PFAS exposures during the sensitive windows of pregnancy and gestation may adversely affect hormones involved in metabolism and adipogenesis. Specifically, exposure to PFASs during pregnancy/in utero may be related to excessive pregnancy-related weight gain, reduced duration of breastfeeding following pregnancy, and increased risk of overweight or obesity during childhood. These are important outcomes because e xcessive weight gain during pregnancy confers lifelong risk of morbidity for mothers and infants alike; a shortened duration of breastfeeding reduces the associated health benefits for both mother and child, and overweight/obesity during childhood increases long term risk of diabetes, hypertension, and other serious health disorders for affected children. Thus,identifying modifiable risk factors for these conditions has become a public health priority. By taking advantage of data and existing biological samples from women and children enrolled in the New Hampshire Birth Cohort Study, we will determine whether women with higher exposures to PFAS during pregnancy/gestation have greater risks for: 1) excessive weight gain during pregnancy, 2) shorter duration of breastfeeding or altered breast milk composition, and 3) offspring with greater childhood adiposity through age 5. We will also explore whether pregnancy weight gain or duration of breastfeeding are mediators of the association between prenatal PFAS exposures and adiposity at age 5. The United States for PFOA and PFOS. levated levels of these substances have been detected in drinking water supplies throughout the United States including in Northern New England PFAS exposures are preventable. Our study will provide critical data to inform policy reform and Environmental Protection Agency recently established drinking water health advisories E . identify possible opportunities to reduce or prevent PFAS exposure and thus improve the lifelong health of women and children.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM104416-09
Application #
10091540
Study Section
Special Emphasis Panel (ZGM1)
Project Start
2013-03-01
Project End
2023-01-31
Budget Start
2021-02-01
Budget End
2022-01-31
Support Year
9
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Type
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
Fricano-Kugler, Catherine J; Getz, Stephanie A; Williams, Michael R et al. (2018) Nuclear Excluded Autism-Associated Phosphatase and Tensin Homolog Mutations Dysregulate Neuronal Growth. Biol Psychiatry 84:265-277
Moen, Erika L; Kapadia, Nirav S; O'Malley, A James et al. (2018) Evaluating breast cancer care coordination at a rural National Cancer Institute Comprehensive Cancer Center using network analysis and geospatial methods. Cancer Epidemiol Biomarkers Prev :
Vergo, Maxwell T; Pinkson, Briane M; Broglio, Kathleen et al. (2018) Immediate Symptom Relief After a First Session of Massage Therapy or Reiki in Hospitalized Patients: A 5-Year Clinical Experience from a Rural Academic Medical Center. J Altern Complement Med 24:801-808
Hoen, Anne G; Madan, Juliette C; Li, Zhigang et al. (2018) Sex-specific associations of infants' gut microbiome with arsenic exposure in a US population. Sci Rep 8:12627
Barr, Fiona D; Ochsenbauer, Christina; Wira, Charles R et al. (2018) Neutrophil extracellular traps prevent HIV infection in the female genital tract. Mucosal Immunol 11:1420-1428
Signes-Pastor, Antonio J; Cottingham, Kathryn L; Carey, Manus et al. (2018) Infants' dietary arsenic exposure during transition to solid food. Sci Rep 8:7114
Salas, Lucas A; Koestler, Devin C; Butler, Rondi A et al. (2018) An optimized library for reference-based deconvolution of whole-blood biospecimens assayed using the Illumina HumanMethylationEPIC BeadArray. Genome Biol 19:64
Deyssenroth, Maya A; Gennings, Chris; Liu, Shelley H et al. (2018) Intrauterine multi-metal exposure is associated with reduced fetal growth through modulation of the placental gene network. Environ Int 120:373-381
Romano, Megan E; Eliot, Melissa N; Zoeller, R Thomas et al. (2018) Maternal urinary phthalate metabolites during pregnancy and thyroid hormone concentrations in maternal and cord sera: The HOME Study. Int J Hyg Environ Health 221:623-631
Everson, Todd M; Punshon, Tracy; Jackson, Brian P et al. (2018) Cadmium-Associated Differential Methylation throughout the Placental Genome: Epigenome-Wide Association Study of Two U.S. Birth Cohorts. Environ Health Perspect 126:017010

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