The candidate's five-year career goal is to become an independent investigator in the areas of maternal nutrition and placental nutrient transport and metabolism. Her long-term career objective is to build a strong translational research program, utilizing appropriate animal models and human investigations to study the effect of maternal pre-pregnancy nutrition on placental growth and function, neonatal health, and the offspring's risk of future cardiovascular disease. It is becoming increasingly clear that the placenta plays a key role in the origin of adverse fetal outcomes resulting from maternal over- or under-nutrition. In keeping with this view, the placenta is an important element in the origins of adult chronic disease. The candidate has a strong scientific background in molecular biology, immunohistochemistry, primary cell culture and small and large animal surgery. She has gained expertise in fetal physiology (especially of the cardiovascular system) and is well-versed in the literature surrounding the developmental origins of health and cardiovascular disease. Additional training is required however before she can achieve her career goal of becoming an independent investigator in maternal-fetal health. The proposed training program has been designed to provide: 1) training in placental physiology and research methodologies, 2) experience in nutritional science and research methodologies and 3) in-depth training in human investigation. The Oregon Health and Science University is an ideal environment for this training. It offers its strong reputation as a leading biomedical research and training institution;the Heart Research Center is internationally recognized for its work in fetal physiology and the developmental origins of health and disease;the Oregon National Primate Research Center is internationally recognized for its translational research in pregnancy and the Oregon Clinical and Translational Research Institute is dedicated to the development of successful trainees and young investigators in translational and clinical research. One in five women who deliver in the United States is obese (body mass index (BMI) of >30 kg/m2). This condition is associated with both short- and long-term adverse consequences for mother and her baby. Such babies are at risk for developing chronic diseases including adult-onset coronary heart disease and the metabolic syndrome. Our preliminary data show that male offspring of overweight and obese mothers have lower levels of docosaehexanoic acid - a long chain polyunsaturated (LC-PUFA) derivative of essential fatty acids - than female offspring, while no differences in LC-PUFA levels exist between male and female offspring of lean women. Such deficiencies lead to neurological and vascular pathologies in the newborn. All of the essential LC-PUFA that are acquired by the fetus are actively transported across the placental barrier. The effect of maternal obesity on placental delivery of LC-PUFA to the fetus is unknown. Due to their rapid growth in utero, boys invest less in placental growth than girls and are at a greater risk of undernourishment and poor outcomes in response to stressful conditions. Maternal obesity exposes the placental-fetal unit to pro-inflammatory molecules. Inflammatory cytokines inhibit fatty acid uptake in the liver, muscle and heart. The effect of inflammatory cytokines on placental transport is not known. It is also unknown whether male fetuses and their placentas are more sensitive than females to maternal obesity and inflammation. The overall goal of this proposal is to determine the degree to which maternal obesity alters gender-specific fatty acid transport in the placenta. Studies will be conducted in our non-human primate model of maternal obesity from which we will establish the relationship between obesity and 3rd trimester placental fatty acid transport in vivo using stable isotope-labeled fatty acid tracers. Complementary studies in women will determine the degree to which maternal BMI and fetal sex alter placental lipid uptake. The roles of inflammatory cytokines in altering fatty acid uptake kinetics will be determined in placental tissue isolated from lean women with male or female offspring. These translational studies will determine the effect of maternal obesity, fetal sex and inflammatory cytokines on placental fat transport in a human population. Upon completion of the proposed studies, we will have determined 1) the degree to which maternal obesity alters uptake and transport of LC-PUFA in the late gestation non-human primate placenta, 2) the effect of fetal gender on placental LC-PUFA uptake in women at term and 3) mechanisms by which inflammatory cytokines suppress placental fatty acid uptake in vitro.

Public Health Relevance

The prevalence of obesity in women who give birth in the US is 1 in 5, which is associated with severe health consequences for both mother and child. Poor fetal nutrition during development due to maternal obesity is known to put the child at a higher risk of cardiovascular disease in later life. The proposed studies will help us understand how obesity during pregnancy alters the placental transfer of nutrients from mother to child and how this impacts neonatal nutrition.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Transition Award (R00)
Project #
4R00HD062841-03
Application #
8643321
Study Section
Special Emphasis Panel (NSS)
Program Officer
Ilekis, John V
Project Start
2013-05-01
Project End
2016-04-30
Budget Start
2013-05-01
Budget End
2014-04-30
Support Year
3
Fiscal Year
2013
Total Cost
$249,734
Indirect Cost
$84,314
Name
Metrohealth Medical Center
Department
Type
DUNS #
071124291
City
Cleveland
State
OH
Country
United States
Zip Code
44109
O'Tierney-Ginn, P F; Davina, D; Gillingham, M et al. (2017) Neonatal fatty acid profiles are correlated with infant growth measures at 6 months. J Dev Orig Health Dis 8:474-482
Berggren, E K; O'Tierney-Ginn, P; Lewis, S et al. (2017) Variations in resting energy expenditure: impact on gestational weight gain. Am J Obstet Gynecol 217:445.e1-445.e6
O'Tierney-Ginn, Perrie F; Gillingham, Melanie; Fowler, Jessica et al. (2017) Maternal Weight Gain Regulates Omega-3 Fatty Acids in Male, Not Female, Neonates. Reprod Sci 24:560-567
Calabuig-Navarro, Virtu; Haghiac, Maricela; Minium, Judi et al. (2017) Effect of Maternal Obesity on Placental Lipid Metabolism. Endocrinology 158:2543-2555
Calabuig-Navarro, Virtu; Puchowicz, Michelle; Glazebrook, Patricia et al. (2016) Effect of ?-3 supplementation on placental lipid metabolism in overweight and obese women. Am J Clin Nutr 103:1064-72
Yang, Xiaohua; Li, Ming; Haghiac, Maricela et al. (2016) Causal relationship between obesity-related traits and TLR4-driven responses at the maternal-fetal interface. Diabetologia 59:2459-2466
O'Tierney-Ginn, P; Roberts, V; Gillingham, M et al. (2015) Influence of high fat diet and resveratrol supplementation on placental fatty acid uptake in the Japanese macaque. Placenta 36:903-10
O'Tierney-Ginn, Perrie; Presley, Larraine; Myers, Stephen et al. (2015) Placental growth response to maternal insulin in early pregnancy. J Clin Endocrinol Metab 100:159-65
O'Tierney-Ginn, Perrie; Presley, Larraine; Minium, Judi et al. (2014) Sex-specific effects of maternal anthropometrics on body composition at birth. Am J Obstet Gynecol 211:292.e1-9
Abumaree, M H; Alahari, S; Albrecht, C et al. (2014) IFPA Meeting 2013 Workshop Report I: diabetes in pregnancy, maternal dyslipidemia in pregnancy, oxygen in placental development, stem cells and pregnancy pathology. Placenta 35 Suppl:S4-9

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