The overall aim of this application is to assess the role of the maternal and offspring genotype on the long-term impact of prenatal docosahexaenoic acid (DHA) on child growth and development through age 5 y. In order to achieve this, we propose to use information from the follow-up of a trial of prenatal DHA supplementation on child growth and development. This double-blind clinical trial, in which 1,094 pregnant women (18-35 y) who sought prenatal care at the Instituto Mexicano del Seguro Social General Hospital and related clinics in Cuernavaca, Mexico were randomized to receive either 400 mg of DHA or a placebo daily from mid pregnancy through delivery, was conducted between 2004 and 2005. A large body of information has been collected since including offspring anthropometric measurements at 5 different time points from birth to 5 y, as well as measures of global cognitive development at up to 3 different time points for over 80% of the life births (n=802/973). To this date the trial has resulted in heterogeneous effects on birth-weight and infant growth and global cognitive development, and more recently, a significant improvement in offspring's attention at 5 y. Besides the large pool of information available on child growth and development, we have information on maternal FADS genotype, which plays a key role in fatty acid metabolism and availability for the offspring at early stages, for approximately 700 mothers. For this analysis, we propose to use all the available data and assay the banked offspring biospecimens to demonstrate the role of both maternal and child FADS genotype on long-term growth and development within the context of a DHA supplementation RCT. We will use longitudinal data analysis techniques to assess the role of maternal and offspring Single Nucleotide Polymorphisms and haplotypes in the FADS region, on determining growth and development at different stages from birth to 5y, and as modulators of a prenatal DHA supplementation intervention. This represents a unique opportunity to broaden our understanding of the role of genetics on the metabolism of long-chain polyunsaturated fatty acids and its long-term impact on child development. Results from this study will potentially contribute to improve the design and targeting of DHA supplementation interventions and strengthen their public health impact.

Public Health Relevance

Recent evidence suggests that genetic makeup plays an important role in essential fatty acid metabolism, which are particularly important for child growth and development. We plan to use the information available on from a prenatal n-3 fatty acid (DHA) supplementation trial implemented in Mexico in 2004, to assess the role of genetics in modifying the impact of prenatal DHA on child growth and cognitive development from birth through 5 years. Results will improve our understanding of the role of genetics and could help identify children and populations who are likely to benefit the most from prenatal DHA supplementation.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Small Research Grants (R03)
Project #
1R03HD087606-01A1
Application #
9318004
Study Section
Obstetrics and Maternal-Fetal Biology Subcommittee (CHHD-B)
Program Officer
Raiten, Daniel J
Project Start
2017-04-01
Project End
2019-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
1
Fiscal Year
2017
Total Cost
$78,000
Indirect Cost
$28,000
Name
Emory University
Department
Public Health & Prev Medicine
Type
Schools of Public Health
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Gonzalez-Casanova, Ines; Stein, Aryeh D; Barraza-Villarreal, Albino et al. (2018) Prenatal exposure to environmental pollutants and child development trajectories through 7 years. Int J Hyg Environ Health 221:616-622