Developmental pathways to adiposity begin before birth and are influenced by genotype, prenatal environment and epigenome.

Authors:
Xinyi Lin
Xinyi Lin
Harvard School of Public Health
United States
Ives Yubin Lim
Ives Yubin Lim
Singapore Institute for Clinical Sciences
Singapore
Yonghui Wu
Yonghui Wu
School of Biomedical Informatics
Houston | United States
Ai Ling Teh
Ai Ling Teh
Singapore Institute for Clinical Sciences
Li Chen
Li Chen
Jiangsu Marine Resources Development Research Institute
China
Izzuddin M Aris
Izzuddin M Aris
Yong Loo Lin School of Medicine
Shu E Soh
Shu E Soh
Singapore Institute for Clinical Sciences
Singapore
Mya Thway Tint
Mya Thway Tint
Yong Loo Lin School of Medicine
Singapore

BMC Med 2017 03 7;15(1):50. Epub 2017 Mar 7.

Singapore Institute for Clinical Sciences, A*STAR, 30 Medical Drive, Singapore, 117609, Singapore.

Background: Obesity is an escalating health problem worldwide, and hence the causes underlying its development are of primary importance to public health. There is growing evidence that suboptimal intrauterine environment can perturb the metabolic programing of the growing fetus, thereby increasing the risk of developing obesity in later life. However, the link between early exposures in the womb, genetic susceptibility, and perturbed epigenome on metabolic health is not well understood. In this study, we shed more light on this aspect by performing a comprehensive analysis on the effects of variation in prenatal environment, neonatal methylome, and genotype on birth weight and adiposity in early childhood.

Methods: In a prospective mother-offspring cohort (N = 987), we interrogated the effects of 30 variables that influence the prenatal environment, umbilical cord DNA methylation, and genotype on offspring weight and adiposity, over the period from birth to 48 months. This is an interim analysis on an ongoing cohort study.

Results: Eleven of 30 prenatal environments, including maternal adiposity, smoking, blood glucose and plasma unsaturated fatty acid levels, were associated with birth weight. Polygenic risk scores derived from genetic association studies on adult adiposity were also associated with birth weight and child adiposity, indicating an overlap between the genetic pathways influencing metabolic health in early and later life. Neonatal methylation markers from seven gene loci (ANK3, CDKN2B, CACNA1G, IGDCC4, P4HA3, ZNF423 and MIRLET7BHG) were significantly associated with birth weight, with a subset of these in genes previously implicated in metabolic pathways in humans and in animal models. Methylation levels at three of seven birth weight-linked loci showed significant association with prenatal environment, but none were affected by polygenic risk score. Six of these birth weight-linked loci continued to show a longitudinal association with offspring size and/or adiposity in early childhood.

Conclusions: This study provides further evidence that developmental pathways to adiposity begin before birth and are influenced by environmental, genetic and epigenetic factors. These pathways can have a lasting effect on offspring size, adiposity and future metabolic outcomes, and offer new opportunities for risk stratification and prevention of obesity.

Clinical Trial Registration: This birth cohort is a prospective observational study, designed to study the developmental origins of health and disease, and was retrospectively registered on 1 July 2010 under the identifier NCT01174875 .

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http://dx.doi.org/10.1186/s12916-017-0800-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340003PMC
March 2017
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