Abstract
Access to nutrition in the perinatal stage or early childhood has pronounced influence on later development and health outcomes in adolescence and adulthood. Total energy intake and a variety of dietary components, such as protein, folate, choline, curcumin, and polyphenols consumed in early life, have been shown to modify indicators of chronic diseases such as obesity, diabetes, and cardiovascular disease. These dietary components interact with epigenetic regulation. By altering DNA methylation and histone modifications, dietary exposures in early life affect the transcription of genes related to somatic growth, appetite control, stress response, and adiposity which precedes various chronic diseases. This chapter will introduce the existing human and animal evidence which supports the interaction between nutrition and epigenetics in early life and its lasting impacts on health and development.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Aiken, C. E., & Ozanne, S. E. (2013). Sex differences in developmental programming models. Reproduction, 145, R1–R13.
Altobelli, G., Bogdarina, I. G., Stupka, E., Clark, A. J., & Langley-Evans, S. (2013). Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acid. PLoS One, 8, e82989.
Baker, J. L., Olsen, L. W., & Sørensen, T. I. (2008). Weight at birth and all-cause mortality in adulthood. Epidemiology, 19, 197–203.
Barker, D. J., & Osmond, C. (1988). Low birth weight and hypertension. BMJ, 297, 134–135.
Barker, D. J., Winter, P. D., Osmond, C., Margetts, B., & Simmonds, S. J. (1989). Weight in infancy and death from ischaemic heart disease. Lancet, 2, 577–580.
Bateson, P., Barker, D., Clutton-Brock, T., Deb, D., D'Udine, B., Foley, R. A., et al. (2004). Developmental plasticity and human health. Nature, 430, 419–421.
Begum, G., Davies, A., Stevens, A., Oliver, M., Jaquiery, A., Challis, J., et al. (2013). Maternal undernutrition programs tissue-specific epigenetic changes in the glucocorticoid receptor in adult offspring. Endocrinology, 154, 4560–4569.
Bertolo, R. F., & McBreairty, L. E. (2013). The nutritional burden of methylation reactions. Current Opinion in Clinical Nutrition and Metabolic Care, 16, 102–108.
Boeke, C. E., Gillman, M. W., Hughes, M. D., Rifas-Shiman, S. L., Villamor, E., & Oken, E. (2013). Choline intake during pregnancy and child cognition at age 7 years. American Journal of Epidemiology, 177, 1338–1347.
Brameld, J. M., Mostyn, A., Dandrea, J., Stephenson, T. J., Dawson, J. M., Buttery, P. J., et al. (2000). Maternal nutrition alters the expression of insulin-like growth factors in fetal sheep liver and skeletal muscle. The Journal of Endocrinology, 167, 429–437.
Brandeis, M., Kafri, T., Ariel, M., Chaillet, J. R., McCarrey, J., Razin, A., et al. (1993). The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. The EMBO Journal, 12, 3669–3677.
Brenseke, B., Prater, M. R., Bahamonde, J., & Gutierrez, J. C. (2013). Current thoughts on maternal nutrition and fetal programming of the metabolic syndrome. Journal of Pregnancy, 2013, 368461.
Burdge, G. C., & Lillycrop, K. A. (2010). Nutrition, epigenetics, and developmental plasticity: Implications for understanding human disease. Annual Review of Nutrition, 30, 315–339.
Carmody, J. S., Wan, P., Accili, D., Zeltser, L. M., & Leibel, R. L. (2011). Respective contributions of maternal insulin resistance and diet to metabolic and hypothalamic phenotypes of progeny. Obesity (Silver Spring), 19, 492–499.
Chen, J. H., Martin-Gronert, M. S., Tarry-Adkins, J., & Ozanne, S. E. (2009). Maternal protein restriction affects postnatal growth and the expression of key proteins involved in lifespan regulation in mice. PLoS One, 4, e4950.
Choi, S. W., & Friso, S. (2010). Epigenetics: A new bridge between nutrition and health. Advances in Nutrition, 1, 8–16.
Davison, J. M., Mellott, T. J., Kovacheva, V. P., & Blusztajn, J. K. (2009). Gestational choline supply regulates methylation of histone H3, expression of histone methyltransferases G9a (Kmt1c) and Suv39h1 (Kmt1a), and DNA methylation of their genes in rat fetal liver and brain. The Journal of Biological Chemistry, 284, 1982–1989.
DeChiara, T. M., Efstratiadis, A., & Robertson, E. J. (1990). A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature, 345, 78–80.
Delage, B., & Dashwood, R. H. (2008). Dietary manipulation of histone structure and function. Annual Review of Nutrition, 28, 347–366.
Drake, A. J., McPherson, R. C., Godfrey, K. M., Cooper, C., Lillycrop, K. A., Hanson, M. A., et al. (2012). An unbalanced maternal diet in pregnancy associates with offspring epigenetic changes in genes controlling glucocorticoid action and foetal growth. Clinical Endocrinology, 77, 808–815.
Fernandez-Twinn, D. S., & Ozanne, S. E. (2006). Mechanisms by which poor early growth programs type-2 diabetes, obesity and the metabolic syndrome. Physiology and Behavior, 88, 234–243.
Gilbert, E. R., & Liu, D. (2010). Flavonoids influence epigenetic-modifying enzyme activity: Structure – function relationships and the therapeutic potential for cancer. Current Medicinal Chemistry, 17, 1756–1768.
Gillman, M. W., Rifas-Shiman, S., Berkey, C. S., Field, A. E., & Colditz, G. A. (2003). Maternal gestational diabetes, birth weight, and adolescent obesity. Pediatrics, 111, e221–e226.
Gong, L., Pan, Y. X., & Chen, H. (2010). Gestational low protein diet in the rat mediates Igf2 gene expression in male offspring via altered hepatic DNA methylation. Epigenetics, 5, 619–626.
Grygiel-Górniak, B. (2014). Peroxisome proliferator-activated receptors and their ligands: Nutritional and clinical implications—a review. Nutrition Journal, 13, 17.
Hales, C. N., & Barker, D. J. (1992). Type 2 (non-insulin-dependent) diabetes mellitus: The thrifty phenotype hypothesis. Diabetologia, 35, 595–601.
Heijmans, B. T., Tobi, E. W., Stein, A. D., Putter, H., Blauw, G. J., Susser, E. S., et al. (2008). Persistent epigenetic differences associated with prenatal exposure to famine in humans. Proceedings of the National Academy of Sciences of the United States of America, 105, 17046–17049.
Herrick, K., Phillips, D. I., Haselden, S., Shiell, A. W., Campbell-Brown, M., & Godfrey, K. M. (2003). Maternal consumption of a high-meat, low-carbohydrate diet in late pregnancy: Relation to adult cortisol concentrations in the offspring. The Journal of Clinical Endocrinology and Metabolism, 88, 3554–3560.
Hochberg, Z., Feil, R., Constancia, M., Fraga, M., Junien, C., Carel, J. C., et al. (2011). Child health, developmental plasticity, and epigenetic programming. Endocrine Reviews, 32, 159–224.
Hoyo, C., Murtha, A. P., Schildkraut, J. M., Jirtle, R. L., Demark-Wahnefried, W., Forman, M. R., et al. (2011). Methylation variation at IGF2 differentially methylated regions and maternal folic acid use before and during pregnancy. Epigenetics, 6, 928–936.
Huang, R. C., Galati, J. C., Burrows, S., Beilin, L. J., Li, X., Pennell, C. E., et al. (2012). DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults. Clinical Epigenetics, 4, 21.
Hult, M., Tornhammar, P., Ueda, P., Chima, C., Bonamy, A. K., Ozumba, B., et al. (2010). Hypertension, diabetes and overweight: Looming legacies of the Biafran famine. PLoS One, 5, e13582.
Illingworth, R. S., & Bird, A. P. (2009). CpG islands—‘A rough guide’. FEBS Letters, 583, 1713–1720.
Institute of Medicine. (1998). Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin and choline. Washington, DC: National Academy Press.
Jiang, X., Yan, J., West, A. A., Perry, C. A., Malysheva, O. V., Devapatla, S., et al. (2012). Maternal choline intake alters the epigenetic state of fetal cortisol-regulating genes in humans. The FASEB Journal, 26, 3563–3574.
Jirtle, R. L., & Skinner, M. K. (2007). Environmental epigenomics and disease susceptibility. Nature Reviews Genetics, 8, 253–262.
Jones, B. K., Levorse, J., & Tilghman, S. M. (2001). Deletion of a nuclease-sensitive region between the Igf2 and H19 genes leads to Igf2 misregulation and increased adiposity. Human Molecular Genetics, 10, 807–814.
Jousse, C., Parry, L., Lambert-Langlais, S., Maurin, A. C., Averous, J., Bruhat, A., et al. (2011). Perinatal undernutrition affects the methylation and expression of the leptin gene in adults: implication for the understanding of metabolic syndrome. The FASEB Journal, 25, 3271–3278.
Korosi, A., & Baram, T. Z. (2010). Plasticity of the stress response early in life: Mechanisms and significance. Developmental Psychobiology, 52, 661–670.
Kovacheva, V. P., Davison, J. M., Mellott, T. J., Rogers, A. E., Yang, S., O’Brien, M. J., et al. (2009). Raising gestational choline intake alters gene expression in DMBA-evoked mammary tumors and prolongs survival. The FASEB Journal, 23, 1054–1063.
Kovacheva, V. P., Mellott, T. J., Davison, J. M., Wagner, N., Lopez-Coviella, I., Schnitzler, A. C., et al. (2007). Gestational choline deficiency causes global and Igf2 gene DNA hypermethylation by up-regulation of Dnmt1 expression. The Journal of Biological Chemistry, 282, 31777–31788.
Levitt, N. S., Lindsay, R. S., Holmes, M. C., & Seckl, J. R. (1996). Dexamethasone in the last week of pregnancy attenuates hippocampal glucocorticoid receptor gene expression and elevates blood pressure in the adult offspring in the rat. Neuroendocrinology, 64, 412–418.
Li, Y., Jaddoe, V. W., Qi, L., He, Y., Wang, D., Lai, J., et al. (2011a). Exposure to the Chinese famine in early life and the risk of metabolic syndrome in adulthood. Diabetes Care, 34, 1014–1018.
Li, M., Sloboda, D. M., & Vickers, M. H. (2011b). Maternal obesity and developmental programming of metabolic disorders in offspring: Evidence from animal models. Experimental Diabetes Research, 2011, 592408.
Li, Y., & Tollefsbol, T. O. (2010). Impact on DNA methylation in cancer prevention and therapy by bioactive dietary components. Current Medicinal Chemistry, 17, 2141–2151.
Liberato, S. C., Singh, G., & Mulholland, K. (2013). Effects of protein energy supplementation during pregnancy on fetal growth: A review of the literature focusing on contextual factors. Food and Nutrition Research 57. doi: 10.3402/fnr.v57i0.20499. eCollection 2013.
Lillycrop, K. A., Phillips, E. S., Jackson, A. A., Hanson, M. A., & Burdge, G. C. (2005). Dietary protein restriction of pregnant rats induces and folic acid supplementation prevents epigenetic modification of hepatic gene expression in the offspring. Journal of Nutrition, 135, 1382–1386.
Liu, D., Diorio, J., Tannenbaum, B., Caldji, C., Francis, D., Freedman, A., et al. (1997). Maternal care, hippocampal glucocorticoid receptors, and hypothalamic-pituitary-adrenal responses to stress. Science, 277, 1659–1662.
Lucassen, P. J., Naninck, E. F., van Goudoever, J. B., Fitzsimons, C., Joels, M., & Korosi, A. (2013). Perinatal programming of adult hippocampal structure and function; emerging roles of stress, nutrition and epigenetics. Trends in Neurosciences, 36, 621–631.
Lui, J. C., Finkielstain, G. P., Barnes, K. M., & Baron, J. (2008). An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, 295, R189–R196.
Magliano, D. C., Bargut, T. C., de Carvalho, S. N., Aguila, M. B., Mandarim-de-Lacerda, C. A., & Souza-Mello, V. (2013). Peroxisome proliferator-activated receptors-alpha and gamma are targets to treat offspring from maternal diet-induced obesity in mice. PLoS One, 8, e64258.
Maloney, C. A., Hay, S. M., Young, L. E., Sinclair, K. D., & Rees, W. D. (2011). A methyl-deficient diet fed to rat dams during the peri-conception period programs glucose homeostasis in adult male but not female offspring. The Journal of Nutrition, 141, 95–100.
Mao, J., Zhang, X., Sieli, P. T., Falduto, M. T., Torres, K. E., & Rosenfeld, C. S. (2010). Contrasting effects of different maternal diets on sexually dimorphic gene expression in the murine placenta. Proceedings of the National Academy of Sciences of the United States of America, 107, 5557–5562.
Marco, A., Kisliouk, T., Weller, A., & Meiri, N. (2013). High fat diet induces hypermethylation of the hypothalamic Pomc promoter and obesity in post-weaning rats. Psychoneuroendocrinology, 38, 2844–2853.
Mayer, W., Niveleau, A., Walter, J., Fundele, R., & Haaf, T. (2000). Demethylation of the zygotic paternal genome. Nature, 403, 501–502.
McCann, J. C., Hudes, M., & Ames, B. N. (2006). An overview of evidence for a causal relationship between dietary availability of choline during development and cognitive function in offspring. Neuroscience and Biobehavioral Reviews, 30, 696–712.
McCurdy, C. E., Bishop, J. M., Williams, S. M., Grayson, B. E., Smith, M. S., Friedman, J. E., et al. (2009). Maternal high-fat diet triggers lipotoxicity in the fetal livers of nonhuman primates. The Journal of Clinical Investigation, 119, 323–335.
Meaney, M. J., & Szyf, M. (2005). Environmental programming of stress responses through DNA methylation: Life at the interface between a dynamic environment and a fixed genome. Dialogues in Clinical Neuroscience, 7, 103–123.
Mehedint, M. G., Craciunescu, C. N., & Zeisel, S. H. (2010a). Maternal dietary choline deficiency alters angiogenesis in fetal mouse hippocampus. Proceedings of the National Academy of Sciences of the United States of America, 107, 12834–12839.
Mehedint, M. G., Niculescu, M. D., Craciunescu, C. N., & Zeisel, S. H. (2010b). Choline deficiency alters global histone methylation and epigenetic marking at the Re1 site of the calbindin 1 gene. The FASEB Journal, 24, 184–195.
Mills, J. L., Fan, R., Brody, L. C., Liu, A., Ueland, P. M., Wang, Y., et al. (2014). Maternal choline concentrations during pregnancy and choline-related genetic variants as risk factors for neural tube defects. American Journal of Clinical Nutrition, 100, 1069–1074.
Miñana-Solis, M. D. C., & Escobar, C. (2008). Post-weaning protein malnutrition in the rat produces short and long term metabolic impairment, in contrast to earlier and later periods. International Journal of Biological Sciences, 4, 422–432.
Morison, I. M., Paton, C. J., & Cleverley, S. D. (2001). The imprinted gene and parent-of-origin effect database. Nucleic Acids Research, 29, 275–276.
Morris, M. J., & Chen, H. (2009). Established maternal obesity in the rat reprograms hypothalamic appetite regulators and leptin signaling at birth. International Journal of Obesity, 33, 115–122.
Mortensen, O. H., Olsen, H. L., Frandsen, L., Nielsen, P. E., Nielsen, F. C., Grunnet, N., et al. (2010). Gestational protein restriction in mice has pronounced effects on gene expression in newborn offspring’s liver and skeletal muscle; protective effect of taurine. Pediatric Research, 67, 47–53.
Naess, O., Stoltenberg, C., Hoff, D. A., Nystad, W., Magnus, P., Tverdal, A., et al. (2013). Cardiovascular mortality in relation to birth weight of children and grandchildren in 500,000 Norwegian families. European Heart Journal, 34, 3427–3436.
O’Donnell, K., O'Connor, T. G., & Glover, V. (2009). Prenatal stress and neurodevelopment of the child: Focus on the HPA axis and role of the placenta. Developmental Neuroscience, 31, 285–292.
Ogawa, T., Shibato, J., Rakwal, R., Saito, T., Tamura, G., Kuwagata, M., et al. (2014). Seeking genes responsible for developmental origins of health and disease from the fetal mouse liver following maternal food restriction. Congenital Anomalies (Kyoto), 54, 195–219.
Ong, K. K., Ahmed, M. L., Emmett, P. M., Preece, M. A., & Dunger, D. B. (2000). Association between postnatal catch-up growth and obesity in childhood: Prospective cohort study. BMJ, 320, 967–971.
Ooi, S. K., O’Donnell, A. H., & Bestor, T. H. (2009). Mammalian cytosine methylation at a glance. Journal of Cell Science, 122, 2787–2791.
Ooi, S. K., Qiu, C., Bernstein, E., Li, K., Jia, D., Yang, Z., et al. (2007). DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA. Nature, 448, 714–717.
Palou, M., Priego, T., Sánchez, J., Palou, A., & Picó, C. (2013). Metabolic programming of sirtuin 1 (SIRT1) expression by moderate energy restriction during gestation in rats may be related to obesity susceptibility in later life. The British Journal of Nutrition, 109, 757–764.
Patel, M. S., & Srinivasan, M. (2011). Metabolic programming in the immediate postnatal life. Annals of Nutrition and Metabolism, 58(Suppl 2), 18–28.
Perkins, E., Murphy, S. K., Murtha, A. P., Schildkraut, J., Jirtle, R. L., Demark-Wahnefried, W., et al. (2012). Insulin-like growth factor 2/H19 methylation at birth and risk of overweight and obesity in children. The Journal of Pediatrics, 161, 31–39.
Rich-Edwards, J. W., Stampfer, M. J., Manson, J. E., Rosner, B., Hankinson, S. E., Colditz, G. A., et al. (1997). Birth weight and risk of cardiovascular disease in a cohort of women followed up since 1976. BMJ, 315, 396–400.
Roseboom, T., de Rooij, S., & Painter, R. (2006). The Dutch famine and its long-term consequences for adult health. Early Human Development, 82, 485–491.
Roseboom, T. J., Painter, R. C., van Abeelen, A. F., Veenendaal, M. V., & de Rooij, S. R. (2011). Hungry in the womb: What are the consequences? Lessons from the Dutch famine. Maturitas, 70, 141–145.
Ross, R. G., Hunter, S. K., McCarthy, L., Beuler, J., Hutchison, A. K., Wagner, B. D., et al. (2013). Perinatal choline effects on neonatal pathophysiology related to later schizophrenia risk. The American Journal of Psychiatry, 170, 290–298.
Sampey, B. P., Vanhoose, A. M., Winfield, H. M., Freemerman, A. J., Muehlbauer, M. J., Fueger, P. T., et al. (2011). Cafeteria diet is a robust model of human metabolic syndrome with liver and adipose inflammation: Comparison to high-fat diet. Obesity (Silver Spring), 19, 1109–1117.
Sarr, O., Yang, K., & Regnault, T. R. (2012). In utero programming of later adiposity: The role of fetal growth restriction. Journal of Pregnancy, 2012, 134758.
Schemies, J., Uciechowska, U., Sippl, W., & Jung, M. (2010). NAD(+) -dependent histone deacetylases (sirtuins) as novel therapeutic targets. Medicinal Research Reviews, 30, 861–889.
Shaw, G. M., Finnell, R. H., Blom, H. J., Carmichael, S. L., Vollset, S. E., Yang, W., et al. (2009). Choline and risk of neural tube defects in a folate-fortified population. Epidemiology, 20, 714–719.
Shiell, A. W., Campbell-Brown, M., Haselden, S., Robinson, S., Godfrey, K. M., & Barker, D. J. (2001). High-meat, low-carbohydrate diet in pregnancy: Relation to adult blood pressure in the offspring. Hypertension, 38, 1282–1288.
Sinclair, K. D., Allegrucci, C., Singh, R., Gardner, D. S., Sebastian, S., Bispham, J., et al. (2007). DNA methylation, insulin resistance, and blood pressure in offspring determined by maternal periconceptional B vitamin and methionine status. Proceedings of the National Academy of Sciences of the United States of America, 104, 19351–19356.
Smith, S. M., & Vale, W. W. (2006). The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress. Dialogues in Clinical Neuroscience, 8, 383–395.
Steegers-Theunissen, R. P., Obermann-Borst, S. A., Kremer, D., Lindemans, J., Siebel, C., Steegers, E. A., et al. (2009). Periconceptional maternal folic acid use of 400 microg per day is related to increased methylation of the IGF2 gene in the very young child. PLoS One, 4, e7845.
Steiger, H., Labonté, B., Groleau, P., Turecki, G., & Israel, M. (2013). Methylation of the glucocorticoid receptor gene promoter in bulimic women: Associations with borderline personality disorder, suicidality, and exposure to childhood abuse. International Journal of Eating Disorders, 46, 246–255.
Stein, A. D., Barnhart, H. X., Hickey, M., Ramakrishnan, U., Schroeder, D. G., & Martorell, R. (2003). Prospective study of protein-energy supplementation early in life and of growth in the subsequent generation in Guatemala. The American Journal of Clinical Nutrition, 78, 162–167.
Stuart, A., Amer-Wåhlin, I., Persson, J., & Källen, K. (2013). Long-term cardiovascular risk in relation to birth weight and exposure to maternal diabetes mellitus. International Journal of Cardiology, 168, 2653–2657.
Susser, E., Kirkbride, J. B., Heijmans, B. T., Kresovich, J. K., Lumey, L. H., & Stein, A. D. (2012). Maternal prenatal nutrition and health in grandchildren and subsequent generations. Annual Review of Anthropology, 41, 577–610.
Talens, R. P., Boomsma, D. I., Tobi, E. W., Kremer, D., Jukema, J. W., Willemsen, G., et al. (2010). Variation, patterns, and temporal stability of DNA methylation: Considerations for epigenetic epidemiology. The FASEB Journal, 24, 3135–3144.
Thompson, M. D., Cole, D. E., & Ray, J. G. (2009). Vitamin B-12 and neural tube defects: The Canadian experience. The American Journal of Clinical Nutrition, 89, 697S–701S.
Tobi, E. W., Goeman, J. J., Monajemi, R., Gu, H., Putter, H., Zhang, Y., et al. (2014). DNA methylation signatures link prenatal famine exposure to growth and metabolism. Nature Communications, 5, 5592.
Tobi, E. W., Lumey, L. H., Talens, R. P., Kremer, D., Putter, H., Stein, A. D., et al. (2009). DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific. Human Molecular Genetics, 18, 4046–4053.
Tobi, E. W., Slagboom, P. E., van Dongen, J., Kremer, D., Stein, A. D., Putter, H., et al. (2012). Prenatal famine and genetic variation are independently and additively associated with DNA methylation at regulatory loci within IGF2/H19. PLoS One, 7, e37933.
Tsai, H. W., Grant, P. A., & Rissman, E. F. (2009). Sex differences in histone modifications in the neonatal mouse brain. Epigenetics, 4, 47–53.
Vogt, M. C., Paeger, L., Hess, S., Steculorum, S. M., Awazawa, M., Hampel, B., et al. (2014). Neonatal insulin action impairs hypothalamic neurocircuit formation in response to maternal high-fat feeding. Cell, 156, 495–509.
Vohr, B. R., McGarvey, S. T., & Tucker, R. (1999). Effects of maternal gestational diabetes on offspring adiposity at 4–7 years of age. Diabetes Care, 22, 1284–1291.
Voigt, P., Tee, W. W., & Reinberg, D. (2013). A double take on bivalent promoters. Genes and Development, 27, 1318–1338.
Vucetic, Z., Kimmel, J., Totoki, K., Hollenbeck, E., & Reyes, T. M. (2010). Maternal high-fat diet alters methylation and gene expression of dopamine and opioid-related genes. Endocrinology, 151, 4756–4764.
Waterland, R. A., Dolinoy, D. C., Lin, J. R., Smith, C. A., Shi, X., & Tahiliani, K. G. (2006). Maternal methyl supplements increase offspring DNA methylation at Axin fused. Genesis, 44, 401–406.
Waterland, R. A., & Jirtle, R. L. (2003). Transposable elements: Targets for early nutritional effects on epigenetic gene regulation. Molecular and Cellular Biology, 23, 5293–5300.
Waterland, R. A., Travisano, M., Tahiliani, K. G., Rached, M. T., & Mirza, S. (2008). Methyl donor supplementation prevents transgenerational amplification of obesity. International Journal of Obesity, 32, 1373–1379.
Williams-Wyss, O., Zhang, S., MacLaughlin, S. M., Kleemann, D., Walker, S. K., Suter, C. M., et al. (2014). Embryo number and periconceptional undernutrition in the sheep have differential effects on adrenal epigenotype, growth, and development. The American Journal of Physiology: Endocrinology and Metabolism, 307, E141–E150.
Winick, M., & Noble, A. (1966). Cellular response in rats during malnutrition at various ages. Journal of Nutrition, 89, 300–306.
Woodall, S. M., Johnston, B. M., Breier, B. H., & Gluckman, P. D. (1996). Chronic maternal undernutrition in the rat leads to delayed postnatal growth and elevated blood pressure of offspring. Pediatric Research, 40, 438–443.
Yang, T., Fu, M., Pestell, R., & Sauve, A. A. (2006). SIRT1 and endocrine signaling. Trends in Endocrinology and Metabolism, 17, 186–191.
Yokomizo, H., Inoguchi, T., Sonoda, N., Sakaki, Y., Maeda, Y., Inoue, T., et al. (2014). Maternal high-fat diet induces insulin resistance and deterioration of pancreatic β-cell function in adult offspring with sex differences in mice. The American Journal of Physiology: Endocrinology and Metabolism, 306, E1163–E1175.
Zhang, S., Rattanatray, L., MacLaughlin, S. M., Cropley, J. E., Suter, C. M., Molloy, L., et al. (2010). Periconceptional undernutrition in normal and overweight ewes leads to increased adrenal growth and epigenetic changes in adrenal IGF2/H19 gene in offspring. The FASEB Journal, 24, 2772–2782.
Zheng, X., Wang, Y., Ren, W., Luo, R., Zhang, S., Zhang, J. H., et al. (2012). Risk of metabolic syndrome in adults exposed to the great Chinese famine during the fetal life and early childhood. European Journal of Clinical Nutrition, 66, 231–236.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Abbreviations
Abbreviations
- ACTH:
-
Adrenocorticotropic hormone
- AgRP:
-
Agouti-related peptide
- BHMT:
-
Betaine homocysteine methyltransferase
- CpG:
-
Cytosine-guanine dinucleotide
- CPT1A:
-
Carnitine palmitoyltransferase-1A
- CRH:
-
Corticotropin-releasing hormone
- CTCF:
-
CCCTC-binding factor
- DNMT:
-
DNA methyltransferase
- GR:
-
Glucocorticoid receptor
- HAT:
-
Histone acetyltransferase
- HDAC:
-
Histone deacetylase
- HMT:
-
Histone methyltransferase
- HPA axis:
-
The hypothalamic-pituitary-adrenal axis
- IGF2:
-
Insulin growth-like factor 2
- INSR:
-
Insulin receptor
- LDL:
-
Low-density lipoprotein
- 5-CH3-THF:
-
Methyltetrahydrofolate
- NTD:
-
Neural tube defect
- PCK1:
-
Phosphoenolpyruvate carboxykinase
- POMC:
-
Pro-opiomelanocortin
- PPAR:
-
Peroxisome proliferator-activated receptors
- SAM:
-
S-adenosylmethionine
Rights and permissions
Copyright information
© 2016 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Jiang, X. (2016). Nutrition in Early Life, Epigenetics, and Health. In: Hollar, D. (eds) Epigenetics, the Environment, and Children’s Health Across Lifespans. Springer, Cham. https://doi.org/10.1007/978-3-319-25325-1_6
Download citation
DOI: https://doi.org/10.1007/978-3-319-25325-1_6
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-25323-7
Online ISBN: 978-3-319-25325-1
eBook Packages: MedicineMedicine (R0)