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Interplay between polymorphisms and methylation in the H19/IGF2 gene region may contribute to obesity in Mexican-American children

Published online by Cambridge University Press:  20 September 2013

M. A. Hernández-Valero
Affiliation:
Department of Health Disparities Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
J. Rother
Affiliation:
Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
I. Gorlov
Affiliation:
Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, NH, USA
M. Frazier
Affiliation:
Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
O. Gorlova*
Affiliation:
Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, NH, USA
*
*Address for correspondence: O. Gorlova, Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, One Medical Center Dr, Lebanon, NH 03756. (Email [email protected])

Abstract

Imprinted genes often affect body size-related traits such as weight. However, the association of imprinting with obesity, especially childhood obesity, has not been well studied. Mexican-American children have a high prevalence, approaching 50%, of obesity and/or overweight. In a pilot study of 75 Mexican-American children, we analyzed the relationships among obese/overweight status, methylation status and single-nucleotide polymorphism (SNP) status at a CpG site in a differentially methylated region (DMR) of the imprinted H19/IGF2 locus. We observed a significant difference in SNP rs10732516 frequency between boys and girls among the overweight and obese children but not among the lean children. We also found that children with lower methylation of the polymorphic CpG site (CpG4) in the H19 DMR had higher birth weights than did children with higher methylation (P = 0.04). Our results suggest that CpG4 methylation status may be associated with childhood obesity in Mexican-American children in a sex-specific manner.

Type
Original Article
Copyright
Copyright © Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2013 

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References

1.Ogden, CL, Carroll, MD, Flegal, KM. High body mass index for age among US children and adolescents, 2003–2006. JAMA. 2008; 299, 24012405.Google Scholar
2.Freedman, DS, Kahn, HS, Mei, Z, Grummer-Strawn, LM, Dietz, WH, Srinivasan, SR, et al. Relation of body mass index and waist-to-height ratio to cardiovascular disease risk factors in children and adolescents: the Bogalusa Heart Study. Am J Clin Nutr. 2007; 86, 3340.CrossRefGoogle ScholarPubMed
3.Freedman, DS, Khan, LK, Dietz, WH, Srinivasan, SR, Berenson, GS. Relationship of childhood obesity to coronary heart disease risk factors in adulthood: the Bogalusa Heart Study. Pediatrics. 2001; 108, 712718.Google Scholar
4.Serdula, MK, Ivery, D, Coates, RJ, Freedman, DS, Williamson, DF, Byers, T. Do obese children become obese adults? A review of the literature. Prev Med. 1993; 22, 167177.Google Scholar
5.Whitaker, RC, Wright, JA, Pepe, MS, Seidel, KD, Dietz, WH. Predicting obesity in young adulthood from childhood and parental obesity. N Engl J Med. 1997; 337, 869873.Google Scholar
6.Hernández-Valero, MA, Bustamante-Montes, LP, Hernandez, M, Halley-Castillo, E, Wilkinson, AV, Bondy, ML, et al. Higher risk for obesity among Mexican-American and Mexican immigrant children and adolescents than among peers in Mexico. J Immigr Minor Health. 2012; 14, 517522.Google Scholar
7.Bartolomei, MS, Tilghman, SM. Genomic imprinting in mammals. Annu Rev Genet. 1997; 31, 493525.Google Scholar
8.Gorlova, OY, Amos, CI, Wang, NW, Shete, S, Turner, ST, Boerwinkle, E. Genetic linkage and imprinting effects on body mass index in children and young adults. Eur J Hum Genet. 2003; 11, 425432.Google Scholar
9.Cassidy, SB, Driscoll, DJ. Prader-Willi syndrome. Eur J Hum Genet. 2009; 17, 313.CrossRefGoogle ScholarPubMed
10.Mahgoub, NA. Prader-Willi syndrome. J Neuropsychiatry Clin Neurosci. 2007; 19, 203204.Google Scholar
11.Freson, K, Thys, C, Wittevrongel, C, Proesmans, W, Hoylaerts, MF, Vermylen, J, et al. Pseudohypoparathyroidism type Ib with disturbed imprinting in the GNAS1 cluster and Gsalpha deficiency in platelets. Hum Mol Genet. 2002; 11, 27412750.Google Scholar
12.Liu, J, Litman, D, Rosenberg, MJ, Yu, S, Biesecker, LG, Weinstein, LS. A GNAS1 imprinting defect in pseudohypoparathyroidism type IB. J Clin Invest. 2000; 106, 11671174.Google Scholar
13.Gorlova, OY, Lei, L, Zhu, D, Weng, SF, Shete, S, Zhang, Y, et al. Imprinting detection by extending a regression-based QTL analysis method. Hum Genet. 2007; 122, 159174.Google Scholar
14.Guo, YF, Shen, H, Liu, YJ, Wang, W, Xiong, DH, Xiao, P, et al. Assessment of genetic linkage and parent-of-origin effects on obesity. J Clin Endocrinol Metab. 2006; 91, 40014005.Google Scholar
15.Roth, SM, Schrager, MA, Metter, EJ, Riechman, SE, Fleg, JL, Hurley, BF, et al. IGF2 genotype and obesity in men and women across the adult age span. Int J Obes Relat Metab Disord. 2002; 26, 585587.CrossRefGoogle ScholarPubMed
16.Martin, RM, Holly, JM, Davey Smith, G, Gunnell, D. Associations of adiposity from childhood into adulthood with insulin resistance and the insulin-like growth factor system: 65-year follow-up of the Boyd Orr Cohort. J Clin Endocrinol Metab. 2006; 91, 32873295.CrossRefGoogle ScholarPubMed
17.Heijmans, BT, Kremer, D, Tobi, EW, Boomsma, DI, Slagboom, PE. Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus. Hum Mol Genet. 2007; 16, 547554.Google Scholar
18.Perkins, E, Murphy, SK, Murtha, AP, Schildkraut, J, Jirtle, RL, Demark-Wahnefried, W, et al. Insulin-like growth factor 2/H19 methylation at birth and risk of overweight and obesity in children. J Pediatr. 2012; 161, 3139.CrossRefGoogle ScholarPubMed
19.Hernández-Valero, MA, Herrera, AP, Zahm, SH, Jones, LA. Community-based participatory research and gene-environment interaction methodologies addressing environmental justice among migrant and seasonal farm worker women and children in Texas: “From Mother to Child Project”. Californian Journal of Health Promotion. 2007; 5(Sp Iss (Hlth Disp & Soc Justice)), 114127.Google Scholar
20.Hammer, LD, Kraemer, HC, Wilson, DM, Ritter, PL, Dornbusch, SM. Standardized percentile curves of body-mass index for children and adolescents. Am J Dis Child. 1991; 145, 259263.Google Scholar
21.Takai, D, Gonzales, FA, Tsai, YC, Thayer, MJ, Jones, PA. Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer. Hum Mol Genet. 2001; 10, 26192626.Google Scholar
22.Seki, Y, Williams, L, Vuguin, PM, Charron, MJ. Minireview: epigenetic programming of diabetes and obesity: animal models. Endocrinology. 2012; 153, 10311038.Google Scholar
23.Simmons, R. Epigenetics and maternal nutrition: nature v nurture. Proc Nutr Soc. 2011; 70, 7381.Google Scholar
24.Campion, J, Milagro, F, Martinez, JA. Epigenetics and obesity. Prog Mol Biol Transl Sci. 2010; 94, 291347.CrossRefGoogle ScholarPubMed
25.Lavebratt, C, Almgren, M, Ekstrom, TJ. Epigenetic regulation in obesity. Int J Obes. 2012; 36, 757765.Google Scholar
26.Lillycrop, KA, Burdge, GC. Epigenetic changes in early life and future risk of obesity. Int J Obes. 2011; 35, 7283.Google Scholar
27.Pinnick, KE, Karpe, F. DNA methylation of genes in adipose tissue. Proc Nutr Soc. 2011; 70, 5763.Google Scholar
28.Hodgkinson, A, Eyre-Walker, A. Variation in the mutation rate across mammalian genomes. Nature Rev Genet. 2011; 12, 756766.Google Scholar
29.Murphy, SK, Huang, Z, Hoyo, C. Differentially methylated regions of imprinted genes in prenatal, perinatal and postnatal human tissues. PLoS One. 2012; 7, e40924.CrossRefGoogle ScholarPubMed
30.Huang, RC, Galati, JC, Burrows, S, Beilin, LJ, Li, X, Pennell, CE, et al. DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults. Clin Epigenetics. 2012; 4, 21.Google Scholar
31.Burris, HH, Braun, JM, Byun, HM, Tarantini, L, Mercado, A, Wright, RJ, et al. Association between birth weight and DNA methylation of IGF2, glucocorticoid receptor and repetitive elements LINE-1 and Alu. Epigenomics. 2013; 5, 271281.Google Scholar
32.Hackett, JA, Surani, MA. DNA methylation dynamics during the mammalian life cycle. Philos Trans R Soc Lond B Biol Sci. 2013; 368, 20110328.CrossRefGoogle ScholarPubMed
33.Maegawa, S, Hinkal, G, Kim, HS, Shen, L, Zhang, L, Zhang, J, et al. Widespread and tissue specific age-related DNA methylation changes in mice. Genome Res. 2010; 20, 332340.Google Scholar
34.Teschendorff, AE, Menon, U, Gentry-Maharaj, A, Ramus, SJ, Weisenberger, DJ, Shen, H, et al. Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer. Genome Res. 2010; 20, 440446.Google Scholar
35.Murphy, SK, Huang, Z, Hoyo, C. Differentially methylated regions of imprinted genes in prenatal, perinatal and postnatal human tissues. PLoS One. 2012; 7(7), e40924.Google Scholar
36.Bick, J, Naumova, O, Hunter, S, Barbot, B, Lee, M, Luthar, SS, et al. Childhood adversity and DNA methylation of genes involved in the hypothalamus–pituitary–adrenal axis and immune system: whole-genome and candidate-gene associations. Dev Psychopathol. 2012; 24, 14171425.Google Scholar
37.Yang, BZ, Zhang, H, Ge, W, Weder, N, Douglas-Palumberi, H, Perepletchikova, F, et al. Child abuse and epigenetic mechanisms of disease risk. Am J Prev Med. 2013; 44, 101107.Google Scholar
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