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Research Article

Combined influence of gene-specific cord blood methylation and maternal smoking habit on birth weight

    Kim E Haworth

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK

    ,
    William E Farrell

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK

    ,
    Richard D Emes

    School of Veterinary Medicine & Science, University of Nottingham, Sutton Bonington Campus, Sutton Bonington, Leicestershire, UK

    ,
    Khaled MK Ismail

    School of Clinical & Experimental Medicine, College of Medical & Dental Sciences, University of Birmingham, Birmingham, UK and Birmingham Women’s NHS Foundation Trust, Edgbaston, Birmingham UK

    ,
    William D Carroll

    Department of Paediatrics, Derbyshire Children’s Hospital, Derby, UK

    ,
    Hazel-Ann D Borthwick

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK

    ,
    Alexandra M Yates

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK

    ,
    Emma Hubball

    Maternity Centre, University Hospital of North Staffordshire, Stoke-on-Trent, Staffordshire, UK

    ,
    Angela Rooney

    Maternity Centre, University Hospital of North Staffordshire, Stoke-on-Trent, Staffordshire, UK

    ,
    Mazeda Khanam

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK

    ,
    Neyha Aggarwal

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK

    ,
    Peter W Jones

    Department of Primary Care Sciences, Keele University, Stoke-on-Trent, Staffordshire, UK

    &
    Anthony A Fryer

    * Author for correspondence

    Institute of Science & Technology in Medicine, Keele University School of Medicine, Stoke-on-Trent, Staffordshire, UK.

    Published Online:https://doi.org/10.2217/epi.12.72

    Aim: Evidence suggests that folic acid intake affects birth weight and that these effects may be mediated via the fetal epigenome. Our previous array data indicate that methylation in human cord blood at gene-specific CpGs is associated with birth weight percentile (BWP). Our aims were to investigate associations with BWP in specific CpGs identified by the array analysis in a significantly larger cohort and investigate the effects of other relevant factors on this association. Materials & methods: Methylation status was examined in candidate CpGs in 129 cord blood samples using Pyrosequencing™. The effects of other potentially important factors; maternal smoking, folate-related metabolite levels and genetic variation in the MTHFR gene, were examined. Linear and logistic regression analyses were used to identify relationships between BWP and methylation levels in the context of other key factors. Results: Increased cord methylation at CpGs in GSTM5 and MAP2K3 was associated with a reduced risk of having a birth weight below the 50th percentile (p = 0.010; odds ratio [OR]: 0.33 and p = 0.024; OR: 0.24, respectively) while higher methylation levels in APOB were associated with an increased risk (p = 0.023; OR: 2.56). Smoking during pregnancy modified the effect of methylation on BWP. Thus, compared with nonsmokers with a GSTM5 methylation level of >25% (median BWP: 54.7%), those who had smoked during pregnancy and whose GSTM5 methylation was <25% had the lowest median BWP (12.0%; p = 0.001). Furthermore, this latter group had the highest proportion of cases with BWPs below 50% (92.9 compared with 47.8% in nonsmokers with a GSTM5 methylation level of >25%; p = 0.013; OR: 14.2). Similar results were identified for MAP2K3, while the link with APOB reflected the inverse relationship between methylation at this locus and BWP. Conclusion: Our data suggest that gene-specific methylation of cord DNA is associated with BWP and this methylation provides an additional effect on BWP to that of smoking during pregnancy.

    Papers of special note have been highlighted as: ▪ of interest ▪▪ of considerable interest

    References

    • Papadopoulou E, Stratakis N, Roumeliotaki T et al. The effect of high doses of folic acid and iron supplementation in early-to-mid pregnancy on prematurity and fetal growth retardation: the mother-child cohort study in Crete, Greece (Rhea study). Eur. J. Nutr. doi:10.1007/s00394-012-0339-z (2012) (Epub ahead of print).
    • Roberfroid D, Huybregts L, Lanou H et al. Prenatal micronutrient supplements cumulatively increase fetal growth. J. Nutr.142,548–554 (2012).
    • Taraborelli M, Ramoni V, Brucato A et al. Successful pregnancies but a higher risk of preterm births in systemic sclerosis: an Italian multicentric study. Arthritis Rheum.64,1970–1977 (2012).
    • Waterland RA. Is epigenetics an important link between early life events and adult disease? Horm. Res.71(Suppl. 1),13–16 (2009).
    • Nafee TM, Farrell WE, Carroll W, Fryer AA, Ismail KMK. Epigenetic control of fetal gene expression. Br. J. Obs. Gynaecol.115,158–168 (2008).▪▪ Provides an overview of the effects of fetal epigenetic change.
    • Tosh DN, Fu Q, Callaway CW et al. Epigenetics of programmed obesity: alteration in IUGR rat hepatic IGF1 mRNA expression and histone structure in rapid vs. delayed postnatal catch-up growth. Am. J. Physiol. Gastrointest. Liver Physiol.299,G1023–G1029 (2010).
    • Schlotz W, Phillips DI. Fetal origins of mental health: evidence and mechanisms. Brain Behav. Immun.23,905–916 (2009).
    • McCormack VA, dos Santos Silva I, De Stavola BL et al. Fetal growth and subsequent risk of breast cancer: results from long term follow up of Swedish cohort. BMJ326,248 (2003).
    • Michels KB, Harris HR, Barault L. Birthweight, maternal weight trajectories and global DNA methylation of LINE-1 repetitive elements. PLoS ONE6,e25254 (2011).▪ Emphasizes the relationship between global methylation and birth weight.
    • 10  Waterland RA, Michels KB. Epigenetic epidemiology of the developmental origins hypothesis. Annu. Rev. Nutr.27,363–388 (2007).▪▪ Outlines key experiments linking epigenetics, the intrauterine environment and later-onset disease.
    • 11  Hochberg Z, Feil R, Constancia M et al. Child health, developmental plasticity, and epigenetic programming. Endocr. Rev.32,159–224 (2011).
    • 12  Fryer AA, Nafee TM, Ismail KM, Carroll WD, Emes RD, Farrell WE. LINE-1 DNA methylation is inversely correlated with cord plasma homocysteine in man: a preliminary study. Epigenetics4,394–398 (2009).
    • 13  Fryer AA, Emes RD, Ismail KM et al. Quantitative, high-resolution epigenetic profiling of CpG loci identifies associations with cord blood plasma homocysteine and birth weight in humans. Epigenetics6,86–94 (2011).▪▪ Outlines the work that led to the studies described in this article.
    • 14  Schroeder JW, Conneely KN, Cubells JC et al. Neonatal DNA methylation patterns associate with gestational age. Epigenetics6,1498–1504 (2011).
    • 15  Suter M, Ma J, Harris A et al. Maternal tobacco use modestly alters correlated epigenome-wide placental DNA methylation and gene expression. Epigenetics6,1284–1294 (2011).
    • 16  Bakker R, Timmermans S, Steegers EA, Hofman A, Jaddoe VW. Folic acid supplements modify the adverse effects of maternal smoking on fetal growth and neonatal complications. J. Nutr.141,2172–2179 (2011).▪ Illustrates the importance of smoking during pregnancy on the relationship between methyl group supply and fetal growth.
    • 17  Furness DL, Yasin N, Dekker GA, Thompson SD, Roberts CT. Maternal red blood cell folate concentration at 10–12 weeks gestation and pregnancy outcome. J. Matern. Fetal Neonatal Med.25,1423–1427 (2012).
    • 18  Frelut ML, Nicolas JP, Guilland JC, de Courcy GP. Methylenetetrahydrofolate reductase 677 C->T polymorphism: a link between birth weight and insulin resistance in obese adolescents. Int. J. Pediatr. Obes.6,e312–317 (2011).
    • 19  Relton CL, Pearce MS, Burn J, Parker L. An investigation of folate-related genetic factors in the determination of birthweight. Paediatr. Perinat. Epidemiol.19,360–367 (2005).▪ Highlights the key role of genetic variation in key members of the folate pathway as determinants of birth weight.
    • 20  Boeke CE, Baccarelli A, Kleinman KP et al. Gestational intake of methyl donors and global LINE-1 DNA methylation in maternal and cord blood: prospective results from a folate-replete population. Epigenetics7,253–260 (2012).
    • 21  Mill J, Yazdanpanah S, Gukel E, Ziegler S, Kaminsky Z, Petronis A. Whole genome amplification of sodium bisulfite-treated DNA allows the accurate estimate of methylated cytosine density in limited DNA resources. Biotechniques41,603–607 (2006).
    • 22  Hoyo C, Fortner K, Murtha AP et al. Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight. Cancer Causes Control23,635–645 (2012).
    • 23  McKay JA, Groom A, Potter C et al. Genetic and non-genetic influences during pregnancy on infant global and site specific DNA methylation: role for folate gene variants and vitamin B(12). PLoS ONE7,e33290 (2012).
    • 24  Flom JD, Ferris JS, Liao Y et al. Prenatal smoke exposure and genomic DNA methylation in a multiethnic birth cohort. Cancer Epidemiol. Biomarkers Prev.20,2518–2523 (2011).
    • 25  Ba Y, Yu H, Liu F et al. Relationship of folate, vitamin B12 and methylation of insulin-like growth factor-II in maternal and cord blood. Eur. J. Clin. Nutr.65,480–485 (2011).
    • 26  Yila TA, Sasaki S, Miyashita C et al. Effects of maternal 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and tobacco smoking on infant birth weight in a Japanese population. J. Epidemiol.22,91–102 (2012).▪▪ Brings together the associations between genetic variation and maternal smoking, and birth weight.
    • 27  Wilhelm-Benartzi CS, Houseman EA, Maccani MA et al. In utero exposures, infant growth, and DNA methylation of repetitive elements and developmentally related genes in human placenta. Environ. Health Perspect.120,296–302 (2012).
    • 28  Kordas K, Ettinger AS, Lamadrid-Figueroa H et al. Methylenetetrahydrofolatereductase (MTHFR) C677T, A1298C and G1793A genotypes, and the relationship between maternal folate intake, tibia lead and infant size at birth. Br. J. Nutr.102,907–914 (2009).
    • 29  Fraser HB, Lam L, Neumann S, Kobor MS. Population-specificity of human DNA methylation. Genome Biol.13,R8 (2012).
    • 30  Boks MP, Derks EM, Weisenberger DJ et al. The relationship of DNA methylation with age, gender and genotype in twins and healthy controls. PLoS ONE4,e6767 (2009).
    • 31  Schilling E, Chartouni C, Rehli M. Allele-specific DNA methylation in mouse strains is mainly determined by cis-acting sequences. Genome Res.19,2028–2035 (2009).
    • 32  Sasaki H, Hamada T, Ueda T, Seki R, Higashinakagawa T, Sakaki Y. Inherited type of allelic methylation variations in a mouse chromosome region where an integrated transgene shows methylation imprinting. Development111,573–581 (1991).
    • 101  Gestation Network. www.gestation.net
    • 102  AmplifX 1.6.1 by Nicolas Jullien; CNRS, Aix-Marseille Université. http://crn2m.univ-mrs.fr/recherche/equipe-t-brue/jullien-nicolas/programmation/amplifx