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Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight.

Publication ,  Journal Article
Hoyo, C; Fortner, K; Murtha, AP; Schildkraut, JM; Soubry, A; Demark-Wahnefried, W; Jirtle, RL; Kurtzberg, J; Forman, MR; Overcash, F; Huang, Z ...
Published in: Cancer Causes Control
April 2012

PURPOSE: Altered methylation at Insulin-like Growth Factor 2 (IGF2) regulatory regions has previously been associated with obesity, and several malignancies including colon, esophageal, and prostate adenocarcinomas, presumably via changes in expression and/or loss of imprinting, but the functional significance of these DNA methylation marks have not been demonstrated in humans. We examined associations among DNA methylation at IGF2 differentially methylated regions (DMRs), circulating IGF2 protein concentrations in umbilical cord blood (UCB) and birth weight in newborns. METHODS: Questionnaire data were obtained from 300 pregnant women recruited between 2005 and 2009. UCB DNA methylation was measured by bisulfite pyrosequencing. UCB plasma concentrations of soluble IGF2 were measured by ELISA assays. Generalized linear regression models were used to examine the relationship between DMR methylation and IGF2 levels. RESULTS: Lower IGF2 DMR methylation was associated with elevated plasma IGF2 protein concentrations (β = -9.87, p < 0.01); an association that was stronger in infants born to obese women (pre-pregnancy BMI > 30 kg/m(2), β = -20.21, p < 0.0001). Elevated IGF2 concentrations were associated with higher birth weight (p < 0.0001) after adjusting for maternal race/ethnicity, pre-pregnancy BMI, cigarette smoking, gestational diabetes, and infant sex. These patterns of association were not apparent at the H19 DMR. CONCLUSION: Our data suggest that variation in IGF2 DMR methylation is an important mechanism by which circulating IGF2 concentrations, a putative risk factor for obesity and cancers of the colon, esophagus, and prostate, are modulated; associations that may depend on pre-pregnancy obesity.

Duke Scholars

Published In

Cancer Causes Control

DOI

EISSN

1573-7225

Publication Date

April 2012

Volume

23

Issue

4

Start / End Page

635 / 645

Location

Netherlands

Related Subject Headings

  • Male
  • Insulin-Like Growth Factor II
  • Infant, Newborn
  • Humans
  • Genomic Imprinting
  • Fetal Blood
  • Female
  • Epidemiology
  • Enzyme-Linked Immunosorbent Assay
  • DNA Methylation
 

Citation

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MLA
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Hoyo, C., Fortner, K., Murtha, A. P., Schildkraut, J. M., Soubry, A., Demark-Wahnefried, W., … Murphy, S. K. (2012). Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight. Cancer Causes Control, 23(4), 635–645. https://doi.org/10.1007/s10552-012-9932-y
Hoyo, Cathrine, Kimberly Fortner, Amy P. Murtha, Joellen M. Schildkraut, Adelheid Soubry, Wendy Demark-Wahnefried, Randy L. Jirtle, et al. “Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight.Cancer Causes Control 23, no. 4 (April 2012): 635–45. https://doi.org/10.1007/s10552-012-9932-y.
Hoyo C, Fortner K, Murtha AP, Schildkraut JM, Soubry A, Demark-Wahnefried W, et al. Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight. Cancer Causes Control. 2012 Apr;23(4):635–45.
Hoyo, Cathrine, et al. “Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight.Cancer Causes Control, vol. 23, no. 4, Apr. 2012, pp. 635–45. Pubmed, doi:10.1007/s10552-012-9932-y.
Hoyo C, Fortner K, Murtha AP, Schildkraut JM, Soubry A, Demark-Wahnefried W, Jirtle RL, Kurtzberg J, Forman MR, Overcash F, Huang Z, Murphy SK. Association of cord blood methylation fractions at imprinted insulin-like growth factor 2 (IGF2), plasma IGF2, and birth weight. Cancer Causes Control. 2012 Apr;23(4):635–645.
Journal cover image

Published In

Cancer Causes Control

DOI

EISSN

1573-7225

Publication Date

April 2012

Volume

23

Issue

4

Start / End Page

635 / 645

Location

Netherlands

Related Subject Headings

  • Male
  • Insulin-Like Growth Factor II
  • Infant, Newborn
  • Humans
  • Genomic Imprinting
  • Fetal Blood
  • Female
  • Epidemiology
  • Enzyme-Linked Immunosorbent Assay
  • DNA Methylation