Birthweight, Maternal Weight Trajectories and Global DNA Methylation of LINE-1 Repetitive Elements
2011

Birthweight and DNA Methylation in Newborns

Sample size: 319 publication 10 minutes Evidence: moderate

Author Information

Author(s): Michels Karin B., Harris Holly R., Barault Ludovic

Primary Institution: Brigham and Women's Hospital, Harvard Medical School

Hypothesis

How do fetal and maternal weight trajectories affect LINE-1 methylation in newborns?

Conclusion

The study found significant differences in LINE-1 methylation levels in cord blood among newborns with low and high birthweight as well as among prematurely born infants.

Supporting Evidence

  • Newborns with low or high birthweight had significantly lower LINE-1 methylation levels in their cord blood compared to normal weight infants.
  • Infants born prematurely also had lower LINE-1 methylation levels in cord blood compared to term infants.
  • The magnitude of the difference in methylation levels was small but statistically significant.

Takeaway

Babies who are born too small or too big have different levels of a special chemical in their blood that can affect their health later on.

Methodology

The study analyzed cord blood and placenta samples from 319 mother-child dyads to assess the relationship between birthweight and LINE-1 methylation.

Limitations

The study did not find important associations between maternal weight trajectories and global methylation in cord blood or placental tissue.

Participant Demographics

The study included 319 mother-child dyads with a median maternal age of 32 years and various ethnic backgrounds.

Statistical Information

P-Value

p=0.004 for preterm birth and p=0.007 for low birthweight

Confidence Interval

95% CI for difference in methylation ranged from -1.42 to -0.23 for low birthweight

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0025254

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