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IGF-II expression and methylation in small for gestational age infants
Journal of Pediatric Endocrinology & Metabolism : JPEM
|December 16, 2014
Summary
Insulin-like growth factor II (IGF-II) levels are linked to birth weight. H19 differentially methylated regions (DMR) methylation may influence IGF-II expression in newborns, impacting later health outcomes.
Area of Science:
- Endocrinology
- Genetics
- Neonatal Health
Background:
- Low birth weight is a risk factor for adult diseases.
- Investigated Insulin-like Growth Factor II (IGF-II) expression and differentially methylated regions (DMR) in small for gestational age (SGA) infants.
Purpose of the Study:
- To examine the relationship between birth weight and IGF-II expression and methylation patterns.
- To understand the role of IGF-II and H19 DMR in SGA infants.
Main Methods:
- Measured plasma levels of IGF-II, IGF2R, IGF-I, and IGFBP3 in 150 newborns.
- Quantified IGF2 mRNA and H19 mRNA using quantitative PCR.
- Assessed H19 and IGF2 DMR methylation status via methylation-specific PCR (MSP).
Main Results:
- Lower plasma IGF-II levels were observed in term SGA and large for gestational age (LGA) infants compared to appropriate for gestational age (AGA) infants.
- IGF2 mRNA expression was higher in term SGA than preterm SGA infants.
- H19 DMR methylation levels were elevated in both term SGA and LGA infants versus term AGA infants.
Conclusions:
- IGF-II is associated with birth weight and shows high postnatal expression, suggesting continued importance.
- H19 DMR methylation may play a role in regulating IGF-II expression postnatally.
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