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Relationship between placental expression of the imprinted PHLDA2 gene, intrauterine skeletal growth and childhood bone mass.

机译:印记的PHLDA2基因的胎盘表达与子宫内骨骼生长和儿童骨骼质量之间的关系。

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摘要

Alterations in expression of the imprinted gene PHLDA2 are linked to low birth weight in both humans and the mouse. However birth weight is a summary measure of fetal growth and provides little information on the growth rate of the fetus in early and late pregnancy. To examine the relation of PHLDA2 expression with rates of fetal growth and explore associations with the infant's body composition in early childhood, we measured PHLDA2 mRNA levels in the term placenta of 102 infants whose mothers were participating in the Southampton Women's Survey (SWS). Higher PHLDA2 expression was associated with a lower fetal femur growth velocity between 19 and 34 weeks gestation. In addition, higher placental PHLDA2 gene expression was associated with a lower child's bone mineral content at four years of age, measured using dual-energy X-ray absorptiometry. The results suggest that placental PHLDA2 may provide a biomarker for suboptimal skeletal growth in pregnancies uncomplicated by overt fetal growth restriction.
机译:印迹基因PHLDA2表达的改变与人类和小鼠的低出生体重有关。然而,出生体重是胎儿生长的概括指标,几乎没有提供有关妊娠早期和晚期胎儿生长速率的信息。为了检查PHLDA2表达与胎儿生长速率之间的关系并探讨与婴儿早期身体成分的关系,我们在母亲参加南安普敦妇女调查(SWS)的102例婴儿的胎盘中测量了PHLDA2 mRNA的水平。在妊娠19至34周之间,较高的PHLDA2表达与较低的胎儿股骨生长速度有关。此外,使用双能X射线吸收法测定的结果表明,胎盘PHLDA2基因的较高表达与4岁儿童的骨矿物质含量较低相关。结果表明,胎盘PHLDA2可能为未受到明显胎儿生长限制的复杂妊娠提供次佳骨骼生长的生物标志物。

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