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The newborn metabolome: associations with gestational diabetes, sex, gestation, birth mode, and birth weight
Pediatric Research ( IF 3.6 ) Pub Date : 2021-09-15 , DOI: 10.1038/s41390-021-01672-7
Toby Mansell 1, 2 , Amanda Vlahos 1 , Fiona Collier 1, 3, 4 , Anne-Louise Ponsonby 1, 2, 5 , Peter Vuillermin 1, 3, 4 , Susan Ellul 1 , Mimi L K Tang 1, 2, 6 , David Burgner 1, 2, 7 , Richard Saffery 1, 2 ,
Affiliation  

Background

Pathways towards many adult-onset conditions begin early in life, even in utero. Maternal health in pregnancy influences this process, but little is known how it affects neonatal metabolism. We investigated associations between pregnancy and birth factors and cord blood metabolomic profile in a large, population-derived cohort.

Methods

Metabolites were measured using nuclear magnetic resonance in maternal (28 weeks gestation) and cord serum from 912 mother–child pairs in the Barwon Infant Study pre-birth cohort. Associations between maternal (metabolites, age, BMI, smoking), pregnancy (pre-eclampsia, gestational diabetes (GDM)), and birth characteristics (delivery mode, gestational age, weight, infant sex) with 72 cord blood metabolites were examined by linear regression.

Results

Delivery mode, sex, gestational age, and birth weight were associated with specific metabolite levels in cord blood, including amino acids, fatty acids, and cholesterols. GDM was associated with higher cord blood levels of acetoacetate and 3-hydroxybutyrate.

Conclusions

Neonatal factors, particularly delivery mode, were associated with many cord blood metabolite differences, including those implicated in later risk of cardiometabolic disease. Associations between GDM and higher offspring ketone levels at birth are consistent with maternal ketosis in diabetic pregnancies. Further work is needed to determine whether these neonatal metabolome differences associate with later health outcomes.

Impact

  • Variations in blood metabolomic profile have been linked to health status in adults and children, but corresponding data in neonates are scarce.

  • We report evidence that pregnancy complications, mode of delivery, and offspring characteristics, including sex, are independently associated with a range of circulating metabolites at birth, including ketone bodies, amino acids, cholesterols, and inflammatory markers.

  • Independent of birth weight, exposure to gestational diabetes is associated with higher cord blood ketone bodies and citrate.

  • These findings suggest that pregnancy complications, mode of delivery, gestational age, and measures of growth influence metabolic pathways prior to birth, potentially impacting later health and development.



中文翻译:

新生儿代谢组:与妊娠糖尿病、性别、妊娠、分娩方式和出生体重的关联

背景

许多成人发病的途径在生命早期就开始了,甚至在子宫内就开始了。怀孕期间的母亲健康会影响这一过程,但鲜为人知的是它如何影响新生儿的新陈代谢。我们在一个大型人群衍生队列中调查了妊娠和出生因素与脐带血代谢组学特征之间的关联。

方法

在 Barwon 婴儿研究出生前队列的 912 对母子中,使用核磁共振对母体(妊娠 28 周)和脐带血清中的代谢物进行了测量。产妇(代谢物、年龄、BMI、吸烟)、妊娠(先兆子痫、妊娠糖尿病 (GDM))和出生特征(分娩方式、胎龄、体重、婴儿性别)与 72 种脐带血代谢物之间的关联通过线性检测回归。

结果

分娩方式、性别、胎龄和出生体重与脐带血中的特定代谢物水平相关,包括氨基酸、脂肪酸和胆固醇。GDM 与较高的脐带血乙酰乙酸和 3-羟基丁酸水平有关。

结论

新生儿因素,尤其是分娩方式,与许多脐带血代谢物差异有关,包括那些与后来的心脏代谢疾病风险有关的差异。GDM 与出生时较高的后代酮水平之间的关联与糖尿病妊娠中的母体酮症一致。需要进一步的工作来确定这些新生儿代谢组差异是否与以后的健康结果相关。

影响

  • 血液代谢组学特征的变化与成人和儿童的健康状况有关,但新生儿的相应数据很少。

  • 我们报告的证据表明,妊娠并发症、分娩方式和后代特征(包括性别)与出生时的一系列循环代谢物独立相关,包括酮体、氨基酸、胆固醇和炎症标志物。

  • 独立于出生体重,暴露于妊娠糖尿病与较高的脐带血酮体和柠檬酸盐有关。

  • 这些发现表明,妊娠并发症、分娩方式、胎龄和生长指标会影响出生前的代谢途径,并可能影响以后的健康和发育。

更新日期:2021-09-16
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