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与胎龄小相关的生理学的甘油磷脂和解毒途径:SCOPE 队列中的发现代谢组学分析。

Glycerophospholipid and detoxification pathways associated with small for gestation age pathophysiology: discovery metabolomics analysis in the SCOPE cohort.

机构信息

INFANT Research Centre, Cork University Hospital, Wilton, Cork, Ireland.

Department of Obstetrics and Gynecology, University College Cork, Cork, Ireland.

出版信息

Metabolomics. 2021 Jan 5;17(1):5. doi: 10.1007/s11306-020-01740-9.

Abstract

INTRODUCTION

Small for gestational age (SGA) may be associated with neonatal morbidity and mortality. Our understanding of the molecular pathways implicated is poor.

OBJECTIVES

Our aim was to determine the metabolic pathways involved in the pathophysiology of SGA and examine their variation between maternal biofluid samples.

METHODS

Plasma (Cork) and urine (Cork, Auckland) samples were collected at 20 weeks' gestation from nulliparous low-risk pregnant women participating in the SCOPE study. Women who delivered an SGA infant (birthweight < 10th percentile) were matched to controls (uncomplicated pregnancies). Metabolomics (urine) and lipidomics (plasma) analyses were performed using ultra performance liquid chromatography-mass spectrometry. Features were ranked based on FDR adjusted p-values from empirical Bayes analysis, and significant features putatively identified.

RESULTS

Lipidomics plasma analysis revealed that 22 out of the 33 significantly altered lipids annotated were glycerophospholipids; all were detected in higher levels in SGA. Metabolomic analysis identified reduced expression of metabolites associated with detoxification (D-Glucuronic acid, Estriol-16-glucuronide), nutrient absorption and transport (Sulfolithocholic acid) pathways.

CONCLUSIONS

This study suggests higher levels of glycerophospholipids, and lower levels of specific urine metabolites are implicated in the pathophysiology of SGA. Further research is needed to confirm these findings in independent samples.

摘要

简介

胎儿生长受限(SGA)可能与新生儿发病率和死亡率有关。我们对其涉及的分子途径知之甚少。

目的

本研究旨在确定与 SGA 病理生理学相关的代谢途径,并检查它们在母体生物流体样本之间的变化。

方法

在 SCOPE 研究中,从参与研究的初产妇低风险孕妇中收集 20 周妊娠的血浆(科克)和尿液(科克、奥克兰)样本。将分娩 SGA 婴儿(出生体重<第 10 百分位数)的女性与对照组(无并发症妊娠)相匹配。使用超高效液相色谱-质谱联用进行代谢组学(尿液)和脂质组学(血浆)分析。基于经验贝叶斯分析的 FDR 调整 p 值对特征进行排名,并推测出显著特征。

结果

脂质组学血浆分析显示,33 个显著改变的脂质中有 22 个被注释为甘油磷脂;所有 SGA 中均检测到更高水平的甘油磷脂。代谢组学分析确定了与解毒(D-葡萄糖醛酸、雌三醇-16-葡萄糖醛酸)、营养吸收和转运(磺基胆酸)途径相关的代谢物表达降低。

结论

本研究表明,SGA 病理生理学中涉及更高水平的甘油磷脂和特定尿液代谢物水平降低。需要在独立样本中进一步研究以确认这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41b8/7782411/a9c4bd3325f1/11306_2020_1740_Fig1_HTML.jpg

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