生物体液代谢分析有助于改善孕期保健吗

G. Graça, Sílvia O. Diaz, J. Pinto, António S. Barros, I. Duarte, B. Goodfellow, E. Galhano, Cristina Pita, Maria do Céu Almeida, I. Carreira, Ana M. Gil
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引用次数: 13

摘要

本文介绍了一项妊娠中期生物体液(羊水、产妇尿液和血浆)的代谢组学研究,试图将生物体液代谢变化与疑似/诊断的胎儿畸形(FM)和染色体疾病以及后期发生的妊娠糖尿病(GDM)、早产(PTD)和胎膜早破(PROM)联系起来。这三种生物流体所提供的全球生物化学图谱应该能够定义潜在的疾病特征,并揭示潜在的代谢物标记物,用于预测性产前诊断的临床应用。结果表明,相对较强的代谢紊乱伴随FM,反映在所有三种生物体液中,从而表明胎儿和母亲的代谢都参与其中。对于GDM,羊水和产妇尿液似乎是检测早期代谢变化的潜在良好介质,PTD受试者在相同的生物体液中显示出较小的代谢物变化,正在进行血浆成分的研究。有趣的是,染色体疾病对母体尿液有显著影响,而在早膜PROM患者中没有观察到统计学上相关的早期变化。有趣的是,在FM和染色体疾病的情况下,母体生物液对疾病类型有一定的敏感性,例如,分别对中枢神经系统畸形和21三体病敏感。这些结果表明,生物流体代谢组学的有用性,以探索有关产前疾病的整体代谢紊乱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can Biofluids Metabolic Profiling Help to Improve Healthcare during Pregnancy
This paper describes a metabonomics study of 2nd trimester biofluids (amniotic fluid, maternal urine, and blood plasma), in an attempt to correlate biofluid metabolic changes with suspected/diagnosed fetal malformations (FM) and chromosomal disorders as well as with later occurring gestational diabetes mellitus (GDM), preterm delivery (PTD), and premature rupture of membranes (PROM). The global biochemical picture given by the threesome of biofluids should enable the definition of potential disease signatures and unveil potential metabolite markers for clinical use in predictive prenatal diagnostics. Results show that relatively strong metabolic disturbances accompany FM, reflected in all three biofluids and thus suggesting the involvement of both fetal and maternal metabolisms. Regarding GDM, amniotic fluid and maternal urine seem potential good media to detect early metabolic changes, and PTD subjects show small metabolite changes in the same biofluids, undergoing work being focused on plasma composition. Chromosomal disorders show an interestingly marked effect on maternal urine, whereas no statistically relevant early changes have been observed for PROM subjects. Interestingly, in the case of FM and chromosomal disorders, maternal biofluids show some sensitivity to disorder type, for example, for central nervous system malformations and trisomy 21, respectively. These results show the usefulness of biofluid metabonomics to probe overall metabolic disturbances in relation to prenatal disorders.
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