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Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy

Metabolic profiles of amniotic fluid and maternal blood are sources of valuable information about fetus development and can be potentially useful in diagnosis of pregnancy disorders. In this study, we applied (1)H NMR-based metabolic profiling to track metabolic changes occurring in amniotic fluid (...

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Autores principales: Orczyk-Pawilowicz, Magdalena, Jawien, Ewa, Deja, Stanislaw, Hirnle, Lidia, Zabek, Adam, Mlynarz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829258/
https://www.ncbi.nlm.nih.gov/pubmed/27070784
http://dx.doi.org/10.1371/journal.pone.0152740
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author Orczyk-Pawilowicz, Magdalena
Jawien, Ewa
Deja, Stanislaw
Hirnle, Lidia
Zabek, Adam
Mlynarz, Piotr
author_facet Orczyk-Pawilowicz, Magdalena
Jawien, Ewa
Deja, Stanislaw
Hirnle, Lidia
Zabek, Adam
Mlynarz, Piotr
author_sort Orczyk-Pawilowicz, Magdalena
collection PubMed
description Metabolic profiles of amniotic fluid and maternal blood are sources of valuable information about fetus development and can be potentially useful in diagnosis of pregnancy disorders. In this study, we applied (1)H NMR-based metabolic profiling to track metabolic changes occurring in amniotic fluid (AF) and plasma (PL) of healthy mothers over the course of pregnancy. AF and PL samples were collected in the 2(nd) (T2) and 3(rd) (T3) trimester, prolonged pregnancy (PP) until time of delivery (TD). A multivariate data analysis of both biofluids reviled a metabolic switch-like transition between 2(nd) and 3(rd) trimester, which was followed by metabolic stabilization throughout the rest of pregnancy probably reflecting the stabilization of fetal maturation and development. The differences were further tested using univariate statistics at α = 0.001. In plasma the progression from T2 to T3 was related to increasing levels of glycerol, choline and ketone bodies (3-hydroxybutyrate and acetoacetate) while pyruvate concentration was significantly decreased. In amniotic fluid, T2 to T3 transition was associated with decreasing levels of glucose, carnitine, amino acids (valine, leucine, isoleucine, alanine, methionine, tyrosine, and phenylalanine) and increasing levels of creatinine, succinate, pyruvate, choline, N,N-dimethylglycine and urocanate. Lactate to pyruvate ratio was decreased in AF and conversely increased in PL. The results of our study, show that metabolomics profiling can be used to better understand physiological changes of the complex interdependencies of the mother, the placenta and the fetus during pregnancy. In the future, these results might be a useful reference point for analysis of complicated pregnancies.
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spelling pubmed-48292582016-04-22 Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy Orczyk-Pawilowicz, Magdalena Jawien, Ewa Deja, Stanislaw Hirnle, Lidia Zabek, Adam Mlynarz, Piotr PLoS One Research Article Metabolic profiles of amniotic fluid and maternal blood are sources of valuable information about fetus development and can be potentially useful in diagnosis of pregnancy disorders. In this study, we applied (1)H NMR-based metabolic profiling to track metabolic changes occurring in amniotic fluid (AF) and plasma (PL) of healthy mothers over the course of pregnancy. AF and PL samples were collected in the 2(nd) (T2) and 3(rd) (T3) trimester, prolonged pregnancy (PP) until time of delivery (TD). A multivariate data analysis of both biofluids reviled a metabolic switch-like transition between 2(nd) and 3(rd) trimester, which was followed by metabolic stabilization throughout the rest of pregnancy probably reflecting the stabilization of fetal maturation and development. The differences were further tested using univariate statistics at α = 0.001. In plasma the progression from T2 to T3 was related to increasing levels of glycerol, choline and ketone bodies (3-hydroxybutyrate and acetoacetate) while pyruvate concentration was significantly decreased. In amniotic fluid, T2 to T3 transition was associated with decreasing levels of glucose, carnitine, amino acids (valine, leucine, isoleucine, alanine, methionine, tyrosine, and phenylalanine) and increasing levels of creatinine, succinate, pyruvate, choline, N,N-dimethylglycine and urocanate. Lactate to pyruvate ratio was decreased in AF and conversely increased in PL. The results of our study, show that metabolomics profiling can be used to better understand physiological changes of the complex interdependencies of the mother, the placenta and the fetus during pregnancy. In the future, these results might be a useful reference point for analysis of complicated pregnancies. Public Library of Science 2016-04-12 /pmc/articles/PMC4829258/ /pubmed/27070784 http://dx.doi.org/10.1371/journal.pone.0152740 Text en © 2016 Orczyk-Pawilowicz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Orczyk-Pawilowicz, Magdalena
Jawien, Ewa
Deja, Stanislaw
Hirnle, Lidia
Zabek, Adam
Mlynarz, Piotr
Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy
title Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy
title_full Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy
title_fullStr Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy
title_full_unstemmed Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy
title_short Metabolomics of Human Amniotic Fluid and Maternal Plasma during Normal Pregnancy
title_sort metabolomics of human amniotic fluid and maternal plasma during normal pregnancy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829258/
https://www.ncbi.nlm.nih.gov/pubmed/27070784
http://dx.doi.org/10.1371/journal.pone.0152740
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