Impact of Prenatal Disorders on the Metabolic Profile of Second Trimester Amniotic Fluid: A Nuclear Magnetic Resonance Metabonomic Study

被引:86
作者
Graca, Goncalo [1 ]
Duarte, Iola F. [1 ]
Barros, Antonio S. [2 ]
Goodfellow, Brian J. [1 ]
Diaz, Silvia O. [1 ]
Pinto, Joana [1 ]
Carreira, Isabel M. [3 ,4 ]
Galhano, Eulalia [5 ]
Pita, Cristina [5 ]
Gil, Ana M. [1 ]
机构
[1] Univ Aveiro, CICECO, Dept Chem, P-3810193 Aveiro, Portugal
[2] Univ Aveiro, QOPNA Res Unit, Dept Chem, P-3810193 Aveiro, Portugal
[3] Univ Coimbra, Fac Med, Cytogenet Lab, P-3000354 Coimbra, Portugal
[4] Univ Coimbra, Fac Med, Ctr Neurosci & Cellular Biol, P-3000354 Coimbra, Portugal
[5] Ctr Hosp Coimbra, P-3000 Coimbra, Portugal
关键词
Amniotic fluid; prenatal disorders; fetal malformations; gestational diabetes; preterm; NMR spectroscopy; metabonomics; FETAL LUNG MATURITY; NMR-SPECTROSCOPY; OXIDATIVE STRESS; MASS-SPECTROMETRY; PREGNANCIES; FETUSES; ACIDS;
D O I
10.1021/pr100815q
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes a metabonomic study of prenatal disorders using nuclear magnetic resonance (NMR) spectroscopy of amniotic fluid (AF) collected in the second trimester of pregnancy, to search for metabolite markers of fetal malformations, prediagnostic gestational diabetes (GD), preterm delivery (PTD), early rupture of membranes (PROM), and chromossomopathies. Fetal malformations were found to have the highest impact on AF metabolite composition, enabling statistical validation to be achieved by several multivariate analytical tools. Results confirmed previous indications that malformed fetuses seem to suffer altered energy metabolism and kidney underdevelopment. Newly found changes (namely in a-oxoisovalerate, ascorbate, creatinine, isoleucine, serine, threonine) suggest possible additional effects on protein and nucleotide sugar biosynthesis. Prediagnostic GD subjects showed an average increase in glucose and small decreases in several amino acids along with acetate, formate, creatinine, and glycerophosphocholine. Small metabolite changes were also observed in the AF of subjects eventually undergoing PTD and PROM, whereas no relevant changes were found for chromossomopathies (for which a low number of samples was considered). The potential value of these results for biochemical insight and prediction of prenatal disorders is discussed, as well as their limitations regarding number of samples and overlap of different disorders.
引用
收藏
页码:6016 / 6024
页数:9
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