Metabolic Infrastructure of Pregnant Women With Trisomy 21 Fetuses; Metabolomic Analysis


NEMUTLU E., ÖRGÜL G., REÇBER T., AYDIN E., ÖZKAN E., TURĞAL M., ...More

ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE, vol.223, no.5, pp.297-303, 2019 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 223 Issue: 5
  • Publication Date: 2019
  • Doi Number: 10.1055/a-0877-7869
  • Journal Name: ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.297-303
  • Keywords: Down syndrome, Gas Chromatography-Mass Spectrometry, Liquid Chromatography-Mass Spectrometry, Metabolomics, DNA, ACID

Abstract

We aimed to configure impaired/altered metabolomic profiles of pregnant women carrying Down syndrome (DS) fetuses. The study involved 21 and 32 pregnant women with DS and euploid fetuses, respectively, as determined by prenatal screening and diagnosis as part of an antenatal care program. Metabolomic analyses were carried out using gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-quadrupole time- of-flight mass spectrometry (LC-qTOF-MS) methods. A total of 95 metabolites were identified. GC-MS analysis indicated that levels of 2-hydroxybutyric acid, benzoic acid, nonanoic acid, 3-hydroxybutyric acid, and 2-ketoisocaproic acid were increased in the DS group, where beta-alanine, threonic acid, oxalic acid, alpha-tocopherol, uracil, 2-piperidone, and creatinine were decreased. However, LC-qTOF-MS analysis showed that lipid-related metabolites were decreased in women carrying DS fetuses, whereas creatine, N4-phosphoagmatine, citrate, 2,5-dioxopentanoate, 2-furoate, pyruvate, and fructose levels were increased. Pathway analysis was also performed using metabolites whose levels were significantly altered (p < 0.05) between the groups, and the findings indicated that the biosynthesis pathways of aminoacyl-tRNA and "valine-leucine-isoleucine", and metabolism pathways of "glycine-serine-threonine", nitrogen, "alanine-aspartate-glutamate", propanoate, glycerophospholipid, cysteine, methionine, and phenylalanine were significantly altered. Our findings indicate a special type of metabolic status/syndrome in pregnant women with Down syndrome fetuses. It could be speculated that altered metabolic status might influence both gametogenesis and embryogenesis. Down syndrome is a complex genetic disorder that is important to detect prenatally, but may also be prevented by taking necessary precautions prior to pregnancy.