Metabolic characterization of amniotic fluids of fetuses with enlarged nuchal translucency.


Journal

Journal of perinatal medicine
ISSN: 1619-3997
Titre abrégé: J Perinat Med
Pays: Germany
ID NLM: 0361031

Informations de publication

Date de publication:
24 Apr 2019
Historique:
received: 18 09 2018
accepted: 08 01 2019
pubmed: 14 2 2019
medline: 5 9 2019
entrez: 14 2 2019
Statut: ppublish

Résumé

Background In prenatal diagnosis, a thickened nuchal translucency (NT) is one of the most sensitive and specific markers for several defects but it may also be found in 5% of healthy fetuses. The pathophysiological causes that lead to an increase in NT are not yet fully understood. Metabolomics represents a new promising approach, useful for studying different metabolites in biological organisms in response to environmental stressors. The aim of our study was to investigate the metabolomic profile of the amniotic fluid samples (AFS) of euploid fetuses with enlarged nuchal translucency (ENT) compared to a control group (C group). Methods This study was carried out on a group of women who underwent second-trimester amniocentesis for advanced maternal age (C group) or for NT ≥95th percentile (ENT group) found during first-trimester aneuploidy screening. AFS were analyzed with proton nuclear magnetic resonance (1H-NMR) and high-performance liquid chromatography (HPLC), and subsequent multivariate and univariate statistical analyses were conducted, followed by pathway analysis. Results In total, 67 AFS from the C group and 23 from the ENT group were analyzed. Partial least square discriminate analysis was carried out (R2X=0.784, R2Y=0.658, Q2=0.622, P<0.0001). A different metabolic profile was observed in the ENT group compared with the C group, suggesting an energetic shift to a glycolytic phenotype in an oxidative environment in the ENT group compared to the C group. Conclusion Metabolomic studies enable the identification of metabolic alterations occurring in fetuses with ENT. These findings may provide a new basis for better understanding the pathophysiological mechanisms in this prenatal phenomenon.

Identifiants

pubmed: 30759069
doi: 10.1515/jpm-2018-0314
pii: /j/jpme.ahead-of-print/jpm-2018-0314/jpm-2018-0314.xml
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

311-318

Auteurs

Ambra Iuculano (A)

Department of Prenatal and Preimplantation Genetic Diagnosis and Fetal Therapy, Ospedale Microcitemico, Cagliari, Italy.

Federica Murgia (F)

Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, Cagliari, Italy.

Cristina Peddes (C)

Department of Prenatal and Preimplantation Genetic Diagnosis and Fetal Therapy, Ospedale Microcitemico, Cagliari, Italy.

Maria Laura Santoru (ML)

Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, Cagliari, Italy.

Laura Tronci (L)

Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, Cagliari, Italy.

Monica Deiana (M)

Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, Cagliari, Italy.

Antonella Balsamo (A)

Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, Cagliari, Italy.

Anna Euser (A)

Department of Maternal-Fetal Medicine, University of Colorado, Anschutz Medical Campus, Denver, CO, USA.

Luigi Atzori (L)

Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, Cagliari, Italy.

Giovanni Monni (G)

Department of Prenatal and Preimplantation Genetic Diagnosis and Fetal Therapy, Ospedale Microcitemico, Via E. Jenner n/n, 09121 Cagliari, Italy.

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Classifications MeSH