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Metabolite Profile of Cervicovaginal Fluids from Early Pregnancy Is Not Predictive of Spontaneous Preterm Birth.
Thomas, Melinda M; Sulek, Karolina; McKenzie, Elizabeth J; Jones, Beatrix; Han, Ting-Li; Villas-Boas, Silas G; Kenny, Louise C; McCowan, Lesley M E; Baker, Philip N.
Afiliación
  • Thomas MM; Liggins Institute, University of Auckland, 85 Park Road, Auckland 1023, New Zealand. m.thomas@auckland.ac.nz.
  • Sulek K; Liggins Institute, University of Auckland, 85 Park Road, Auckland 1023, New Zealand. k.sulek@auckland.ac.nz.
  • McKenzie EJ; Liggins Institute, University of Auckland, 85 Park Road, Auckland 1023, New Zealand. liz.mckenzie@auckland.ac.nz.
  • Jones B; Institute of Natural and Mathematical Sciences, Massey University, Albany Campus, Auckland 0632, New Zealand. m.b.jones@massey.ac.nz.
  • Han TL; Liggins Institute, University of Auckland, 85 Park Road, Auckland 1023, New Zealand. t.han@auckland.ac.nz.
  • Villas-Boas SG; School of Biological Sciences, University of Auckland, 3a Symonds Street, Auckland 1010, New Zealand. s.villas-boas@auckland.ac.nz.
  • Kenny LC; The Irish Centre for Fetal and Neonatal Translational Research, University College Cork, Wilton 06897, Cork, Ireland. l.kenny@ucc.ie.
  • McCowan LM; Department of Obstetrics and Gynaecology, University of Auckland, 2 Park Road, Auckland 1023, New Zealand. l.mccowan@auckland.ac.nz.
  • Baker PN; Liggins Institute, University of Auckland, 85 Park Road, Auckland 1023, New Zealand. philip.baker@auckland.ac.nz.
Int J Mol Sci ; 16(11): 27741-8, 2015 Nov 19.
Article en En | MEDLINE | ID: mdl-26610472
ABSTRACT
In our study, we used a mass spectrometry-based metabolomic approach to search for biomarkers that may act as early indicators of spontaneous preterm birth (sPTB). Samples were selected as a nested case-control study from the Screening for Pregnancy Endpoints (SCOPE) biobank in Auckland, New Zealand. Cervicovaginal swabs were collected at 20 weeks from women who were originally assessed as being at low risk of sPTB. Samples were analysed using gas chromatography-mass spectrometry (GC-MS). Despite the low amount of biomass (16-23 mg), 112 compounds were detected. Statistical analysis showed no significant correlations with sPTB. Comparison of reported infection and plasma inflammatory markers from early pregnancy showed two inflammatory markers were correlated with reported infection, but no correlation with any compounds in the metabolite profile was observed. We hypothesise that the lack of biomarkers of sPTB in the cervicovaginal fluid metabolome is simply because it lacks such markers in early pregnancy. We propose alternative biofluids be investigated for markers of sPTB. Our results lead us to call for greater scrutiny of previously published metabolomic data relating to biomarkers of sPTB in cervicovaginal fluids, as the use of small, high risk, or late pregnancy cohorts may identify metabolite biomarkers that are irrelevant for predicting risk in normal populations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vagina / Cuello del Útero / Líquido Extracelular / Nacimiento Prematuro / Metaboloma / Metabolómica Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Int J Mol Sci Año: 2015 Tipo del documento: Article País de afiliación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vagina / Cuello del Útero / Líquido Extracelular / Nacimiento Prematuro / Metaboloma / Metabolómica Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Int J Mol Sci Año: 2015 Tipo del documento: Article País de afiliación: Nueva Zelanda