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Maternal Plasma miRNAs as Early Biomarkers of Moderate-to-Late-Preterm Birth.
Ramzan, Farha; Rong, Jing; Roberts, Claire T; O'Sullivan, Justin M; Perry, Jo K; Taylor, Rennae; McCowan, Lesley; Vickers, Mark H.
Afiliación
  • Ramzan F; Liggins Institute, University of Auckland, Auckland 1142, New Zealand.
  • Rong J; Liggins Institute, University of Auckland, Auckland 1142, New Zealand.
  • Roberts CT; Flinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide 5001, Australia.
  • O'Sullivan JM; Liggins Institute, University of Auckland, Auckland 1142, New Zealand.
  • Perry JK; Maurice Wilkins Centre, University of Auckland, Auckland 1142, New Zealand.
  • Taylor R; Liggins Institute, University of Auckland, Auckland 1142, New Zealand.
  • McCowan L; Maurice Wilkins Centre, University of Auckland, Auckland 1142, New Zealand.
  • Vickers MH; Department of Obstetrics and Gynaecology, Faculty of Medical and Health Science, University of Auckland, Auckland 1142, New Zealand.
Int J Mol Sci ; 25(17)2024 Sep 02.
Article en En | MEDLINE | ID: mdl-39273483
ABSTRACT
Globally, preterm birth (PTB) is a primary cause of mortality and morbidity in infants, with PTB rates increasing worldwide over the last two decades. Biomarkers for accurate early prediction of PTB before the clinical event do not currently exist. Given their roles in the development and progression of many disease states, there has been increasing interest in the utility of microRNAs (miRNAs) as early biomarkers for pregnancy-related disorders, including PTB. The present study was designed to examine potential differences in miRNA abundances in maternal plasma from mothers with infants born following a moderate to late (28-36 weeks' gestation, n = 54) spontaneous PTB (SPTB) compared to mothers with matched term infants (n = 54). Maternal plasma collected at 15 weeks' gestation were utilised from the Auckland and Adelaide cohorts from the Screening for Pregnancy Endpoints (SCOPE) study. miRNAs in plasma were quantified using the NanoString nCounter expression panel (800 miRNAs). The top four most abundant miRNAs were significantly decreased in the plasma of mothers in the SPTB group with results consistent across both cohorts and pathway analysis was undertaken to examine the biological processes linked to the dysregulated miRNAs. The top candidate miRNAs (miRs-451a, -223-3p, let-7a-5p, and -126-3p) were linked to gene pathways associated with inflammation, apoptosis, and mitochondrial biogenesis. Moreover, miRNAs were consistently less abundant in the plasma of mothers of preterm infants across both sites, suggesting potential global dysregulation in miRNA biogenesis. This was supported by a significant downregulation in expression of key genes that are involved in miRNA biogenesis (DROSHA, DICER, and AGO2) across both sites in the SPTB group. In summary, the present study has identified miRNAs in maternal plasma that may provide predictive utility as early biomarkers for the risk of later SPTB. Importantly, these observations were conserved across two independent cohorts. Further, our data provide evidence for a persistent decrease in miRNA abundance in mothers who later experienced an SPTB, which is likely to have widespread consequences for gene regulation and epigenetic processes.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / MicroARNs / Nacimiento Prematuro Límite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Nueva Zelanda Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / MicroARNs / Nacimiento Prematuro Límite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Nueva Zelanda Pais de publicación: Suiza