Transcriptomic profile assessment for preeclampsia prediction and early diagnostics

Aim : to develop a model for predicting preeclampsia (PE) based on the clinically most significant differentially expressed plasma microRNAs. Materials and Methods . A prospective observational comparative study was conducted with 62 women, divided into two parallel groups: 32 patients with PE and 3...

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Veröffentlicht in:Акушерство, гинекология и репродукция гинекология и репродукция, 2024-07, Vol.18 (3), p.316-327
Hauptverfasser: Melnik, A. V., Solovyova, V. E., Yatsenko, Yu. O., Filippova, A. E., Asryan, E. G., Seitumerov, T. Е., Myshak, E. R., Chernysheva, Yu. A., Ziyadinova, S. A., Kononenko, V. O., Kadyrova, M. R., Denisenko, A. A., Ismagilova, K. T., Mushinsky, D. V., Sorokina, L. E.
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Sprache:eng ; rus
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Zusammenfassung:Aim : to develop a model for predicting preeclampsia (PE) based on the clinically most significant differentially expressed plasma microRNAs. Materials and Methods . A prospective observational comparative study was conducted with 62 women, divided into two parallel groups: 32 patients with PE and 30 clinically healthy women with uncomplicated pregnancy. Transcriptomic analysis was performed to identify differentially expressed blood plasma microRNAs using next generation sequencing (NGS). Results . Calculation of risk ratios for PE development allowed to identify 14 plasma microRNAs that influence the development of PE pathology. PE-associated microRNAs hsa-miR-103a-3p, hsa-miR-451a and hsa-miR-516a-5p have a high diagnostic value when combined to assess their blood plasma expression level in early pregnancy stages. Conclusion . The developed prognostic model can be applied to pregnant women at risk for PE development, which may further reduce obstetric complications and improve perinatal outcomes.
ISSN:2313-7347
2500-3194
DOI:10.17749/2313-7347/ob.gyn.rep.2024.521