Circulating noncoding RNAs as early predictive biomarkers in preeclampsia: a diagnostic meta-analysis

Reprod Biol Endocrinol. 2021 Dec 1;19(1):177. doi: 10.1186/s12958-021-00852-8.

Abstract

Background: We designed a meta-analysis to evaluate the clinical significance and efficacy of circulating noncoding RNAs (ncRNAs) in the early prediction of preeclampsia.

Methods: PubMed, Embase and the Cochrane Library were used to search for literature. The combined prediction performance was evaluated by calculating the area under the summary receiver operator characteristic (SROC) curve. The potential sources of heterogeneity were analysed by meta-regression analysis and subgroup analysis. All statistical analyses and mapping were performed by RevMan 5.3 and Stata 12.0.

Results: A total of 41 studies from 14 articles, including 557 preeclampsia patients and 842 controls, were included in our meta-analysis. All studies collected blood before onset. NcRNAs in blood performed relatively well in predicting preeclampsia. The combined sensitivity was 0.71, the specificity was 0.84, and the area under the SROC curve (AUC) was 0.86. Peripheral blood mononuclear cell (PBMC) samples showed the best diagnostic accuracy. The combined AUC was 0.93. Combined detection was better than single detection, and miRNA was better than circRNA. The heterogeneity of the study was determined by sample size, lncRNA characteristics, lncRNA source and race.

Conclusion: Circulating ncRNAs can be valuable biomarkers used as candidates for noninvasive early predictive biomarkers of preeclampsia and have great clinical application prospects. The clinical value of ncRNAs needs to be tested by further multicentre, comprehensive and prospective studies, and the test criteria should be established.

Keywords: Biomarkers; Diagnostic meta-analysis; Preeclampsia; ncRNAs.

Publication types

  • Meta-Analysis

MeSH terms

  • Biomarkers / blood
  • Cell-Free Nucleic Acids / blood*
  • Female
  • Humans
  • Pre-Eclampsia / blood
  • Pre-Eclampsia / diagnosis*
  • Pregnancy
  • RNA, Long Noncoding / blood*
  • Sensitivity and Specificity

Substances

  • Biomarkers
  • Cell-Free Nucleic Acids
  • RNA, Long Noncoding