Potential candidate maternal serum miRNAs for the diagnosis of fetal congenital heart disease

miRNA candidates for diagnosis of fetal CHD

Authors

  • Yimeng Xi Department of Ultrasound,Nanjing Maternity and Child Health Care Hospital, Women’s Hospital of Nanjing Medical University
  • Enkang Lu Department of Cardiothoracic Surgery,The First Affiliated Hospital of Nanjing Medical University
  • Xinyan Ruan The First School of Clinical Medicine,Nanjing Medical University
  • Ruoyun Wu School of Stomatology,Nanjing Medical University
  • Lijun Wu Department of Ultrasound,Nanjing Maternity and Child Health Care Hospital, Women’s Hospital of Nanjing Medical University
  • Ting Zhou Department of Ultrasound,Nanjing Maternity and Child Health Care Hospital, Women’s Hospital of Nanjing Medical University
  • Haitao Gu Central Laboratory of Jiangsu Provincial Maternal and Child Health Care Hospital, Maternal and Child Branch of the First Affiliated Hospital of Nanjing Medical University
  • Yun Wu Department of Cardiothoracic Surgery,The First Affiliated Hospital of Nanjing Medical University

Keywords:

congenital heart disease, prenatal detection, miRNAs, biomarker

Abstract

Congenital heart disease (CHD) is one of the most significant birth defects leading to infant mortality worldwide. Circulating microRNAs (miRNAs) are emerging as novel biomarkers for the detection of cardiovascular diseases. In this study, we aimed to investigate the role of maternal serum miRNAs expression as biomarkers in the diagnosis and prediction of children with CHD. High-throughput sequencing of peripheral blood from pregnant women with abnormal and normal fetal hearts identified 1939 differentially expressed miRNAs, the first 11 of which were selected as predictive biomarkers of CHD. The expression of miRNAs in more clinical samples was then quantitatively verified by reverse transcriptase polymerase chain reaction and the correlation between abnormal miRNAs and CHD was analyzed. Two miRNAs (hsa-miR-3195 and hsa-miR-122-5p) were found to be significantly down-regulated in pregnant women with fetal CHD. By further bioinformatics analysis, we predicted that hsa-miR-3195 and hsa-miR-122-5p could induce CHD by influencing biometabolic processes. hsa-miR-3195 and hsa-miR-122-5p may serve as novel non-invasive biomarkers for prenatal detection of fetal CHD.

Published

2024-10-06

Issue

Section

Original Research Articles