MicroRNAs in Fetal Umbilical Cord Blood as a Prenatal Screening Tool for Congenital Heart Disease

被引:1
作者
Kong, Dexuan [1 ]
Li, Huidong [1 ]
Ren, Chenchun [2 ]
Yang, Weiwei [2 ]
Zhang, Zhikun [1 ]
机构
[1] Tianjin Cent Hosp Gynecol Obstet, Dept Ultrasound, 156 Nankai Sanma Rd, Tianjin 300100, Peoples R China
[2] Tianjin Cent Hosp Gynecol Obstet, Dept Med Genet, Tianjin, Peoples R China
关键词
MicroRNAs; biomarkers; congenital heart disease; fetuses; diagnosis; prenatal screening; NONINVASIVE BIOMARKERS; CIRCULATING MICRORNAS; GENE-EXPRESSION; IDENTIFICATION; PROLIFERATION; PREDICTOR; SERUM;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objective. MicroRNAs (miRNAs) have been used as molecular markers for various diseases. This study aimed to evaluate the predicted performance of miRNAs in fetal umbilical cord blood for detecting congenital heart disease (CHD). Methods. In this retrospective cohort study, a total of 60 pregnant women (involving 30 fetuses with CHD and 30 normal fetuses requiring induction of labor) were included. Umbilical cord blood was collected for miRNA measurement. Expression levels of the miRNAs were detected by qRT-PCR. The predictive accuracy of miRNA was assessed by constructing a receiver operating characteristic (ROC) curve and evaluated by calculating the area under the curve (AUC). The point biserial correlation coefficient (PBCC) was analyzed to evaluate the correlation of miRNA with CHD. Results. The CHD group and control group were well-balanced in age, gravidity, and parity. miRNA-133 was not detected in all subjects. Subjects with CHD fetuses had significantly lower levels of miRNA-1, miRNA-208, and miRNA-499. Different types of CHD showed different variation trends of miRNA expression. Correlation analysis showed that expression levels of miRNA-1, miRNA-208, and miRNA-499 were negatively correlated with the occurrence of CHD, with a PBCC of -0.65, -0.47, and -0.60, respectively. miRNA-1, miRNA-208, and miRNA-499 displayed an AUC of 0.86 (95% CI, 0.76-0.96; p<0.001), 0.75 (95% CI, 0.63-0.87; p=0.009), and 0.84 (95% CI, 0.74-0.95; p<0.001), respectively, for discriminating CHD from normal fetuses, with cut-off values of 0.795, 0.835, and 0.795, respectively. Conclusion. The expression levels of miRNA-1, miRNA-208, and miRNA-499 in umbilical cord blood may be useful for predicting fetal CHD. The findings indicated that miRNAs have the potential to be a prenatal screening tool in the early diagnosis of CHD.
引用
收藏
页码:705 / 712
页数:8
相关论文
共 50 条
[31]   The pregnancy experience of Korean mothers with a prenatal fetal diagnosis of congenital heart disease [J].
Im, Yu-Mi ;
Yun, Tae-Jin ;
Yoo, Il-Young ;
Kim, Sanghee ;
Jin, Juhye ;
Kim, Sue .
BMC PREGNANCY AND CHILDBIRTH, 2018, 18
[32]   Prenatal detection rates for congenital heart disease using abnormal obstetrical screening ultrasound alone as indication for fetal echocardiography [J].
Vepa, Sanjay ;
Alavi, Mubarika ;
Wu, Weilu ;
Schmittdiel, Julie ;
Herrinton, Lisa J. ;
Desai, Kavin .
PRENATAL DIAGNOSIS, 2024, 44 (6-7) :706-716
[33]   Associations Between the Lead Level in Maternal Blood and Umbilical Cord Blood and Congenital Heart Diseases in Offspring [J].
Lei Huang ;
Baohong Mao ;
Jiayue Li ;
Nan Nan ;
Li He ;
Jie Qiu ;
Bin Yi ;
Qing Liu .
Biological Trace Element Research, 2023, 201 :2191-2199
[34]   Associations Between the Lead Level in Maternal Blood and Umbilical Cord Blood and Congenital Heart Diseases in Offspring [J].
Huang, Lei ;
Mao, Baohong ;
Li, Jiayue ;
Nan, Nan ;
He, Li ;
Qiu, Jie ;
Yi, Bin ;
Liu, Qing .
BIOLOGICAL TRACE ELEMENT RESEARCH, 2022, 201 (5) :2191-2199
[35]   Comparison of cardiac Z-score with cardiac asymmetry for prenatal screening of congenital heart disease [J].
Riggs, T. ;
Saini, A. P. ;
Comstock, C. H. ;
Lee, W. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2011, 38 (03) :332-336
[36]   Application of the 3-Vessel View in Routine Prenatal Sonographic Screening for Congenital Heart Disease [J].
Wu, Qingqing ;
Li, Man ;
Ju, Lirong ;
Zhang, Weiyuan ;
Yang, Xinghua ;
Yan, Yuxiang ;
Wang, Wei .
JOURNAL OF ULTRASOUND IN MEDICINE, 2009, 28 (10) :1319-1324
[37]   Integration of Prenatal Cardiovascular Magnetic Resonance Imaging in Congenital Heart Disease [J].
Desmond, Angela ;
Nguyen, Kim-Lien ;
Watterson, Christopher T. ;
Sklansky, Mark ;
Satou, Gary M. ;
Prosper, Ashley E. ;
Garg, Meena ;
Van Arsdell, Glen S. ;
Finn, J. Paul ;
Afshar, Yalda .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2023, 12 (22)
[38]   Fetal Brain Development in Congenital Heart Disease [J].
Peyvandi, Shabnam ;
Rollins, Caitlin .
CANADIAN JOURNAL OF CARDIOLOGY, 2023, 39 (02) :115-122
[39]   Maternal obesity alters C19MC microRNAs expression profile in fetal umbilical cord blood [J].
Jia Jing ;
Yingjin Wang ;
Yanmei Quan ;
Zhijie Wang ;
Yue Liu ;
Zhide Ding .
Nutrition & Metabolism, 17
[40]   Advancing Prenatal Detection of Congenital Heart Disease A Novel Screening Protocol Improves Early Diagnosis of Complex Congenital Heart Disease [J].
Letourneau, Karen M. ;
Horne, David ;
Soni, Reeni N. ;
McDonald, Keith R. ;
Karlicki, Fern C. ;
Fransoo, Randy R. .
JOURNAL OF ULTRASOUND IN MEDICINE, 2018, 37 (05) :1073-1079