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Circulating Cell-Free Fetal Nucleic Acid Analysis May Be a Novel Marker of Fetomaternal Hemorrhage after Elective First-Trimester Termination of Pregnancy

Authors :
Erik S. LeShane
Diana W. Bianchi
Lynn Borgatta
Kirby L. Johnson
Tuangsit Wataganara
Inga Peter
Angela Y. Chen
Lisa M. Sullivan
Source :
Annals of the New York Academy of Sciences. 1022:129-134
Publication Year :
2004
Publisher :
Wiley, 2004.

Abstract

Analysis of cell-free fetal DNA (fDNA) and RNA in maternal plasma could be useful in the diagnosis and management of complications of pregnancy. In this review, we discuss our studies to investigate the potential of fetal nucleic acid measurement in maternal plasma as a marker of fetomaternal hemorrhage (FMH) after elective first-trimester termination of pregnancy (TOP). Using quantitative real-time PCR amplification of the DYS1 sequence, elevation of plasma fDNA levels after TOP was observed, especially in the late first trimester. This corresponds with the functional development of the placental vascular structure and fetal hematopoiesis. This Y sequence-based PCR amplification assay, however, limits the analysis to pregnant women carrying male fetuses. Therefore, we also developed a real-time quantitative reverse-transcriptase PCR assay of the γ-globin transcript as a marker of fetal erythroid cells. Although plasma γ-globin mRNA levels were decreased after TOP in many patients, an elevation was observed in some patients at greater than 9 weeks' gestation, which is consistent with the increase in plasma fDNA levels. Our data suggest that fetal hematopoietic cells contribute to the pool of fetal nucleic acids in the maternal circulation. Measurement of cell-free fetal nucleic acid levels in maternal plasma may have clinical application as a novel marker of FMH after 9 weeks of gestation.

Details

ISSN :
17496632 and 00778923
Volume :
1022
Database :
OpenAIRE
Journal :
Annals of the New York Academy of Sciences
Accession number :
edsair.doi.dedup.....c6186d0449b316a254ca7f062823ebcc
Full Text :
https://doi.org/10.1196/annals.1318.021