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Issue 1022 coverCIRCULATING NUCLEIC ACIDS IN PLASMA/SERUM III AND SERUM PROTEOMICS Volume 1022 published June 2004
Ann. N.Y. Acad. Sci. 1022: 129–134 (2004). doi: 10.1196/annals.1318.021
Copyright © 2004 by the New York Academy of Sciences
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Articles by WATAGANARA, T.
Articles by BIANCHI, D. W.
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Articles by WATAGANARA, T.
Articles by BIANCHI, D. W.
Circulating Cell-Free Fetal Nucleic Acid Analysis May Be a Novel Marker of Fetomaternal Hemorrhage after Elective First-Trimester Termination of Pregnancy

TUANGSIT WATAGANARAa, ERIK S. LESHANEa, ANGELA Y. CHEN, LISA M. SULLIVANc, INGA PETERd, LYNN BORGATTAb, KIRBY L. JOHNSONa AND DIANA W. BIANCHIa

aDivision of Genetics, Departments of Pediatrics, Obstetrics and Gynecology, Tufts-New England Medical Center, Boston, Massachusetts, USA
bDepartment of Obstetrics and Gynecology, Boston Medical Center, Boston, Massachusetts, USA
cDepartment of Biostatistics, Boston University, Boston, Massachusetts, USA
dInstitute of Clinical Research and Health Policy Studies, Tufts-New England Medical Center, Boston, Massachusetts, USA

Address for correspondence: Diana W. Bianchi, MD, Tufts-New England Medical Center, Box 394, 750 Washington Street, Boston, MA 02111. Voice: 617-636-1468; fax: 617-636-1469. Dbianchi{at}tufts-nemc.org
Ann. N.Y. Acad. Sci. 1022: 129-134 (2004).

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 {gamma}-globin transcript as a marker of fetal erythroid cells. Although plasma {gamma}-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.

Key Words: fetal DNA • fetomaternal hemorrhage • therapeutic abortion • {gamma}-globin mRNA • fetal gene expression




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P. B. Larrabee, K. L. Johnson, I. Peter, and D. W. Bianchi
Presence of Filterable and Nonfilterable Cell-Free mRNA in Amniotic Fluid
Clin. Chem., June 1, 2005; 51(6): 1024 - 1026.
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