Large-scale pre-diagnosis study of fetal RHD genotyping by PCR on plasma DNA from RhD-negative pregnant women

Mol Diagn. 2004;8(1):23-31. doi: 10.1007/BF03260044.

Abstract

Background: The routine prenatal determination of fetal RhD blood group would be very useful in the management of pregnancies in RhD-negative women, as up to 40% of these pregnancies bear a RhD-negative fetus. The fetal DNA present in maternal plasma offers an opportunity for risk-free prenatal diagnosis.

Aim: This study focused on the feasibility and accuracy of large-scale RhD fetal diagnosis in non-immunized and anti-D immunized RhD-negative women.

Methods: Plasma DNA was extracted from 893 RhD-negative pregnant women and amplified in exons 7 and 10 of the RHD gene using conventional and real-time PCR. The results were then compared with the RHD fetal genotype determined on amniotic cells and/or the RhD phenotype of the red blood cells of the infants at birth.

Results: After exclusion of 42 samples from women exhibiting a nonfunctional or rearranged RHD gene, fetal RhD status was predicted with a 99.5% accuracy. A strategy is also proposed to avoid the small number of false-positive and -negative results.

Conclusion: Fetal RHD genotyping from maternal plasma DNA in different clinical situations may be used with confidence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA / blood*
  • DNA / genetics*
  • Diagnostic Errors
  • Erythroblastosis, Fetal / blood
  • Erythroblastosis, Fetal / diagnosis
  • Erythroblastosis, Fetal / genetics
  • Exons
  • Female
  • Fetal Blood / immunology*
  • Genotype
  • Humans
  • Infant, Newborn
  • Introns
  • Male
  • Polymerase Chain Reaction
  • Pregnancy
  • Prenatal Diagnosis
  • Rh-Hr Blood-Group System / genetics*

Substances

  • Rh-Hr Blood-Group System
  • Rho(D) antigen
  • DNA