The time of appearance and disappearance of fetal DNA from the maternal circulation
- 1 July 1995
- journal article
- research article
- Published by Wiley in Prenatal Diagnosis
- Vol. 15 (7) , 641-646
- https://doi.org/10.1002/pd.1970150709
Abstract
A single copy Y‐chromosome DNA sequence was amplified using the polymerase chain reaction (PCR) from the peripheral blood of 30 women who had achieved a pregnancy through an in vitro fertilization (IVF) programme. The time of conception was known precisely and was confirmed by serial ultrasound scans. Conceptions were dated as the number of weeks after fertilization plus 2, to give a time equivalent to the obstetric menstrual dating of the pregnancy (LMP). Y‐chromosome‐specific DNA was detected in all pregnancies with a male fetus (18/30). The earliest detection was at 4 weeks and 5 days, and the latest at 7 weeks and 1 day. Y‐chromosome‐specific sequences were no longer detected in any of the male pregnancies 8 weeks after delivery. No Y‐chromosome sequences were detected in any of the pregnancies where only female babies were delivered. This demonstrates that fetal DNA appears in the maternal circulation early in the first trimester, that it can be identified in all pregnancies tested by 7 weeks, that it continues to be present throughout pregnancy, and that it has been cleared from the maternal circulation 2 months after parturition. Early non‐invasive prenatal diagnosis for aneuploidies and inherited disorders will be possible in all pregnancies if fetal cells can be isolated free from maternal contamination (or identified accurately in the presence of maternal cells) without problems of contamination from previous pregnancies.Keywords
This publication has 18 references indexed in Scilit:
- Y chromosome sequence DNA amplified from peripheral blood of women in early pregnancyThe Lancet, 1994
- Detection of Fetal Trisomies 21 and 18 From Maternal Blood Using Triple Gradient and Magnetic Cell SortingAmerican Journal of Reproductive Immunology, 1993
- Breaking the blood barrierNature Genetics, 1992
- Non‐invasive first trimester antenatal diagnosisBJOG: An International Journal of Obstetrics and Gynaecology, 1992
- Detection of 47, XYY Trophoblast Fetal Cells in Maternal Blood by Fluorescence in situ Hybridization after Using Immunomagnetic Lymphocyte Depletion and Flow Cytometry SortingFetal Diagnosis and Therapy, 1992
- Trophoblast-like cells sorted from peripheral maternal blood using flow cytometry: A multiparametric study involving transmission electron microscopy and fetal dna amplificationPrenatal Diagnosis, 1991
- Possible effect of gestational age on the detection of fetal nucleated erythrocytes in maternal bloodPrenatal Diagnosis, 1991
- PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOODThe Lancet, 1989
- Chimaerism following allogeneic bone marrow transplantation: detection of residual host cells using the polymerase chain reactionBritish Journal of Haematology, 1989
- GENE AMPLIFICATION TO DETECT FETAL NUCLEATED CELLS IN PREGNANT WOMENThe Lancet, 1989