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Prenatal sex determination from maternal peripheral blood using the polymerase chain reaction
Authors:Y. -M. Dennis Lo  Pushpa Patel  Colin N. Baigent  Michael D. G. Gillmer  Paul Chamberlain  Maurizio Travi  Maurizio Sampietro  James S. Wainscoat  Kenneth A. Fleming
Affiliation:(1) Nuffield Department of Pathology and Bacteriology, John Radcliffe Hospital, OX39DU Oxford, UK;(2) Department of Haematology, John Radcliffe Hospital, OX39DU Oxford, UK;(3) Clinical Trial Service Unit, Harkness Building, Radcliffe Infirmary, OX26HE Oxford, UK;(4) Maternity Department, John Radcliffe Hospital, OX39DU Oxford, UK;(5) Istituti Clinici di Perfezionamento, Milan, Italy;(6) Istituto di Medicina Interna e Fisiopatologia Medica, Universita di Milano, Milan, Italy
Abstract:We have investigated the use of a nested polymerase chain reaction assay for the detection of a fetal-specific Y-chromosomal sequence (DYS14) from DNA extracted from unsorted maternal peripheral blood. Serial dilutions of male DNA into female cord blood DNA indicated that the assay could detect an equivalent of a single male cell in 300000 female cells. The assay exhibited absolute specificity for male DNA with no amplification from a DNA panel obtained from 10 female cord blood samples. When used on DNA extracted from unsorted peripheral blood from a series of pregnant women, the predictive values of a positive test for a male fetus were 86%, 67% and 87% in the first, second and third trimesters, respectively. We have also demonstrated that retesting the samples allows the detection of a proportion of male-bearing pregnancies with a high degree of accuracy, in that all 15 women who gave positive signals in two consecutive amplifications had male fetuses. We have also applied the test at 8 weeks post-partum to eight women who had previously delivered male babies; no Y-specific signal could be detected in any of them, suggesting that most women have cleared their circulation of fetal cells by 8 weeks after parturition.
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