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Earliest gestational age for fetal sexing in cell‐free maternal plasma
Author(s) -
Rijnders R. J. P.,
Van Der Luijt R. B.,
Peters E. D. J.,
Goeree J. K.,
Van Der Schoot C. E.,
Ploos Van Amstel J. K.,
Christiaens G. C. M. L.
Publication year - 2003
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.750
Subject(s) - testis determining factor , sexing , fetus , cell free fetal dna , gestational age , obstetrics , pregnancy , gestation , medicine , y chromosome , prenatal diagnosis , andrology , biology , genetics , gene
Objectives To evaluate at what gestational age fetal DNA can reliably be detected at the earliest in maternal plasma. Methods We performed consecutive blood sampling in the first trimester of pregnancy in 17 women who were pregnant after in vitro fertilization (IVF) or intrauterine insemination (IUI). DNA was isolated and the Y‐chromosome specific SRY was amplified by real‐time polymerase chain reaction (PCR). We likewise studied 31 women prior to invasive prenatal diagnosis procedures for test validation purposes. All test results were compared to cytogenetic sex or sex at birth. Results The earliest SRY detection was at a gestational age of 5 weeks and 2 days. In none of 4 pregnancies ending in a miscarriage was SRY detected. We detected SRY in maternal plasma in 1 of 2 patients (50%) carrying a male fetus at a gestational age of 5 weeks, in 4 of 5 (80%) at a gestational age of 7 weeks, in 4 of 4 (100%) at a gestational age of 9 weeks. In all 7 women pregnant with a male fetus, the correct fetal sex was detected by 10 weeks. In none of the 6 patients who delivered a girl was SRY detected. In the validation group, SRY was detected in 13 of the 13 male, and none of the 18 female fetuses. Conclusions We conclude that real‐time PCR of the SRY gene promises to be a reliable technique for early fetal sexing in maternal plasma. Copyright © 2003 John Wiley & Sons, Ltd.

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