Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy 21

YMD Lo, TK Lau, J Zhang, TN Leung… - Clinical …, 1999 - academic.oup.com
YMD Lo, TK Lau, J Zhang, TN Leung, AMZ Chang, NM Hjelm, RS Elmes, DW Bianchi
Clinical chemistry, 1999academic.oup.com
Background: The recent discovery of the presence of circulating cell-free fetal DNA in
maternal plasma opens up new prenatal diagnostic applications and provides new avenues
for clinical investigation. It is of research and potential diagnostic interest to determine
whether fetal trisomy 21 may be associated with quantitative abnormalities of circulating fetal
DNA in maternal plasma. Methods: Maternal plasma samples were prospectively collected
from two centers situated in Hong Kong and Boston. Samples collected from Boston …
Abstract
Background: The recent discovery of the presence of circulating cell-free fetal DNA in maternal plasma opens up new prenatal diagnostic applications and provides new avenues for clinical investigation. It is of research and potential diagnostic interest to determine whether fetal trisomy 21 may be associated with quantitative abnormalities of circulating fetal DNA in maternal plasma.
Methods: Maternal plasma samples were prospectively collected from two centers situated in Hong Kong and Boston. Samples collected from Boston consisted of 7 women carrying male trisomy 21 fetuses, 19 carrying euploid male fetuses, and 13 carrying female fetuses. Samples collected from Hong Kong consisted of 6 women carrying male trisomy 21 fetuses, 18 carrying euploid male fetuses, and 10 carrying female fetuses. Male fetal DNA in maternal plasma was measured using real-time quantitative Y-chromosomal PCR.
Results: For patients recruited from Boston, the median circulating fetal DNA concentrations in women carrying trisomy 21 and euploid male fetuses were 46.0 genome-equivalents/mL and 23.3 genome-equivalents/mL, respectively (P = 0.028). For patients recruited from Hong Kong, the median circulating fetal DNA concentrations in women carrying trisomy 21 and euploid male fetuses were 48.2 genome-equivalents/mL and 16.3 genome-equivalents/mL, respectively (P = 0.026). None of the samples from women carrying female fetuses had detectable Y-chromosomal signals.
Conclusions: Abnormally high concentrations of circulating fetal DNA are found in a proportion of women carrying fetuses with trisomy 21. The robustness and reproducibility of real-time PCR analysis of maternal plasma makes it a valuable tool for cross-institutional collaboration involving centers located in different parts of the world.
Oxford University Press