Detection of cell-free fetal mRNA in maternal plasma for a new prenatal screening marker of Down's syndrome.
Weiwei Cheng, Xinrong Zhao, Hua Zhang, Yan Chen, Yanlin Wang
Abstract
Weiwei Cheng, Xinrong Zhao, Hua Zhang, Yan Chen, Yanlin Wang
Abstract
Objective Detection of cell-free fetal mRNA in maternal plasma by real-time quantitative flouorescence polymerase chain reaction(QF-PCR) and on the basis of it's amount to discuss the feasibility as a new prenatal screening indicator of Down'S syndrome. Methods Peripheral blood samples (n=26) were collected from pregnant women attending the International Peace Maternity and Child Health Hospital,School of Medicine,Shanghai Jiaotong University from May 2007 to August 2008.Cel1-free fetal mRNA in maternal plasma was isolated from 26 samples in the midtrimester(15~26W)pregnancy.Samples consisted of 9 women carrying trisomy 21 fetuses(group B),4 carrying aneuploid fetuses(group C),and 13 carrying normal fetuses(group A).QF-PCR was used to detect HPL,β-HCG,TFPI2,DSCR4,LOC90625 gene markers of the placental origin and 18sRNA gene of the mothers and the fetuses. Results All abnormal high concentrations of cell-free fetal mRNA but TFPI2 were found in a proportion of women carrying trisomy 21 fetuses and aneuploid fetuses(P0.01).Conclusion Cell-free fetal mRNA in maternal plasma is a potential prenatal screening maker for trisomy 21.
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Objective Detection of cell-free fetal mRNA in maternal plasma by real-time quantitative flouorescence polymerase chain reaction(QF-PCR) and on the basis of it's amount to discuss the feasibility as a new prenatal screening indicator of Down'S syndrome. Methods Peripheral blood samples (n=26) were collected from pregnant women attending the International Peace Maternity and Child Health Hospital,School of Medicine,Shanghai Jiaotong University from May 2007 to August 2008.Cel1-free fetal mRNA in maternal plasma was isolated from 26 samples in the midtrimester(15~26W)pregnancy.Samples consisted of 9 women carrying trisomy 21 fetuses(group B),4 carrying aneuploid fetuses(group C),and 13 carrying normal fetuses(group A).QF-PCR was used to detect HPL,β-HCG,TFPI2,DSCR4,LOC90625 gene markers of the placental origin and 18sRNA gene of the mothers and the fetuses. Results All abnormal high concentrations of cell-free fetal mRNA but TFPI2 were found in a proportion of women carrying trisomy 21 fetuses and aneuploid fetuses(P0.01).Conclusion Cell-free fetal mRNA in maternal plasma is a potential prenatal screening maker for trisomy 21.
Key concepts: Trisomy, Fetus, Cell-free fetal DNA, Prenatal diagnosis, Medicine, Down syndrome, Andrology, Pregnancy