Replicate real-time PCR testing of DNA in maternal plasma increases the sensitivity of non-invasive fetal sex determination

被引:57
作者
Hromadnikova, I
Houbova, B
Hridelova, D
Voslarova, S
Kofer, J
Komrska, V
Habart, D
机构
[1] Univ Hosp Motol, Fac Med 2, Clin Paediat 2, Prague 15018 5, Czech Republic
[2] Masaryk Hosp, Dept Med Genet, Usti Nad Labem, Czech Republic
[3] Inst Hematol & Blood Transfus, Haemophilia Ctr, Prague, Czech Republic
关键词
fetal DNA; fetal gender; maternal plasma; real-time PCR; SRY gene;
D O I
10.1002/pd.556
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background We determined fetal sex in pregnancies referred for invasive prenatal diagnosis procedures by analysis of DNA in maternal plasma. Methods Twelve pregnancies at risk of X-linked haemophilia and 32 pregnancies at risk of chromosomal aneuploidies at a gestational age ranging from 10 to 18 weeks recruited before chorionic villus sampling or amniocentesis were involved in the study. Male fetal DNA in maternal plasma was detected by using real-time polymerase chain reaction with the SRY gene as a marker. Results The specificity of the system reached 100% (no Y signal was detected in 17 women pregnant with a female fetus) and the sensitivity reached 100% (SRY amplification in 27 examined samples). Conclusions Amplification of free fetal DNA in maternal plasma is a valid and rapid technique for predicting fetal sex in first- and second-trimester pregnancies and could allow the restriction of invasive sampling procedures to male fetuses at risk of X-linked disorders. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:235 / 238
页数:4
相关论文
共 15 条
[1]  
Bianchi DW, 1998, J PERINAT MED, V26, P175
[2]   First-trimester fetal sex determination in maternal serum using real-time PCR [J].
Costa, JM ;
Benachi, A ;
Gautier, E ;
Jouannic, JM ;
Ernault, P ;
Dumez, Y .
PRENATAL DIAGNOSIS, 2001, 21 (12) :1070-1074
[3]   Detection of fetal RHD-specific sequences in maternal plasma [J].
Faas, BHW ;
Beuling, EA ;
Christiaens, GCML ;
von dem Borne, AEGK ;
van der Schoot, CE .
LANCET, 1998, 352 (9135) :1196-1196
[4]  
Hahn S, 2000, ANN NY ACAD SCI, V906, P148
[5]   Fetal cells in maternal blood: current and future perspectives [J].
Hahn, S ;
Sant, R ;
Holzgreve, W .
MOLECULAR HUMAN REPRODUCTION, 1998, 4 (06) :515-521
[6]   Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum [J].
Honda, H ;
Miharu, N ;
Ohashi, Y ;
Samura, O ;
Kinutani, M ;
Hara, T ;
Ohama, K .
HUMAN GENETICS, 2002, 110 (01) :75-79
[7]   Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis [J].
Lo, YMD ;
Tein, MSC ;
Lau, TK ;
Haines, CJ ;
Leung, TN ;
Poon, PMK ;
Wainscoat, JS ;
Johnson, PJ ;
Chang, AMZ ;
Hjelm, NM .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) :768-775
[8]   Presence of fetal DNA in maternal plasma and serum [J].
Lo, YMD ;
Corbetta, N ;
Chamberlain, PF ;
Rai, V ;
Sargent, IL ;
Redman, CWG ;
Wainscoat, JS .
LANCET, 1997, 350 (9076) :485-487
[9]   Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma [J].
Lo, YMD ;
Hjelm, NM ;
Fidler, C ;
Sargent, IL ;
Murphy, MF ;
Chamberlain, PF ;
Poon, PMK ;
Redman, CWG ;
Wainscoat, JS .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (24) :1734-1738
[10]   Circulating fetal DNA in maternal plasma [J].
Poon, LLM ;
Lo, YMD .
CLINICA CHIMICA ACTA, 2001, 313 (1-2) :151-155