Kinetics of SRY gene appearance in maternal serum:: detection by real time PCR in early pregnancy after assisted reproductive technique

被引:80
作者
Guibert, J
Benachi, A
Grebille, AG
Ernault, P
Zorn, JR
Costa, JM
机构
[1] Amer Hosp Paris, Ctr Diagnost Prenatal, F-92200 Neuilly, France
[2] Hop Cochin, Unite Assistance Med Procreat, F-75014 Paris, France
[3] Univ Paris 05, AP HP, Hop Necker Enfants Malad, F-75015 Paris, France
关键词
assisted reproduction; fetal DNA; maternal serum; pregnancy;
D O I
10.1093/humrep/deg320
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Fetal DNA circulating in maternal serum offers a possibility for non-invasive prenatal diagnosis but its kinetics during very early pregnancy is still unclear. In order to clarify this point, the studies on the kinetics of fetal DNA appearance in maternal serum were conducted on patients undergoing assisted reproduction. METHODS: Using a quantitative real time PCR assay, the presence of SRY gene sequences was evaluated in the serum of patients at the onset of pregnancy. RESULTS: Twenty-seven patients were originally studied but first trimester abortion occurred in five cases. Among the 22 ongoing pregnancies, ten were found to bear at least one male fetus and all sera from these women gave positive results for SRY gene detection. The SRY gene was found to be detectable as soon as day 18 after embryo transfer in one case and it had been found in the other nine patients by day 37. CONCLUSIONS: Fetal DNA is found in maternal serum even before the fetal circulation is established, which is highly suggestive that it is released, at least in part, from the trophoblast. Detection of fetal DNA in maternal serum very early in pregnancy may have clinical implications such as with the management of pregnant women carrying a fetus at risk for congenital adrenal hyperplasia.
引用
收藏
页码:1733 / 1736
页数:4
相关论文
共 14 条
[1]  
BENIRSCHKE K, 2000, PATHOLOGY HUMAN PLAC, P42
[2]   PRENATAL-DIAGNOSIS BY ANALYSIS OF FETAL CELLS IN MATERNAL BLOOD [J].
BIANCHI, DW .
JOURNAL OF PEDIATRICS, 1995, 127 (06) :847-856
[3]  
Chiu RWK, 2002, CLIN CHEM, V48, P778
[4]   Fetal RHD genotyping in maternal serum during the first trimester of pregnancy [J].
Costa, JM ;
Giovangrandi, Y ;
Ernault, P ;
Lohmann, L ;
Nataf, V ;
El Halali, N ;
Gautier, E .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 119 (01) :255-260
[5]   New strategy for prenatal diagnosis of X-linked disorders. [J].
Costa, JM ;
Benachi, A ;
Gautier, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (19) :1502-1502
[6]  
Costa JM, 2002, CLIN CHEM, V48, P679
[7]   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
[8]  
DEMIR R, 1989, ACTA ANAT, V136, P190
[9]   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
[10]   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