Screening for Down's syndrome in early and late first and second trimester using six maternal serum markers

被引:15
作者
Christiansen, M
Larsen, SO
Oxvig, C
Qin, QP
Wagner, JM
Overgaard, MT
Gleich, GJ
Sottrup-Jensen, L
Norgaard-Pedersen, B
机构
[1] Statens Serum Inst, Dept Clin Biochem, DK-2300 Copenhagen S, Denmark
[2] Statens Serum Inst, Dept Biostat, DK-2300 Copenhagen, Denmark
[3] Aarhus Univ, Dept Mol Biol, DK-8000 Aarhus, Denmark
[4] Mayo Clin & Mayo Fdn, Dept Immunol & Med, Rochester, NY USA
关键词
AFP; chromosome disease; first trimester; hCG; nuchal translucency; PAPP-A; prenatal diagnosis; ProMBP; screening; SP1;
D O I
10.1111/j..2004.00177.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The efficiency of six maternal serum markers for Down's syndrome (DS), alpha fetoprotein (AFP), human chorionic gonadotropin (hCG), free beta-hCG, pregnancy-associated plasma protein-A (PAPP-A), the proform of eosinophil major basic protein (ProMBP), pregnancy-specific-beta-1-glycoprotein (SP1), and combinations thereof, was examined. Discriminant analysis in 156 DS pregnancies and 546 controls defined three effective combinations of serum marker logMoMs (multiples of the median in control samples) in three gestational age windows, i.e. Index I (weeks 7-9) = 0.52 logMoM ProMBP + 0.28 logMoM PAPP-A - logMoM SP1; Index II (weeks 10-12) = 1.94 logMoM free beta-hCG - logMoM SP1, and Index III (weeks 15-19) = 0.78 logMoM free beta-hCG + 1.12 logMoM ProMBP - logMoM AFP. The estimated detection rates of indices and age for a false-positive rate (FPR) of 5% were 73% for Index I, 69% for Index II, and 60% for Index III. Including the ultrasound marker nuchal translucency, using a DS at term risk of 1 : 400 as cut-off, the detection rates of the indices increased to 86, 83, and 82% for FPRs of 4.3, 4.1, and 5.8%, respectively. The indices are promising markers for screening for DS.
引用
收藏
页码:11 / 16
页数:6
相关论文
共 39 条
[1]   1ST-TRIMESTER BIOCHEMICAL SCREENING FOR FETAL CHROMOSOME-ABNORMALITIES AND NEURAL-TUBE DEFECTS [J].
AITKEN, DA ;
MCCAW, G ;
CROSSLEY, JA ;
BERRY, E ;
CONNOR, JM ;
SPENCER, K ;
MACRI, JN .
PRENATAL DIAGNOSIS, 1993, 13 (08) :681-689
[2]   First trimester screening for Down's syndrome using maternal serum PAPP-A and free β-hCG in combination with fetal nuchal translucency thickness [J].
Biagiotti, R ;
Brizzi, L ;
Periti, E ;
d'Agata, A ;
Vanzi, E ;
Cariati, E .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1998, 105 (08) :917-920
[3]   LOW MATERNAL SERUM LEVELS OF PREGNANCY ASSOCIATED PLASMA PROTEIN-A (PAPP-A) IN THE 1ST TRIMESTER IN ASSOCIATION WITH ABNORMAL FETAL KARYOTYPE [J].
BRAMBATI, B ;
MACINTOSH, MCM ;
TEISNER, B ;
MAGUINESS, S ;
SHRIMANKER, K ;
LANZANI, A ;
BONACCHI, I ;
TULUI, L ;
CHARD, T ;
GRUDZINSKAS, JG .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1993, 100 (04) :324-326
[4]  
Christiansen M, 1999, PRENATAL DIAG, V19, P905, DOI 10.1002/(SICI)1097-0223(199910)19:10<905::AID-PD658>3.0.CO
[5]  
2-Q
[6]   An increase in cost-effectiveness of first trimester maternal screening programmes for fetal chromosome anomalies is obtained by contingent testing [J].
Christiansen, M ;
Larsen, SO .
PRENATAL DIAGNOSIS, 2002, 22 (06) :482-486
[7]  
CHRISTIANSEN M, 1997, SCREENING DOWNS SYND, P148
[8]  
CUCKLE H, 1996, EARLY HUM DEV, V47, P27
[9]  
Cuckle HS, 1999, PRENATAL DIAG, V19, P505, DOI 10.1002/(SICI)1097-0223(199906)19:6<505::AID-PD572>3.0.CO
[10]  
2-6