Human placental lactogen is a first-trimester maternal serum marker of Down syndrome

被引:12
作者
Christiansen, Michael [1 ]
Sorensen, Tina Lindvig [1 ]
Norgaard-Pedersen, Bent [1 ]
机构
[1] Statens Serum Inst, Dept Clin Biochem, DK-2300 Copenhagen S, Denmark
关键词
human chorionic somatotropin; hCS; hPL; prenatal screening; first trimester;
D O I
10.1002/pd.1600
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Human placental lactogen (hPL) is synthesised by the placenta and found in maternal serum. We analysed the potential of hPL as a first-trimester maternal serum-screening marker for fetal Down syndrome (DS). Materials and Methods hPL was quantified by ELISA in 47 DS pregnancies and 136 controls in gestational weeks 8-13. Distributions of log multiples of the median (MoMs) were established. The quantity of hPL in DS screening was estimated using Monte Carlo simulation methods. Results The mean log 10 MoM hPL was -0.1995 (SD: 0.1993) in affected and 0.0026 (SD: 0.2129) in control pregnancies. This corresponds to a MoM of 0.63 in DS pregnancies. hPL correlated significantly with log10 MoM values of hCG (r = 0.320) and PAPP-A (r = 0.590) in controls, but not with hCGP (r = 0.228) or PAPP-A (r = 0.090) in DS pregnancies. The inclusion of hPL in the double test (PAPP-A + hCGP) increased the detection rate from 67 to 75% for a false-positive rate of 5%. Conclusion hPL is a DS screening marker that is applicable at weeks 9-13 and could be included in multiple marker first-trimester screening for DS. Copyright (C) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:1 / 5
页数:5
相关论文
共 25 条
[1]  
BARRERASALDANA HA, 1983, J BIOL CHEM, V258, P3787
[2]   Practical strategies in contingent sequential screening for Down syndrome [J].
Benn, P ;
Wright, D ;
Cuckle, H .
PRENATAL DIAGNOSIS, 2005, 25 (08) :645-652
[3]  
Christiansen M, 1999, PRENATAL DIAG, V19, P905, DOI 10.1002/(SICI)1097-0223(199910)19:10<905::AID-PD658>3.0.CO
[4]  
2-Q
[5]   Inhibin A is a maternal serum marker for Down's syndrome early in the first trimester [J].
Christiansen, M ;
Norgaard-Pedersen, B .
CLINICAL GENETICS, 2005, 68 (01) :35-39
[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]   ESTIMATING A WOMANS RISK OF HAVING A PREGNANCY ASSOCIATED WITH DOWNS-SYNDROME USING HER AGE AND SERUM ALPHA-FETOPROTEIN LEVEL [J].
CUCKLE, HS ;
WALD, NJ ;
THOMPSON, SG .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1987, 94 (05) :387-402
[8]   Defect of villous cytotrophoblast differentiation into syncytiotrophoblast in Down's syndrome [J].
Frendo, JL ;
Vidaud, M ;
Guibourdenche, J ;
Luton, D ;
Muller, F ;
Bellet, D ;
Giovagrandi, Y ;
Tarrade, A ;
Porquet, D ;
Blot, P ;
Evain-Brion, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (10) :3700-3707
[9]   IMMUNOELECTRON MICROSCOPE OBSERVATIONS ON SECRETION OF HUMAN PLACENTAL-LACTOGEN (HPL) IN THE HUMAN CHORIONIC VILLI [J].
FUJIMOTO, S ;
HAMASAKI, K ;
UEDA, H ;
KAGAWA, H .
ANATOMICAL RECORD, 1986, 216 (01) :68-72
[10]   CHORIONIC GROWTH HORMONE-PROLACTIN (CGP) - SECRETION DISPOSITION BIOLOGIC ACTIVITY IN MAN AND POSTULATED FUNCTION AS GROWTH HORMONE OF 2ND HALF OF PREGNANCY [J].
GRUMBACH, MM ;
KAPLAN, SL ;
SCIARRA, JJ ;
BURR, IM .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1968, 148 (A2) :501-+