Maternal serum placental growth factor and α-fetoprotein testing in first trimester screening for Down syndrome

被引:31
作者
Donalson, Kim [1 ]
Turner, Steve [1 ]
Morrison, Lesley [1 ]
Liitti, Paivi [2 ]
Nilsson, Christel [3 ]
Cuckle, Howard [3 ]
机构
[1] Royal Victoria Infirm, Dept Biochem, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[2] Wallac Oy, FIN-20101 Turku, Finland
[3] Columbia Univ, Coll Med, New York, NY USA
关键词
BIOCHEMICAL MARKERS; WEEKS GESTATION; PREGNANCIES; TRISOMY-21; RISK; AGE;
D O I
10.1002/pd.4087
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective The aim of this research was to evaluate the addition of first trimester maternal serum placental growth factor (PlGF) and -fetoprotein (AFP) to the combined test for Down syndrome and a serum only protocol of PlGF, AFP, free -human chorionic gonadotropin and pregnancy-associated plasma protein-A. Methods Samples were from 92 Down syndrome cases with 552 matched controls. All women had a combined test at 1114weeks gestation. PlGF and AFP were measured and expressed in multiples of the gestation-specific median (MoM), adjusting for maternal weight and smoking status. Multivariate Gaussian modeling was used to predict detection and false-positive rates. Results The median PlGF level in the cases was 0.694 MoM and controls 1.000 MoM (p=<0.0001). The corresponding values for AFP were 0.764 MoM and 0.990 MoM (p<0.0001). Statistical modeling predicted that for a given false-positive rate, the addition of PlGF to the combined test increases the detection rate by 47%. For a given detection rate, the false-positive rate could be almost halved. When both PlGF and AFP are used, the detection rate increase is 58%. A serum only protocol had a predicted a detection rate of 71% for a false-positive rate of 5%. Conclusions Results suggest a substantial benefit of adding PlGF to the combined test. (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:457 / 461
页数:5
相关论文
共 16 条
[1]   Prediction of early, intermediate and late pre-eclampsia from maternal factors, biophysical and biochemical markers at 11-13 weeks [J].
Akolekar, Ranjit ;
Syngelaki, Argyro ;
Sarquis, Rita ;
Zvanca, Mona ;
Nicolaides, Kypros H. .
PRENATAL DIAGNOSIS, 2011, 31 (01) :66-74
[2]   Maternal Serum α-Fetoprotein at 11-13 Weeks' Gestation in Spontaneous Early Preterm Delivery [J].
Beta, Jarek ;
Bredaki, Foteini E. ;
Calvo, Jesus Rodriguez ;
Akolekar, Ranjit ;
Nicolaides, Kypros H. .
FETAL DIAGNOSIS AND THERAPY, 2011, 30 (02) :88-93
[3]   Stability of first trimester placental growth factor in serum and whole blood [J].
Cowans, N. J. ;
Alfthan, H. ;
Stenman, U. H. ;
Spencer, K. .
PRENATAL DIAGNOSIS, 2011, 31 (12) :1193-1197
[4]   First trimester maternal serum placental growth factor in trisomy 21 pregnancies [J].
Cowans, N. J. ;
Stamatopoulou, A. ;
Spencer, K. .
PRENATAL DIAGNOSIS, 2010, 30 (05) :449-453
[5]   Age-standardisation when target setting and auditing performance of Down syndrome screening programmes [J].
Cuckle, H ;
Aitken, D ;
Goodburn, S ;
Senior, B ;
Spencer, K ;
Standing, S .
PRENATAL DIAGNOSIS, 2004, 24 (11) :851-856
[6]   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
[7]  
Cuckle HS, 2010, GENETIC DISORDERS FE, P771
[8]  
Kagan K, 2012, ULTRASOUND OBSTET GY
[9]   Modeling Down syndrome screening performance using first-trimester serum markers [J].
Koster, M. P. H. ;
Wortelboer, E. J. ;
Stoutenbeek, P. ;
Visser, G. H. A. ;
Schielen, P. C. J. I. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2011, 38 (02) :134-139
[10]   Maternal Serum Placental Growth Factor in Prospective Screening for Aneuploidies at 8-13 Weeks' Gestation [J].
Pandya, Pranav ;
Wright, David ;
Syngelaki, Argyro ;
Akolekar, Ranjit ;
Nicolaides, Kypros H. .
FETAL DIAGNOSIS AND THERAPY, 2012, 31 (02) :87-93