Time-resolved immunofluorometric assay of pregnancy-associated plasma protein A in maternal serum screening for Down's syndrome in first trimester of pregnancy

被引:19
|
作者
Qin, QP
Nguyen, TH
Christiansen, M
Larsen, SO
NorgaardPedersen, B
机构
[1] STATENS SERUM INST, DEPT CLIN BIOCHEM, DK-2300 COPENHAGEN S, DENMARK
[2] UNIV COPENHAGEN, HERLEV HOSP, DEPT OBSTET & GYNAECOL, DK-1168 COPENHAGEN, DENMARK
[3] STATENS SERUM INST, DEPT BIOSTAT, DK-2300 COPENHAGEN S, DENMARK
关键词
pregnancy-associated plasma protein A; pregnancy; screening for Down's syndrome; time-resolved immunofluorescence; A PAPP-A; MAJOR BASIC-PROTEIN; FOLLICULAR-FLUID; FETAL TRISOMIES; 1ST TRIMESTER; RADIOIMMUNOASSAY; PROFORM; MARKERS;
D O I
10.1016/0009-8981(96)06378-4
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
A low maternal serum concentration of pregnancy associated plasma protein-A (MS-PAPP-A) in the first trimester has been suggested as a marker for the presence of a Down's syndrome (DS) fetus. We developed a time-resolved immunofluorometric assay (TrIFMA) for PAPP-A with a sensitivity < 3.9 mIU/I. In the 7-12 gestational weeks interval the median multiples of the median (MoM) was 0.57 (95%-confidence interval: 0.47-0.99) in DS pregnancies (n = 29) and lower than in controls (n = 223) (P < 0.005). The efficiency of MS-PAPP-A alone was evaluated using empirical receiver-operator-characteristics (ROC) and a sensitivity of about 25% was found for a false-positive rate of about 10% in the 7-12 gestational weeks interval. In parameterized ROC analysis a sensitivity of 9% was found for a false-positive rate of 5%. The TrIFMA PAPP-A assay seems to fulfil the quality criteria for an assay to be used in large-scale serum screening for Down's syndrome.
引用
收藏
页码:113 / 129
页数:17
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