Wald Nicholas J, Bestwick Jonathan P, Morris Joan K
Department of Environmental and Preventive Medicine, Wolfson Institute of Preventive Medicine, Barts and the London Queen Mary's School of Medicine and Dentistry, UK.
Prenat Diagn. 2006 Jun;26(6):514-23. doi: 10.1002/pd.1446.
To examine the performance of Integrated Down syndrome screening (first- and second-trimester measurements integrated into a single screening test) when ratios of the levels of the same serum markers measured in both these trimesters (cross-trimester ratios) are added as new screening markers.
Using data from Serum Urine and Ultrasound Screening Study (SURUSS), second-trimester concentrations (in multiples of the median, or MoM) of pregnancy associated plasma protein A (PAPP-A), alphafetoprotein (AFP), unconjugated oestriol (uE(3)), human chorionic gonadotrophin (hCG) (free beta and total), and inhibin-A were divided by the first-trimester concentration to obtain a cross-trimester (CT) ratio for each analyte in 74 Down syndrome and 492 unaffected pregnancies. We identified CT ratios that improved screening performance and then, using Monte Carlo simulations, estimated the efficacy and cost effectiveness of adding them to the Integrated and serum Integrated tests.
All the median CT ratios differed significantly between Down syndrome and unaffected pregnancies. Setting the Integrated test to achieve a 90% detection rate, the false-positive rate (FPR) was 0.7% with CT ratios for PAPP-A, uE(3), inhibin-A, and total hCG compared with 2.2% without CT ratios, a reduction of about two-thirds. Using the serum Integrated test to achieve the same 90% detection rate and the first-trimester measurements made at 11 completed weeks of pregnancy, the corresponding FPRs were 2.4 and 8.1%, a similar proportional reduction. The AFP CT ratio had little effect on screening performance. Using CT ratios did not increase the cost per Down syndrome pregnancy detected.
The addition of CT ratios to an Integrated test substantially improves the efficacy and safety of prenatal screening for Down syndrome. It is cost effective and could be usefully introduced into screening programmes.
探讨将孕早期和孕中期测量结果整合为单一筛查试验的综合唐氏综合征筛查(Integrated Down syndrome screening)在添加两个孕期测量的相同血清标志物水平比值(跨孕期比值)作为新的筛查标志物时的表现。
利用血清、尿液和超声筛查研究(SURUSS)的数据,将孕中期妊娠相关血浆蛋白A(PAPP-A)、甲胎蛋白(AFP)、非结合雌三醇(uE₃)、人绒毛膜促性腺激素(hCG)(游离β亚基和总hCG)以及抑制素A的浓度(以中位数倍数,即MoM表示)除以孕早期浓度,得出74例唐氏综合征妊娠和492例正常妊娠中每种分析物的跨孕期(CT)比值。我们确定了能改善筛查表现的CT比值,然后通过蒙特卡洛模拟估计将这些比值添加到综合筛查试验和血清综合筛查试验中的效果及成本效益。
唐氏综合征妊娠和正常妊娠之间所有CT比值中位数均存在显著差异。设定综合筛查试验的检出率为90%时,使用PAPP-A、uE₃、抑制素A和总hCG的CT比值时假阳性率(FPR)为0.7%,而不使用CT比值时为2.2%,降低了约三分之二。使用血清综合筛查试验达到相同的90%检出率且孕早期测量在妊娠11整周时进行,相应的FPR分别为2.4%和8.1%,比例降低相似。AFP的CT比值对筛查表现影响不大。使用CT比值并未增加每例检测出的唐氏综合征妊娠的成本。
在综合筛查试验中添加CT比值可显著提高唐氏综合征产前筛查的效果和安全性。其具有成本效益,可有效引入筛查项目。