Suresh Seshandri, Cuckle Howard S, Jagadeesh Sujatha, Ghosh Kushagradhi, Vemavarapu Gayathri, Taval Tulika, Suresh Sudarshan
1Mediscan Systems & Fetal Care Research Foundation, 197 Dr Natesan Road, Mylapore, Chennai, 600004 India.
2Department of Obstetrics and Gynecology, Columbia University Medical Center, 622 W 168th Street, New York, NY 10032-3725 USA.
J Obstet Gynaecol India. 2020 Feb;70(1):12-17. doi: 10.1007/s13224-018-1198-1. Epub 2019 Feb 11.
To derive a risk calculation algorithm suitable for use in India when screening for Down's syndrome using four first-trimester maternal serum markers either alone or with ultrasound nuchal translucency (NT).
Stored maternal serum samples (- 20 °C) from 411 singleton unaffected pregnancies were retrieved and measured for pregnancy-associated plasma protein (PAPP-A), free β-human chorionic gonadotropin (hCG), placental growth factor and α-fetoprotein. Samples were taken at 10-13 weeks' gestation. Equations were derived to express marker levels in multiples of the gestation-specific normal median, adjusted for maternal weight. Gaussian model parameters were derived and compared with six published non-Indian studies; NT parameters were derived from 27,647 women screened in India. On the basis of the maternal age distribution in 64,473 Indian women screened in 2016-2017, the model was used to predict test performance.
The model predicted a detection rate for a serum-only protocol of 80% for a 5% false-positive rate. Using a 1 in 250 at term Down's syndrome risk cut-off, the predicted detection rate was 78% and the false-positive rate was 4.1%. When NT was also included, the rates were 95% for 5% and 90% for 1.4%, respectively.
First-trimester screening using four serum markers only can be carried out in India. Performance is expected to be similar to the second-trimester Quad test and will also facilitate early screening for preeclampsia and open spina bifida. A protocol of NT plus the four serum markers enhances the performance compared with NT, PAPP-A and free β-hCG.
推导一种风险计算算法,适用于印度在使用四种孕早期母体血清标志物单独或联合超声颈项透明层(NT)筛查唐氏综合征时使用。
检索411例单胎未受影响妊娠的储存母体血清样本(-20°C),并检测妊娠相关血浆蛋白(PAPP-A)、游离β-人绒毛膜促性腺激素(hCG)、胎盘生长因子和甲胎蛋白。样本在妊娠10-13周时采集。推导方程以表达经母体体重校正后的妊娠特异性正常中位数倍数的标志物水平。推导高斯模型参数并与六项已发表的非印度研究进行比较;NT参数来自印度27647名接受筛查的女性。根据2016-2017年接受筛查的64473名印度女性的母体年龄分布,使用该模型预测检测性能。
该模型预测,对于仅血清检测方案,在假阳性率为5%时检测率为80%。使用足月唐氏综合征风险截断值为1/250时预测检测率为78%,假阳性率为4.1%。当同时纳入NT时,5%假阳性率时的检测率为95%;1.4%假阳性率时的检测率为90%。
在印度可以仅使用四种血清标志物进行孕早期筛查。其性能预计与孕中期四联试验相似,并且还将有助于子痫前期和开放性脊柱裂的早期筛查。与NT、PAPP-A和游离β-hCG相比,NT加四种血清标志物的方案可提高检测性能。