Kellner L H, Weiner Z, Weiss R R, Neuer M, Martin G M, Mueenuddin M, Bombard A
Department of Pathology, Winthrop-University Hospital, State University of New York, Stony Brook School of Medicine, Mineola, USA.
Am J Obstet Gynecol. 1995 Oct;173(4):1306-9. doi: 10.1016/0002-9378(95)91376-9.
Our purpose was to compare the efficacy of triple-marker screening (alpha-fetoprotein, unconjugated estriol, human chorionic gonadotropin) with alpha-fetoprotein plus free beta-human chorionic gonadotropin.
Free beta-human chorionic gonadotropin was concurrently assayed in 2349 maternal serum samples. Trivariate and bivariate algorithms were used to calculate the risk for fetal Down syndrome by the two protocols. Free beta-human chorionic gonadotropin from 12 cases of fetal Down syndrome previously screened with the triple marker was retrospectively assayed.
Mean maternal age of our study was 29.8 years (range 14 to 51 years). The initial screen-positive rate with the triple marker was 8.0% compared with 12.8% for alpha-fetoprotein plus free beta-human chorionic gonadotropin. All three cases of fetal Down syndrome ascertained in our prospective study were detected by the triple marker; in contrast, one of three was detected by alpha-fetoprotein plus free beta-human chorionic gonadotropin. By adding 12 additional cases of fetal Down syndrome, 12 of 15 (80%) were screen positive with triple marker and nine of 15 (60%) were screen positive with alpha-fetoprotein plus free beta-human chorionic gonadotropin.
The detection rate of fetal Down syndrome was greater by use of a triple marker screen than when using alpha-fetoprotein plus free beta-human chorionic gonadotropin. Our data do not support the claims of other studies that suggest that alpha-fetoprotein plus free beta-human chorionic gonadotropin is superior to triple markers.
我们的目的是比较三联筛查(甲胎蛋白、未结合雌三醇、人绒毛膜促性腺激素)与甲胎蛋白加游离β-人绒毛膜促性腺激素的效果。
对2349份孕妇血清样本同时检测游离β-人绒毛膜促性腺激素。采用多变量和双变量算法通过两种方案计算胎儿唐氏综合征风险。对之前用三联筛查法筛查出的12例胎儿唐氏综合征病例的游离β-人绒毛膜促性腺激素进行回顾性检测。
我们研究中孕妇的平均年龄为29.8岁(范围14至51岁)。三联筛查法的初始筛查阳性率为8.0%,而甲胎蛋白加游离β-人绒毛膜促性腺激素的阳性率为12.8%。在我们的前瞻性研究中确诊的3例胎儿唐氏综合征病例均通过三联筛查法检测出;相比之下,甲胎蛋白加游离β-人绒毛膜促性腺激素仅检测出3例中的1例。增加另外12例胎儿唐氏综合征病例后,15例中有12例(80%)通过三联筛查法筛查为阳性,15例中有9例(60%)通过甲胎蛋白加游离β-人绒毛膜促性腺激素筛查为阳性。
使用三联筛查法检测胎儿唐氏综合征的检出率高于使用甲胎蛋白加游离β-人绒毛膜促性腺激素。我们的数据不支持其他研究中认为甲胎蛋白加游离β-人绒毛膜促性腺激素优于三联筛查的说法。