Mooney R A, Peterson C J, French C A, Saller D N, Arvan D A
Department of Pathology, University of Rochester Medical Center, New York.
Obstet Gynecol. 1994 Aug;84(2):298-303.
To evaluate the efficacy of combining hCG and alpha-fetoprotein (AFP) with maternal age in a two-analyte maternal serum screening program for Down syndrome.
A prospective study involved the screening of 12,170 maternal sera from patients at 14-25 weeks of gestation. The risk for Down syndrome at term was calculated from maternal serum hCG and AFP, and maternal age. For women 36 years of age and younger, a risk of 1:307 or greater was considered screen-positive. For women over 36, a risk greater than that a priori was considered screen-positive. False-positive rates and detection rates were compared with those resulting from a screening protocol using only AFP and age.
Seven hundred eighty-two sera were initially screen-positive (6.4%). Subsequent sonography decreased this total to 687 (5.6%), and 467 (3.8%) of these patients accepted amniocentesis. Ten cases of Down syndrome and seven other chromosomal abnormalities were detected. Follow-up investigations revealed eight additional Down syndrome cases that were missed by screening. The identification of 18 Down syndrome cases in 12,170 pregnancies corresponds closely with the prediction of 14.1 Down syndrome births (18.2 second-trimester fetuses) in this population calculated from age-dependent risks. The detection rate for Down syndrome was 56% (ten of 18 expected cases). Only five of 18 (28%) would have been detected by AFP and age alone.
These results support the mathematical model that hCG is the major contributor to the increased sensitivity of multi-analyte screening and demonstrate that screening programs can attain substantial improvement in detection of second-trimester Down syndrome by adding hCG to AFP and age.
评估在一项用于唐氏综合征的双分析物孕妇血清筛查项目中,将人绒毛膜促性腺激素(hCG)和甲胎蛋白(AFP)与孕妇年龄相结合的效果。
一项前瞻性研究纳入了12170例妊娠14 - 25周孕妇的血清筛查。根据孕妇血清hCG、AFP及孕妇年龄计算足月时患唐氏综合征的风险。对于36岁及以下的女性,风险为1:307或更高被视为筛查阳性。对于36岁以上的女性,风险高于先验风险被视为筛查阳性。将假阳性率和检出率与仅使用AFP和年龄的筛查方案所得到的结果进行比较。
最初有782份血清筛查呈阳性(6.4%)。随后的超声检查使这一总数降至687份(5.6%),其中467例(3.8%)患者接受了羊膜穿刺术。检测到10例唐氏综合征和7例其他染色体异常。后续调查发现另外8例唐氏综合征病例筛查漏诊。在12170例妊娠中识别出18例唐氏综合征病例,这与根据年龄相关风险计算出的该人群中14.1例唐氏综合征出生(18.2例孕中期胎儿)的预测结果密切相符。唐氏综合征的检出率为56%(18例预期病例中的10例)。仅靠AFP和年龄,18例中只能检测出5例(28%)。
这些结果支持了hCG是多分析物筛查敏感性提高的主要贡献因素的数学模型,并表明通过在AFP和年龄基础上增加hCG,筛查项目在孕中期唐氏综合征检测方面可实现显著改善。