Cole L A, Shahabi S, Oz U A, Bahado-Singh R O, Mahoney M J
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, CT 06510, USA.
Clin Chem. 1999 Dec;45(12):2109-19.
Serum human chorionic gonadotropin (hCG) and hCG free beta-subunit tests are used in combination with unconjugated estriol and alpha-fetoprotein in the triple screen test, and with the addition of inhibin-A in the quadruple marker test for detecting Down syndrome in the second trimester of pregnancy. These tests have a limited detection rate for Down syndrome: approximately 40% for hCG or free beta-subunit alone, approximately 60% for the triple screen test, and approximately 70% for the quadruple marker test, all at 5%, or a relatively high, false-positive rate. New tests are needed with higher detection and lower false rates. Hyperglycosylated hCG (also known as invasive trophoblast antigen or ITA) is a new test. It specifically detects a unique oligosaccharide variant of hCG associated with Down syndrome pregnancies. We evaluated this new Down syndrome-directed test in prenatal diagnosis.
Hyperglycosylated hCG was measured in urine samples from women undergoing amniocentesis for advanced maternal age concerns at 14-22 weeks of gestation, 1448 with normal karyotype and 39 with Down syndrome fetuses.
The median hyperglycosylated hCG value was 9.5-fold higher in Down syndrome cases (9.5 multiples of the normal karyotype median). The single test detected 80% of Down syndrome cases at a 5% false-positive rate. Urine hyperglycosylated hCG was combined with urine beta-core fragment (urine breakdown product of serum hCG free beta-subunit), serum alpha-fetoprotein, and maternal age-related risk. This urine-serum combination detected 96% of Down syndrome cases at a 5% false-positive rate, 94% of cases at a 3% false-positive rate, and 71% of cases at a 1% false-positive rate. These detection rates exceed those of any previously reported combination of biochemical markers.
Hyperglycosylated hCG is a new base marker for Down syndrome screening in the second trimester of pregnancy. The measurement of hyperglycosylated hCG can fundamentally improve the performance of Down syndrome screening protocols.
血清人绒毛膜促性腺激素(hCG)和游离β亚基hCG检测与未结合雌三醇和甲胎蛋白联合用于三联筛查试验,而四联标志物检测在此基础上增加了抑制素A,用于在妊娠中期检测唐氏综合征。这些检测对唐氏综合征的检出率有限:单独检测hCG或游离β亚基时约为40%,三联筛查试验约为60%,四联标志物检测约为70%,且假阳性率均为5%,即相对较高。需要具有更高检出率和更低假阳性率的新检测方法。高糖基化hCG(也称为侵袭性滋养层抗原或ITA)就是一种新的检测方法。它能特异性检测与唐氏综合征妊娠相关的hCG独特寡糖变体。我们在产前诊断中对这种针对唐氏综合征的新检测方法进行了评估。
对因高龄产妇担忧在妊娠14 - 22周接受羊膜穿刺术的女性尿液样本进行高糖基化hCG检测,其中1448例胎儿核型正常,39例胎儿患有唐氏综合征。
唐氏综合征病例中高糖基化hCG的中位数是正常核型中位数的9.5倍。该单项检测在假阳性率为5%时能检测出80%的唐氏综合征病例。尿液高糖基化hCG与尿液β核心片段(血清游离β亚基hCG的尿液分解产物)、血清甲胎蛋白以及与产妇年龄相关的风险相结合。这种尿液 - 血清联合检测在假阳性率为5%时能检测出96%的唐氏综合征病例,在假阳性率为3%时能检测出94%的病例,在假阳性率为1%时能检测出71%的病例。这些检出率超过了此前报道的任何生化标志物组合的检出率。
高糖基化hCG是妊娠中期唐氏综合征筛查的一种新的基础标志物。高糖基化hCG的检测可从根本上提高唐氏综合征筛查方案的性能。