David M, Merksamer R, Israel N, Dar H
Simon Winter Institute of Human Genetics, Bnai Zion Medical Center, Technion, Haifa, Israel.
Fetal Diagn Ther. 1996 Mar-Apr;11(2):99-105. doi: 10.1159/000264287.
The effectiveness of unconjugated estriol (uE3) as a serum marker for the detection of Down syndrome (DS) during the 2nd trimester of pregnancy was evaluated. A population of 18,764 normal singleton pregnancies was screened for alpha-feto-protein and human chorionic gonadotropin. In 9,311 women, uE3 was added. Using a risk of 1:250 at term as a cutoff value, the false-positive rates were 4.1 and 4.3% without and with uE3, respectively. The detection rates in 47 DS serum samples, some of which were studied retrospectively, were 66% without uE3 and 57% with uE3. In 12 of 25 younger women and in 19 of 22 older women, DS was detected without uE3. The uE3 contributed to the detection of 4 additional DS pregnancies (1 in the young and 3 in older women). On the other hand, 8 DS pregnancies (3 in younger women and 5 in older women) escaped detection. In our sample the addition of uE3 lowered the detection rate of DS pregnancies with only a small and insignificant effect on the false-positive rate. Our results call for special caution in the addition of markers for risk calculations. We suggest that pregnancies with a calculated risk of > 1:250 following maternal serum alpha-fetoprotein and human chorionic gonadotropin markers tests should be regarded as high-risk pregnancies, even in cases in whom the addition of uE3 lowers the risk beneath the cutoff value.
评估了未结合雌三醇(uE3)作为妊娠中期检测唐氏综合征(DS)血清标志物的有效性。对18764例正常单胎妊娠人群进行了甲胎蛋白和人绒毛膜促性腺激素筛查。在9311名女性中加入了uE3检测。以足月时1:250的风险作为临界值,未加uE3和加uE3时的假阳性率分别为4.1%和4.3%。对47份DS血清样本(其中部分为回顾性研究)的检测率,未加uE3时为66%,加uE3时为57%。在25名年轻女性中的12名以及22名年长女性中的19名中,未加uE3时检测出了DS。uE3又额外检测出4例DS妊娠(年轻女性中1例,年长女性中3例)。另一方面,有8例DS妊娠(年轻女性中3例,年长女性中5例)未被检测出。在我们的样本中,加入uE3降低了DS妊娠的检测率,而对假阳性率只有微小且不显著的影响。我们的结果提醒在添加用于风险计算的标志物时要格外谨慎。我们建议,在进行母血清甲胎蛋白和人绒毛膜促性腺激素标志物检测后,计算出风险>1:250的妊娠应被视为高危妊娠,即使在加入uE3后风险降至临界值以下的情况下。