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对孕中期唐氏综合征和18三体血清筛查的敏感性和假阳性率的估计,并对交叉识别和双阳性结果进行了调整。

Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results.

作者信息

Benn P A, Ying J, Beazoglou T, Egan J F

机构信息

Division of Human Genetics, Department of Pediatrics, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030-6140, USA.

出版信息

Prenat Diagn. 2001 Jan;21(1):46-51.

Abstract

Second trimester screening for fetal Down syndrome and trisomy 18 is available through separate protocols that combine the maternal age-specific risk and the analysis of maternal serum markers. We have determined the extent to which additional Down syndrome affected pregnancies may be identified through trisomy 18 screening, and the extent to which additional cases of trisomy 18 may be screen-positive for Down syndrome. The combined false-positive rate, taking into consideration those pregnancies that are screen-positive by both protocols, has also been determined. Sensitivity and false-positive rates were determined by computer simulation of results that incorporated previously published statistical variables into the model. Using second trimester risk cut-offs of 1:270 for Down syndrome and 1:100 for trisomy 18, it was found that few additional cases of Down syndrome are identified through trisomy 18 screening. However, approximately 6-10% of trisomy 18 affected pregnancies will be screen-positive for Down syndrome but screen-negative for trisomy 18. For women aged 40 or more, the false-positive rate for trisomy 18 exceeds 1% and approximately half of these cases will also be screen-positive for Down syndrome. For a population with maternal ages equivalent to that in the United States in 1998, after adjusting for the cross-identification, the sensitivity for three-analyte trisomy 18 screening is 78%. If this testing is performed in conjunction with Down syndrome "triple" screening, the Down syndrome sensitivity is 75% and the combined false-positive rate is 8.5%. If the three-analyte trisomy 18 screening is performed with the Down syndrome "quad" screen, the trisomy 18 sensitivity remains at 78%, the Down syndrome sensitivity is 79%, and combined false-positive rate is 7.5%. Sensitivity and false-positive rates are also provided for other widely used Down syndrome and trisomy 18 risk cut-offs. Sensitivity and false-positive rates that take into consideration cross-identification and double-positives should be helpful for pre-test counseling and the evaluation of serum screening programs.

摘要

孕中期对胎儿唐氏综合征和18三体综合征的筛查可通过单独的方案进行,这些方案结合了特定孕龄的母亲风险以及母体血清标志物分析。我们已经确定了通过18三体综合征筛查可额外识别出唐氏综合征妊娠的程度,以及额外的18三体综合征病例在唐氏综合征筛查中呈阳性的程度。还确定了综合假阳性率,其中考虑了两种方案筛查均呈阳性的妊娠。敏感性和假阳性率通过计算机模拟结果来确定,该结果将先前发表的统计变量纳入模型。使用孕中期唐氏综合征风险截断值为1:270和18三体综合征风险截断值为1:100,发现通过18三体综合征筛查识别出的唐氏综合征额外病例很少。然而,约6 - 10%的18三体综合征妊娠在唐氏综合征筛查中呈阳性,但在18三体综合征筛查中呈阴性。对于40岁及以上的女性,18三体综合征的假阳性率超过1%,其中约一半病例在唐氏综合征筛查中也呈阳性。对于1998年美国孕龄相当的人群,在调整交叉识别后,三项分析物18三体综合征筛查的敏感性为78%。如果该检测与唐氏综合征“三联”筛查同时进行,唐氏综合征的敏感性为75%,综合假阳性率为8.5%。如果三项分析物18三体综合征筛查与唐氏综合征“四联”筛查同时进行,18三体综合征的敏感性仍为78%,唐氏综合征的敏感性为79%,综合假阳性率为7.5%。还提供了其他广泛使用的唐氏综合征和18三体综合征风险截断值的敏感性和假阳性率。考虑交叉识别和双阳性的敏感性和假阳性率应有助于检测前咨询和血清筛查项目的评估。

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