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“常规”遗传羊膜穿刺术的一种高灵敏度替代方法:多种尿液分析物、颈部透明带厚度和年龄。

A high-sensitivity alternative to "routine" genetic amniocentesis: multiple urinary analytes, nuchal thickness, and age.

作者信息

Bahado-Singh R, Oz U, Kovanci E, Cermik D, Copel J, Mahoney M J, Cole L

机构信息

Department of Obstetrics and Gynecology, Yale University School Of Medicine, New Haven, Connecticut 06520-8063, USA.

出版信息

Am J Obstet Gynecol. 1999 Jan;180(1 Pt 1):169-73. doi: 10.1016/s0002-9378(99)70170-5.

Abstract

OBJECTIVE

Our purpose was to evaluate the Down syndrome screening efficiency of a new algorithm consisting of multiple urinary biochemical and ultrasound markers for use in high-risk groups such as women of advanced maternal age.

STUDY DESIGN

The urinary beta-core fragment of human chorionic gonadotropin (beta-core fragment) and total urinary estriol, along with fetal nuchal thickness, were measured prospectively in pregnant women who were undergoing genetic amniocentesis at midtrimester (15 to 24 weeks). The most common indication for amniocentesis was advanced maternal age (90.2%). An analyte ratio (beta-core fragment/total estriol ratio) was developed. The values were expressed as multiples of the normal median. An increase in the observed nuchal thickness (delta nuchal thickness) above that expected on the basis of the biparietal diameter was calculated. On the basis of the mean and standard deviations of the urinary analyte ratio in normal fetuses and also Down syndrome, we calculated individual Down syndrome likelihood ratios for each of the two parameters, using gaussian analysis. The product of the likelihood ratios, based on delta nuchal thickness and urinary beta-core fragment-total estriol values times the maternal age-related risk, gave the overall Down syndrome risk. The screening efficiency of our algorithm at various risk thresholds was determined.

RESULTS

There were 13 (2.8%) cases of Down syndrome in a total study population of 457. At a risk threshold of >1 in 70, the sensitivity was 92.3% for a false-positive rate of 4.5%. Corresponding values at a risk threshold of >1 in 78 were a sensitivity of 100% with a false-positive rate of 5.2%.

CONCLUSION

By combining urinary analyte, nuchal thickness, and maternal age data, we achieved a high Down syndrome detection rate with a low false-positive rate. This algorithm would be attractive as an alternative to "routine" amniocentesis based solely on advanced maternal age. The potential benefits of this protocol could include a significant reduction in the rate of amniocentesis, along with substantial savings in medical expenditures.

摘要

目的

我们的目的是评估一种由多种尿生化和超声标志物组成的新算法对高龄产妇等高风险人群的唐氏综合征筛查效率。

研究设计

前瞻性地测量了孕中期(15至24周)接受遗传羊膜穿刺术的孕妇尿中人绒毛膜促性腺激素的β核心片段(β核心片段)和总尿雌三醇,以及胎儿颈部透明带厚度。羊膜穿刺术最常见的指征是高龄产妇(90.2%)。制定了一个分析物比值(β核心片段/总雌三醇比值)。这些值以正常中位数的倍数表示。计算观察到的颈部透明带厚度(Δ颈部透明带厚度)高于基于双顶径预期值的增加量。根据正常胎儿和唐氏综合征胎儿尿分析物比值的均值和标准差,使用高斯分析计算两个参数各自的个体唐氏综合征似然比。基于Δ颈部透明带厚度和尿β核心片段 - 总雌三醇值的似然比乘积乘以与产妇年龄相关的风险,得出总体唐氏综合征风险。确定了我们的算法在不同风险阈值下的筛查效率。

结果

在457名研究对象中,有13例(2.8%)唐氏综合征病例。在风险阈值>1/70时,敏感性为92.3%,假阳性率为4.5%。在风险阈值>1/78时,相应的值为敏感性100%,假阳性率为5.2%。

结论

通过结合尿分析物、颈部透明带厚度和产妇年龄数据,我们实现了高唐氏综合征检出率和低假阳性率。作为仅基于高龄产妇的“常规”羊膜穿刺术的替代方法,该算法将具有吸引力。该方案的潜在益处可能包括显著降低羊膜穿刺术的发生率,以及大幅节省医疗费用。

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