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产前母体干血筛查甲胎蛋白和游离β-人绒毛膜促性腺激素以检测开放性神经管缺陷和唐氏综合征。

Prenatal maternal dried blood screening with alpha-fetoprotein and free beta-human chorionic gonadotropin for open neural tube defect and Down syndrome.

作者信息

Macri J N, Anderson R W, Krantz D A, Larsen J W, Buchanan P D

机构信息

Research Division, NTD Laboratories, Inc., Huntington Station, NY 11746, USA.

出版信息

Am J Obstet Gynecol. 1996 Feb;174(2):566-72. doi: 10.1016/s0002-9378(96)70429-5.

Abstract

OBJECTIVE

Our purpose was to evaluate second-trimester prenatal screening for open neural tube defects and Down syndrome by use of dried blood specimen collection and transport.

STUDY DESIGN

A prospective study of 7497 dried blood specimens from patients <35 years old was performed. Specimens were assayed for maternal blood alpha-fetoprotein and free beta-human chorionic gonadotropin. Patient-specific risks for both disorders were calculated and used to determine whether further evaluation was indicated. The study included an evaluation of the median and SD of analyte multiple of the median levels.

RESULTS

The initial positive rate for open neural tube defect was 4.4% adjusted to 2.7% after ultrasonographic revision and collection of a second sample. The initial positive rate for Down syndrome was 3.6% adjusted to 2.8% after ultrasonographic revision. All seven cases of open neural tube defect were detected within the increased risk group. Six of 8 (75%) cases of Down syndrome were detected. The median alpha-fetoprotein multiple of the median was 3.5 in open neural tube defect cases and 0.6 in Down syndrome cases. The median free beta-human chorionic gonadotropin multiple of the median was 2.4 in Down syndrome cases. The SD (log e) of alpha- fetoprotein and free beta-human chorionic gonadotropin in 5868 unaffected white patients was 0.4022 and 0.5635, respectively.

CONCLUSION

Second-trimester dried blood screening for open neural tube defects and Down syndrome can achieve screening efficiency comparable to serum-based protocols with distinct advantages over the conventional method of blood collection.

摘要

目的

我们的目的是评估利用干血标本采集和运输进行孕中期开放性神经管缺陷和唐氏综合征的产前筛查。

研究设计

对7497例年龄小于35岁患者的干血标本进行了一项前瞻性研究。对标本进行母体血甲胎蛋白和游离β-人绒毛膜促性腺激素检测。计算这两种疾病的患者特异性风险,并用于确定是否需要进一步评估。该研究包括对分析物中位数倍数水平的中位数和标准差的评估。

结果

开放性神经管缺陷的初始阳性率为4.4%,经超声检查修正并采集第二份样本后调整为2.7%。唐氏综合征的初始阳性率为3.6%,经超声检查修正后调整为2.8%。所有7例开放性神经管缺陷病例均在风险增加组中被检测到。8例唐氏综合征病例中有6例(75%)被检测到。开放性神经管缺陷病例中甲胎蛋白中位数倍数的中位数为3.5,唐氏综合征病例中为0.6。唐氏综合征病例中游离β-人绒毛膜促性腺激素中位数倍数的中位数为2.4。5868例未受影响的白人患者中甲胎蛋白和游离β-人绒毛膜促性腺激素的标准差(自然对数)分别为0.4022和0.5635。

结论

孕中期干血筛查开放性神经管缺陷和唐氏综合征可实现与基于血清的方案相当的筛查效率,且相对于传统采血方法具有明显优势。

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