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妊娠中期染色体非整倍体的生化与超声筛查

[Biochemical and ultrasonic screening of chromosomal aneuploidies in the second trimester of pregnancy].

作者信息

Török O, Veress L, Szabó M, Zsupán I, Buczkó Z, Bolodár A, Harsányi A, Tóth Z

机构信息

Debreceni Orvostudományi Egyetem Szülészeti és Nögyógyászati Klinika.

出版信息

Orv Hetil. 1997 Jan 19;138(3):123-7.

PMID:9064624
Abstract

For prenatal screening of chromosomal aneuploidies (primarily the most frequent Down syndrome) maternal serum AFP screening in the second trimester of pregnancy has been supplemented by the determination of hCG in Hajdú-Bihar county. In pregnancies at risk on the basis of biochemical tests, a thorough, aimed ultrasound examination for the detection of minor and major anomalies characteristic for chromosomal abnormalities was carried out. If both biochemical and ultrasound examinations were suggestive of high risk prenatal karyotyping was offered. During a two-years prospective study 14328 pregnancies were screened. Authors could detect 38% of Down-syndrome cases prenatally, 5 cases in pregnant women at age under 35 years and at the same time the number of amniocenteses increased only by 70. It was concluded that 66% of all Down syndrome cases could have been prenatally diagnosed if prenatal chromosome test were performed in all cases at high risk on the basis of screening tests and maternal age.

摘要

在豪伊杜-比豪尔县,为进行染色体非整倍体(主要是最常见的唐氏综合征)的产前筛查,在妊娠中期的母体血清甲胎蛋白筛查中增加了人绒毛膜促性腺激素的测定。对于基于生化检测存在风险的妊娠,进行了全面、有针对性的超声检查,以检测染色体异常所特有的微小和重大异常。如果生化检查和超声检查均提示高风险,则提供产前核型分析。在一项为期两年的前瞻性研究中,对14328例妊娠进行了筛查。作者能够在产前检测出38%的唐氏综合征病例,其中5例为35岁以下孕妇,同时羊膜穿刺术的数量仅增加了70例。得出的结论是,如果根据筛查试验和孕妇年龄对所有高风险病例进行产前染色体检测,那么所有唐氏综合征病例中有66%本可在产前得到诊断。

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