Suppr超能文献

印度北部一家政府医院的二孕期母血清学筛查用于染色体异常和神经管缺陷。

Maternal serum second trimester screening for chromosomal disorders and neural tube defects in a government hospital of North India.

机构信息

Genetic Centre, Government Medical College and Hospital, Chandigarh, India.

出版信息

Prenat Diagn. 2012 Dec;32(12):1192-6. doi: 10.1002/pd.3984. Epub 2012 Oct 11.

Abstract

OBJECTIVE

Down syndrome (DS) has major resource implications especially in developing countries being third most important cause of mental handicap. Maternal serum screening for chromosomal aneuploidies and neural tube defects (NTDs) is practiced worldwide in many countries and has been integrated into mainstream health care, while it is gradually gaining momentum in Asian countries.

METHODS

This prospective cohort study was carried out in pregnant women undergoing triple screening test between January 2007 and December 2010 after informed consent. Biomarkers alpha-fetoprotein, human-chorionic-gonadotropin and unconjugated-estriol were tested, and risk of pregnancy being affected with DS, Edward's syndrome or NTDs were calculated. Screen-positive patients were referred for detailed ultrasonography and confirmatory amniocentesis. Follow-up record was maintained until delivery.

RESULTS

Of 7400 pregnant women enrolled, 419(5.7%) were screen-positive, including 339 positive for DS, two for trisomy 18, and 62 for NTDs. Total eight cases of DS were eventually diagnosed in the population (prevalence of DS = 1 : 925), seven of which were detected in utero following diagnostic evaluation for positive serum screen (DR of DS screen = 87.5%). Total five cases of NTD were observed, yielding NTD prevalence of 0.67/1000.

CONCLUSIONS

Triple screening in the second trimester is reasonably effective for the detection of major chromosomal defects and NTDs, and can be implemented successfully also in India.

摘要

目的

唐氏综合征(DS)在发展中国家是导致精神障碍的第三大重要原因,因此需要大量资源,尤其是在发展中国家。全世界许多国家都在进行母血清筛查以检测染色体非整倍体和神经管缺陷(NTD),并将其纳入主流医疗保健,而在亚洲国家也在逐渐普及。

方法

本前瞻性队列研究于 2007 年 1 月至 2010 年 12 月在知情同意后进行,对接受三联筛查试验的孕妇进行研究。检测了甲胎蛋白、人绒毛膜促性腺激素和未结合雌三醇等生物标志物,并计算了妊娠患 DS、爱德华氏综合征或 NTD 的风险。对筛查阳性的患者进行详细的超声检查和确诊性羊膜穿刺术。进行随访记录,直至分娩。

结果

在 7400 名纳入的孕妇中,有 419 名(5.7%)筛查阳性,其中 339 名 DS 阳性,2 名 18 三体阳性,62 名 NTD 阳性。在该人群中最终诊断出 8 例 DS(发病率为 1:925),其中 7 例在进行阳性血清筛查的诊断评估后在宫内检出(DS 筛查的诊断率为 87.5%)。共观察到 5 例 NTD,NTD 的患病率为 0.67/1000。

结论

在妊娠中期进行三联筛查对于检测主要染色体缺陷和 NTD 是合理有效的,并且在印度也可以成功实施。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验