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无创产前检测的临床应用及随访研究
引用本文:赖允丽,陈筠,易升,周林,易赏,雷亚琴,郑海洋,林飞,邬玲仟,韦红卫.无创产前检测的临床应用及随访研究[J].重庆医学,2016(11):1491-1495.
作者姓名:赖允丽  陈筠  易升  周林  易赏  雷亚琴  郑海洋  林飞  邬玲仟  韦红卫
作者单位:1. 广西壮族自治区妇幼保健院遗传代谢中心实验室,南宁,530000;2. 山东省聊城市东昌府区妇幼保健院 252200;3. 中南大学医学遗传学国家重点实验室,长沙,410078;4. 广西壮族自治区妇幼保健院妇产科,南宁,530000
基金项目:国家科技支撑计划项目(2014BAI06B03);广西医疗卫生适宜技术研究与开发项目(S201543)。
摘    要:目的:采用大规模平行测序检测胎儿染色体疾病,通过全面随访,为无创产前检测(NIPT )的临床应用提供有效的数据支持及遗传咨询方案。方法唐氏筛查高风险的孕妇接受 NIPT ,结果提示高危者进行核型确诊,低危者进行生育前后随访。结果(1)NIPT提示胎儿异常25例,异常率为1.49%,核型确诊异常12例,均已引产,NIPT 对 T21、T18、XO、XXY、XYY的准确性依次为99.93%、100.00%、99.66%、100.00%、100.00%;在高龄妊娠和双胎妊娠中对 T 21/T 18的准确性达100.00%;产前阳性干预率达100.00%。(2)NIPT提示低风险1651例,完成随访1468例,成功率为88.91%,发现1例9号染色体倒位(母源性)。(3)B超检测染色体异常准确率达98.17%,检出率仅7.69%;唐氏筛查高风险人群的准确率仅为0.88%,假阳性率高达99.12%;NIPT避免了98.71%的孕妇进行介入性产前诊断。结论 NIPT作为现有产前检测技术的重要补充,为寻找最合适的产前筛查模式提供参考。在医疗机构建立健全NIPT随访和服务系统对降低出生缺陷疾病尤为重要。

关 键 词:无创产前检测  染色体疾病  超声检测  唐氏筛查高风险  随访研究

The clinical application and follow-up study of f non-invasive prenatal testing
Lai Yunli,Chen Yun,Yi Sheng,Zhou Lin,Yi Shang,Lei Yaqin,Zheng Haiyang,Lin Fei,Wu Lingqian,Wei Hongwei.The clinical application and follow-up study of f non-invasive prenatal testing[J].Chongqing Medical Journal,2016(11):1491-1495.
Authors:Lai Yunli  Chen Yun  Yi Sheng  Zhou Lin  Yi Shang  Lei Yaqin  Zheng Haiyang  Lin Fei  Wu Lingqian  Wei Hongwei
Abstract:Objective To provide valid data and useful genetic counseling in the clinical application of non‐invasive prenatal test (NIPT) ,fetal chromosomal disorder were screened by massive parallel sequencing and made a follow‐up study .Methods Preg‐nant women with Down screening in high‐risk were screened by NIPT ;NIPT verified high‐risk individuals were suggested for kary‐otyping ;and we follow up on whoever showed low risk by NIPT before and after their deliveries .Results (1)Totally 1 676 cases of pregnant women were tested by NIPT ,25 cases prompted to be abnormal ,with an abnormal rate of 1 .49% ,karyotype analysis re‐sults in 12 cases of abnormalit ,the accuracies of NIPT for T21 ,T18 ,XO ,XXY ,and XYY were 99 .93% ,100 .00% ,99 .66% , 100 .00% ,100 .00% respectively ;the accuracy of NIPT for women with advanced paternal age and twins were both 100 .00% ;kary‐otyping positive individuals underwent abortion ,which gives a prenatal intervention rate of 100 .00% .(2)Out of 1 651 cases of NIPT low risk testers ,1 468 cases were successfully followed up ,with a 88 .91% success rate .We found chromosome abnormality with one case of inversion of chromosome 9 (maternal) .(3)Ultrasound‐detection possessed 98 .17% accuracy and 7 .69% in detec‐tion rate;in high‐risk pregnant woman ,Down screening had an accuracy of 0 .88% and false positive rate of 99 .12% ;98 .71%women were avoided prenatal diagnosis via NIPT .Conclusion Compare to ultrasound and maternal plasma screening ,NIPT is a far more accurate prenatal screening approach .To build effective follow‐up and service systems of NIPT is necessary to reduce birth de‐fects in medical institutions .
Keywords:non-invasive prenatal test  chromosomal abnormality  ultrasonic test  Down screening in high-risk  follow-up study
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