Non-invasive prenatal testing for the detection of trisomies 21, 18, and 13 in pregnant women with various clinical indications: A multicenter observational study of 1,854,148 women in China

被引:12
作者
Xiang, Liangcheng [1 ]
Zhu, Jun [2 ,3 ]
Deng, Kui [1 ]
Li, Qi [1 ]
Tao, Jing [1 ]
Li, Mingrong [1 ]
Wang, Yanping [2 ]
Yuan, Xuelian [1 ]
Yao, Yongna [2 ]
Li, Xiaohong [3 ,4 ,5 ]
机构
[1] Sichuan Univ, West China Second Univ Hosp, Natl Off Maternal & Child Hlth Surveillance China, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Second Univ Hosp, Natl Ctr Birth Defect Monitoring China, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, Key Lab Birth Defects & Related Dis Women & Childr, Minist Educ, Chengdu, Sichuan, Peoples R China
[4] Sichuan Univ, West China Second Univ Hosp, Sichuan Birth Defects Clin Res Ctr, Chengdu, Sichuan, Peoples R China
[5] Sichuan Univ, Key Lab Birth Defects & Related Dis Women & Childr, Minist Educ, 17,Sect 3, Ren Min South Rd, Chengdu 610041, Sichuan, Peoples R China
关键词
CELL-FREE DNA; FREE FETAL DNA; POSITION STATEMENT; ANEUPLOIDY; MOSAICISM; ACCURACY;
D O I
10.1002/pd.6312
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ObjectiveThis study aimed to evaluate the performance of noninvasive prenatal testing (NIPT) for detecting three common trisomies (T21, T18, and T13) in pregnant women with diverse clinical indications. MethodsFrequencies of NIPT, of high chance of having one of the three trisomies, and of confirmed trisomies were determined for women with each of seven clinical indications in a national cross-sectional survey of approximately 300 prenatal diagnosis centers. Data were collected for the period from October 1, 2016 to September 30, 2018 using the Prenatal Diagnosis Technology Management On-line Information System. The performance of NIPT for detecting the three trisomies in pregnant women with different clinical indications was assessed in terms of sensitivity, specificity, positive predictive value (PPV), negative predictive value, and the corresponding 95% confidence intervals. ResultsA total of 5766 true positive cases for T21, T18, and T13 were detected among 1,854,148 samples, giving an overall detection rate of 0.31% (95% CI: 0.30%-0.32%). Most positive cases were associated with "NT thickening" (1.18%) and "advanced maternal age" (0.51%). The detection sensitivities of NIPT were 99.60% for T21, 99.14% for T18, and 100% for T13, while the corresponding specificities were 99.90%, 99.94%, and 99.95%. The corresponding PPVs were 69.77%, 47.24%, and 22.36%. NIPT showed high sensitivity and specificity, regardless of clinical indication. In contrast, PPV for three trisomies varied widely between 9.09% and 66.46% depending on the clinical indication. Across seven clinical indications, PPV ranged from 50.62% to 73.09% for T21, 20.00%-58.33% for T18, and 4.17%-47.37% for T13. The highest PPVs were 73.09% for T21 in pregnancies involving "advanced maternal age", 58.33% for T18 in pregnancies with "NT thickening", and 47.37% for T13 in pregnancies with "NT thickening". ConclusionsNIPT shows high sensitivity and specificity for detecting T21, T18, and T13 in pregnant women with different clinical indications. However, PPV depends strongly on clinical indication, highlighting the need to strengthen education and genetic counseling about prenatal screening.
引用
收藏
页码:1036 / 1043
页数:8
相关论文
共 31 条
[11]   Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics [J].
Gregg, Anthony R. ;
Skotko, Brian G. ;
Benkendorf, Judith L. ;
Monaghan, Kristin G. ;
Bajaj, Komal ;
Best, Robert G. ;
Klugman, Susan ;
Watson, Michael S. .
GENETICS IN MEDICINE, 2016, 18 (10) :1056-1065
[12]   High throughput non-invasive determination of foetal Rhesus D status using automated extraction of cell-free foetal DNA in maternal plasma and mass spectrometry [J].
Grill, Simon ;
Banzola, Irina ;
Li, Ying ;
Rekhviashvili, Tea ;
Legler, Tobias J. ;
Mueller, Sina P. ;
Zhong, Xiao Yan ;
Hahn, Sinuhe ;
Holzgreve, Wolfgang .
ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2009, 279 (04) :533-537
[13]   Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing [J].
Liang, Desheng ;
Lv, Weigang ;
Wang, Hua ;
Xu, Liangpu ;
Liu, Jing ;
Li, Haoxian ;
Hu, Liang ;
Peng, Ying ;
Wu, Lingqian .
PRENATAL DIAGNOSIS, 2013, 33 (05) :409-415
[14]   Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China [J].
Liu, Yanhui ;
Liu, Hailiang ;
He, Yi ;
Xu, Wanfang ;
Ma, Qiulin ;
He, Yuzhen ;
Lei, Wei ;
Chen, Guoquan ;
He, Zheng ;
Huang, Jiayi ;
Liu, Jianan ;
Liu, Yuanru ;
Huang, Quanfei ;
Yu, Fubing .
HUMAN GENOMICS, 2020, 14 (01)
[15]   The accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis [J].
Mackie, F. L. ;
Hemming, K. ;
Allen, S. ;
Morris, R. K. ;
Kilby, M. D. .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2017, 124 (01) :32-46
[16]   Is it time to sound an alarm about false-positive cell-free DNA testing for fetal aneuploidy? [J].
Mennuti, Michael T. ;
Cherry, Athena M. ;
Morrissette, Jennifer J. D. ;
Dugoff, Lorraine .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2013, 209 (05) :415-419
[17]   Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 [J].
Mersy, E. ;
Smits, L. J. M. ;
van Winden, L. A. A. P. ;
de Die-Smulders, C. E. M. ;
Paulussen, A. D. C. ;
Macville, M. V. E. ;
Coumans, A. B. C. ;
Frints, S. G. M. .
HUMAN REPRODUCTION UPDATE, 2013, 19 (04) :318-329
[18]  
National Health Commission of the People's Republic of China, STAT B CHIN HLTH DEV
[19]  
National health commission of the people's republic of china, TECHNICAL SPECIFICAT
[20]   Cell-free DNA Analysis for Noninvasive Examination of Trisomy [J].
Norton, Mary E. ;
Jacobsson, Bo ;
Swamy, Geeta K. ;
Laurent, Louise C. ;
Ranzini, Angela C. ;
Brar, Herb ;
Tomlinson, Mark W. ;
Pereira, Leonardo ;
Spitz, Jean L. ;
Hollemon, Desiree ;
Cuckle, Howard ;
Musci, Thomas J. ;
Wapner, Ronald J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (17) :1589-1597