Ye Qiang, Huang Guoping, Hu Qin, Man Qin, Hao Xiaoying, Liu Liangyan, Zhong Qiang, Jin Zhao
Department of Clinical Laboratory, West China Second University Hospital, Southern Sichuan Women's and Children's Hospital, Zigong, Sichuan, 643000, People's Republic of China.
Department of Prenatal Diagnosis Center, West China Second University Hospital, Southern Sichuan Women's and Children's Hospital, Zigong, Sichuan, 643000, People's Republic of China.
Int J Womens Health. 2024 Mar 29;16:563-573. doi: 10.2147/IJWH.S455778. eCollection 2024.
This study was to evaluate the performance of noninvasive prenatal testing (NIPT) in detecting fetal chromosome disorders in pregnant women.
From October 1st, 2017, to December 31th, 2022, a total of 15,304 plasma cell free DNA-NIPT samples were collected for fetal chromosome disorders screening. The results of NIPT were validated by confirmatory invasive testing or clinical outcome follow-up. Further, NIPT performance between low-risk and high-risk groups, as well as singleton pregnancy and twin pregnancy groups was compared. Besides, analysis of 111 false-positive cases was performed.
Totally, NIPT was performed on 15,086 eligible venous blood samples, of which 179 (1.19%) showed positive NIPT results and 68 were further validated to be true positive samples via confirmatory invasive testing or follow-up of clinical outcomes. For common chromosome aneuploidies, sex chromosome abnormalities (SCA) and other chromosomal aneuploidies, the detection sensitivities of NIPT were all 100%, the specificities were 99.87%, 99.70%, and 99.68% and the positive predictive values (PPVs) were 65.45%, 31.82%, and 10.91%, respectively. No statistically significant variance in detection performance was observed among 2987 high-risk and 12,099 low-risk subjects, as well as singleton and twin pregnancy subjects. The concentration of cell-free fetal DNA of 111 false-positive cases ranged from 5.5% to 33.7%, which was higher than the minimum requirement of NIPT.
With stringent protocol, NIPT shows high sensitivity and specificity for detecting fetal chromosome disorders in a large-scale clinical service, helping improving overall pregnancy management.
本研究旨在评估无创产前检测(NIPT)在检测孕妇胎儿染色体疾病中的性能。
2017年10月1日至2022年12月31日,共收集15304份血浆游离DNA-NIPT样本用于胎儿染色体疾病筛查。NIPT结果通过侵入性确诊检测或临床结局随访进行验证。此外,比较了低风险组和高风险组以及单胎妊娠组和双胎妊娠组之间的NIPT性能。此外,对111例假阳性病例进行了分析。
总共对15086份合格静脉血样本进行了NIPT检测,其中179份(1.19%)NIPT结果呈阳性,68份通过侵入性确诊检测或临床结局随访进一步验证为真阳性样本。对于常见染色体非整倍体、性染色体异常(SCA)和其他染色体非整倍体,NIPT的检测灵敏度均为100%,特异性分别为99.87%、99.70%和99.68%,阳性预测值(PPV)分别为65.45%、31.82%和10.91%。在2987名高风险和12099名低风险受试者以及单胎和双胎妊娠受试者中,未观察到检测性能的统计学显著差异。111例假阳性病例的游离胎儿DNA浓度范围为5.5%至33.7%,高于NIPT的最低要求。
通过严格的方案,NIPT在大规模临床服务中对检测胎儿染色体疾病显示出高灵敏度和特异性,有助于改善整体妊娠管理。