Application of non-invasive prenatal genetic testing in prenatal anomaly index screening
10.3760/cma.j.issn.1009-9158.2018.07.006
- VernacularTitle: 无创产前基因检测在产前筛查异常指标中的应用
- Author:
Fangfang GUO
1
;
Jiexia YANG
;
Yiming QI
;
Yaping HOU
;
Haishan PENG
;
Dongmei WANG
;
Haoxin OUYANG
;
Aihua YIN
Author Information
1. Prenatal Diagnosis Centre, Guangdong Women and Children Hospital, Guangzhou 510010, China
- Publication Type:Journal Article
- Keywords:
Aneuploidy;
Prenatal diagnosis;
Genetic testing;
Nuchal translucency measurement
- From:
Chinese Journal of Laboratory Medicine
2018;41(7):509-513
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To evaluate the value of non-invasive prenatal testing (NIPT) in pregnancies with anomaly in prenatal screening.
Methods:This was a retrospective study of 2 837 singleton pregnancies who performed NIPT indicated by isolated anomaly in prenatal screening at Guangdong Women and Children Hospital between November 2014 and August 2016. All pregnancies were divided into 3 groups by single indication: advanced maternal age ( AMA, ≥35), abnormal multiples of the median (MoM) in standard screening, increased nuchal translucency thickness (NT, 2.5-3.0 mm). High risk results were verified by prenatal diagnosis. Low risk cases were followed by a 22-26 week anatomical ultrasound examination. All of the cases were followed up and the performance of NIPT for every single indication was evaluated.
Results:There were total of 2 837 pregnant women who underwent NIPT. Twenty-five of 2 448 pregnancies indicated by AMA had high risk results, among which 17 were confirmed by invasive genetic testing, except 1 case rejecting prenatal diagnosis. In 351 pregnant women with abnormal MoM, NIPT found 3 cases of sex chromosome aneuploidies (SCA) and 2 of them were validated by invasive prenatal diagnosis. Increased NT group included 38 cases, NIPT found 1 case of trisomy 21 which was consistent with karyotype analysis. For common aneuploidies and SCA, the performance of NIPT in the pregnant women who indicated by AMA, abnormal MoM and increased NT were as the follows: the sensitivity were 17/17, 2/2 and 1/1 respectively, the specificity were 99.7% (2 423/2 431), 99.7% (348/349) and 100%(37/37), the positive predictive value were 68% (17/25), 2/3 and 1/1, the negative predictive value were 100% (2 423/2 423), 100% (348/348) and 100% (38/38), respectively. By follow-up survey, a total of 8 cases of abnormal fetus were recorded in NIPT low-risk women, including 5 cases of termination of pregnancy due to abnormal ultrasound findings, 2 cases of abortion as a result of severe obstetric complications and 1 case of stillbirth.
Conclusions:To the pregnant women who indicated by advanced maternal age, abnormal MoM and increased NT (2.5-3.0 mm), NIPT had satisfactory performance for common aneuploidies, and also had potential value for SCA, resulting in a significant reduction in diagnostic procedures. However, for NIPT low-risk pregnancies, routine antenatal examination and anatomical ultrasound detection would be highly necessary to avoid missing abnormal fetuses.(Chin J Lab Med, 2018, 41: 509-513)
