Analysis of the results of chromosomal trisomies 21, 18 and 13 screening among 40 628 women by non-invasive prenatal testing.
10.3760/cma.j.cn511374-20200819-00610
- Author:
Dongmei WANG
1
;
Jiexia YANG
;
Haishan PENG
;
Yaping HOU
;
Yixia WANG
Author Information
1. Medical Genetics Centre, Maternal and Child Health Care Hospital of Guangdong Province, Guangzhou, Guangdong 511442, China. 894606490@qq.com.
- Publication Type:Journal Article
- MeSH:
Aneuploidy;
Chromosome Disorders/genetics*;
Chromosomes;
DNA Copy Number Variations;
Down Syndrome/genetics*;
Female;
Humans;
Pregnancy;
Prenatal Diagnosis;
Trisomy/genetics*;
Trisomy 18 Syndrome/genetics*
- From:
Chinese Journal of Medical Genetics
2021;38(11):1045-1050
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To assess the clinical value of non-invasive prenatal testing (NIPT) for the screening of trisomy and copy number variations (CNVs) of chromosomes 21, 18 and 13.
METHODS:From January 2015 to December 2019, 40 628 pregnant women underwent NIPT testing using high-throughput sequencing and bioinformatics analysis to test the cell-free fetal DNA in maternal plasma. High-risk pregnant women underwent invasive prenatal diagnosis, while low-risk ones were followed up by telephone.
RESULTS:The three most common indications included intermediate risk of serological screening, high risk of serological screening and advanced maternal age. Among all pregnant women, 257 cases were detected as trisomy 21, 18 and 13 (170, 49 and 38 cases, respectively). 227 cases chose invasive prenatal diagnosis, with respectively 122, 28 and 10 cases confirmed. The positive predictive value (PPV) was 81.33% (122/150), 65.12% (28/43), 29.41% (10/34), respectively. Two false negative cases of trisomy 18 were found during follow-up. Meanwhile, NIPT has detected 46 cases (15, 16 and 15 cases, respectively) CNVs on chromosomes 21, 18 and 13, among which 37 cases underwent invasive prenatal diagnosis. There were 5, 3 and 5 positive cases, which yielded a PPV of 41.67% (5/12), 25%(3/12) and 33.33%(5/15), respectively. Two other chromosome CNVs were accidentally discovered among the false positive samples.
CONCLUSION:The incidence of chromosomal abnormalities in the serological screening high-risk group was 52.02%, which was significantly higher than other groups. NIPT has a high sensitivity and specificity for the screening of trisomies 21, 18 and 13, while its accuracy for detecting CNVs of chromosomes 21, 18 and 13 needs to be improved. As a screening method, NIPT has a great clinical value, though there are still limitations of false positive and false negative results.Comprehensive pre- and post-test genetic counseling should be provided to the patients.
