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Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China

BACKGROUND: The relatively high incidence and the clinical symptoms of sex chromosome aneuploidies (SCAs) make prenatal screening of SCAs an attractive option for pregnant women. However, limited studies have assessed the clinical performance of noninvasive prenatal testing (NIPT) for screening SCAs...

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Autores principales: Zhao, Ganye, Dai, Peng, Wang, Conghui, Liu, Lina, Zhao, Xuechao, Kong, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825788/
https://www.ncbi.nlm.nih.gov/pubmed/35155454
http://dx.doi.org/10.3389/fmed.2021.672211
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author Zhao, Ganye
Dai, Peng
Wang, Conghui
Liu, Lina
Zhao, Xuechao
Kong, Xiangdong
author_facet Zhao, Ganye
Dai, Peng
Wang, Conghui
Liu, Lina
Zhao, Xuechao
Kong, Xiangdong
author_sort Zhao, Ganye
collection PubMed
description BACKGROUND: The relatively high incidence and the clinical symptoms of sex chromosome aneuploidies (SCAs) make prenatal screening of SCAs an attractive option for pregnant women. However, limited studies have assessed the clinical performance of noninvasive prenatal testing (NIPT) for screening SCAs. This study was performed to evaluate the clinical performance of NIPT for SCAs in singleton pregnancies in central China. METHODS: Noninvasive prenatal testing was performed using next-generation sequencing. Standard Z-score analysis was used to identify fetal SCAs. NIPT-positive results were confirmed by invasive prenatal diagnosis (IPD). RESULTS: A total of 42,164 pregnant women with singleton pregnancies were recruited in this study. They were divided into the following five groups with different clinical indications: with ultrasound soft index abnormalities (9.23%, 3,892/42,164); with advanced maternal age (22.14%, 9,336/42,164); with high risk for maternal serum screening (MSS) (18.35%, 7,738/42,164); with an intermediate risk for MSS (26.6%, 11,215/42,164); and with low risk (23.68%, 9,983/42,164). In all, 223 women had a high risk for SCAs by NIPT with a positive rate of 0.53%. There was no significant difference associated with the five groups in the positive rate. Of all of the positive results, 89 were 45,X (39.91%), 38 were 47,XXX (17.04%), 31 were 46,XY,del(X) (13.90%), 50 were 47,XXY (22.42%,), and 15 were 47,XYY (6.73%). Finally, 147 participants (65.92%) chose to undergo IPD, and 47 cases were confirmed. The combined positive predictive value (PPV) of NIPT for SCA was 31.97% (47/147). PPV was high for 47,XYY (100%, 11/11), moderate for 47,XXX (42.86%, 9/21) and 47,XXY (45.45%, 15/33), but low for 45,X (16.13%, 10/62) and 46,XY,del(X) (10%, 2/20). The termination rates of Turner syndrome and 47,XXY syndrome were higher than 47,XXX and 47,XYY syndromes. CONCLUSION: In this relatively large cohort, we evaluated the value of NIPT for SCAs. Our data showed that with informed consent and subsequent professional genetical consulting, NIPT can be a useful method to screen SCAs.
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spelling pubmed-88257882022-02-10 Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China Zhao, Ganye Dai, Peng Wang, Conghui Liu, Lina Zhao, Xuechao Kong, Xiangdong Front Med (Lausanne) Medicine BACKGROUND: The relatively high incidence and the clinical symptoms of sex chromosome aneuploidies (SCAs) make prenatal screening of SCAs an attractive option for pregnant women. However, limited studies have assessed the clinical performance of noninvasive prenatal testing (NIPT) for screening SCAs. This study was performed to evaluate the clinical performance of NIPT for SCAs in singleton pregnancies in central China. METHODS: Noninvasive prenatal testing was performed using next-generation sequencing. Standard Z-score analysis was used to identify fetal SCAs. NIPT-positive results were confirmed by invasive prenatal diagnosis (IPD). RESULTS: A total of 42,164 pregnant women with singleton pregnancies were recruited in this study. They were divided into the following five groups with different clinical indications: with ultrasound soft index abnormalities (9.23%, 3,892/42,164); with advanced maternal age (22.14%, 9,336/42,164); with high risk for maternal serum screening (MSS) (18.35%, 7,738/42,164); with an intermediate risk for MSS (26.6%, 11,215/42,164); and with low risk (23.68%, 9,983/42,164). In all, 223 women had a high risk for SCAs by NIPT with a positive rate of 0.53%. There was no significant difference associated with the five groups in the positive rate. Of all of the positive results, 89 were 45,X (39.91%), 38 were 47,XXX (17.04%), 31 were 46,XY,del(X) (13.90%), 50 were 47,XXY (22.42%,), and 15 were 47,XYY (6.73%). Finally, 147 participants (65.92%) chose to undergo IPD, and 47 cases were confirmed. The combined positive predictive value (PPV) of NIPT for SCA was 31.97% (47/147). PPV was high for 47,XYY (100%, 11/11), moderate for 47,XXX (42.86%, 9/21) and 47,XXY (45.45%, 15/33), but low for 45,X (16.13%, 10/62) and 46,XY,del(X) (10%, 2/20). The termination rates of Turner syndrome and 47,XXY syndrome were higher than 47,XXX and 47,XYY syndromes. CONCLUSION: In this relatively large cohort, we evaluated the value of NIPT for SCAs. Our data showed that with informed consent and subsequent professional genetical consulting, NIPT can be a useful method to screen SCAs. Frontiers Media S.A. 2022-01-26 /pmc/articles/PMC8825788/ /pubmed/35155454 http://dx.doi.org/10.3389/fmed.2021.672211 Text en Copyright © 2022 Zhao, Dai, Wang, Liu, Zhao and Kong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Zhao, Ganye
Dai, Peng
Wang, Conghui
Liu, Lina
Zhao, Xuechao
Kong, Xiangdong
Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
title Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
title_full Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
title_fullStr Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
title_full_unstemmed Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
title_short Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
title_sort clinical application of noninvasive prenatal testing for sex chromosome aneuploidies in central china
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825788/
https://www.ncbi.nlm.nih.gov/pubmed/35155454
http://dx.doi.org/10.3389/fmed.2021.672211
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