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Licensed Unlicensed Requires Authentication Published by De Gruyter July 9, 2019

Efficacy of copy-number variation sequencing technology in prenatal diagnosis

  • Xiaoxi Zhao EMAIL logo and Lin Fu

Abstract

Background

Classical karyotyping and copy-number variation sequencing (CNV-seq) are useful methods for the prenatal detection of chromosomal abnormalities. Here, we examined the potential of using a combination of the two methods for improved and accurate diagnosis.

Methods

From February 2013 to January 2018, 64 pregnant women showing indications for fetal chromosomal examination in the affiliated hospital of the Inner Mongolia Medical University were selected for this study. Amniotic fluid was collected and used for karyotype analysis and CNV-seq.

Results

Karyotype analysis of the 64 cases showed that six cases (9.38%) had chromosomal abnormalities. Using CNV-seq, in addition to three cases with numerical abnormalities of chromosomes, 14 cases were detected with CNV, of which five were pathogenic CNV, four were of uncertain clinical significance and five were polymorphic CNV. However, CNV-seq failed to detect one case with sex chromosome mosaicism and a balanced translocation carrier. The rate of abnormal chromosome and CNV detection was 26.56% (17/64) by CNV-seq.

Conclusion

Application of CNV-seq in prenatal diagnosis could allow the detection of submicroscopic chromosomal abnormalities and effectively reduce the birth of children with microdeletion and microduplication syndrome. Additionally, the combined application of karyotype analysis and CNV-seq can effectively improve the detection rate of chromosome abnormalities.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by the Natural Science Foundation of China (81660542) and the Inner Mongolia Natural Science Fund (2018MS08091).

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Peters DG, Yatsenko SA, Surti U, Rajkovic A. Recent advances of genomic testing in perinatal medicine. Semin Perinatol 2015;39:44–54.10.1053/j.semperi.2014.10.009Search in Google Scholar PubMed PubMed Central

2. Parchem JG, Sparks TN, Gosnell K, Norton ME. Utility of chromosomal microarray in anomalous fetuses. Prenatal Diagn 2018;38:140–7.10.1002/pd.5202Search in Google Scholar PubMed PubMed Central

3. Shao L, Shaw CA, Lu XY, Sahoo T, Bacino CA, Lalani SR, et al. Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases. Am J Med Genet A 2008;146A:2242–51.10.1002/ajmg.a.32399Search in Google Scholar PubMed PubMed Central

4. Fiorentino F, Napoletano S, Caiazzo F, Sessa M, Bono S, Spizzichino L, et al. Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities. Eur J Hum Genet 2013;21:725–30.10.1038/ejhg.2012.253Search in Google Scholar PubMed PubMed Central

5. Xu HB, Yang H, Liu G, Chen H. Systematic review of accuracy of prenatal diagnosis for abnormal chromosome diseases by microarray technology. Genet Mol Res 2014;13:9115–21.10.4238/2014.October.31.27Search in Google Scholar PubMed

6. Ferreira JC, Grati FR, Bajaj K, Malvestiti F, Grimi MB, Trotta A, et al. Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indications. Prenat Diagn 2016;36:1146–55.10.1002/pd.4951Search in Google Scholar PubMed

7. Zhang R, Chen X, Wang D, Chen X, Wang C, Zhang Y, et al. Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders. J Int Med Res 2019;47:1169–78.10.1177/0300060518818020Search in Google Scholar PubMed PubMed Central

8. Liang D, Peng Y, Lv W, Deng L, Zhang Y, Li H, et al. Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes. J Mol Diagn 2014;16:519–26.10.1016/j.jmoldx.2014.05.002Search in Google Scholar PubMed

9. Dong Z, Zhang J, Hu P, Chen H, Xu J, Tian Q, et al. Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach. Genet Med 2016;18:940–8.10.1038/gim.2015.199Search in Google Scholar PubMed

10. Xie C, Tammi MT. CNV-seq, a new method to detect copy number variation using high-throughput sequencing. BMC Bioinform 2009;10:1–9.10.1186/1471-2105-10-80Search in Google Scholar PubMed PubMed Central

11. Zhao XX, Gu XY, Wu AN, Yu RX. The detection rate of fetal chromosomal abnormalities in patients with different indications of amniocentesis. Chin J Obstet Gynecol Pediatr 2014;10:766–9.Search in Google Scholar

12. Liang D, Peng Y, Lv W, Deng L, Zhang Y, Li H, et al. Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes. J Mol Diagn 2014;16:519–26.10.1016/j.jmoldx.2014.05.002Search in Google Scholar PubMed

13. Hayes JL, Tzika A, Thygesen H, Berri S, Wood HM, Hewitt S, et al. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation. Genomics 2013;102:174–81.10.1016/j.ygeno.2013.04.006Search in Google Scholar PubMed

14. Wang J, Chen L, Zhou C, Wang L, Xie H, Xiao Y, et al. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing. Am J Obstet Gynecol 2018;219:287.10.1016/j.ajog.2018.05.030Search in Google Scholar PubMed

15. Liu S, Song L, Cram DS, Xiong L, Wang K, Wu R, et al. Traditional karyotyping vs. copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage. Ultrasound Obstet Gynecol 2015;46:472–7.10.1002/uog.14849Search in Google Scholar PubMed

16. South ST, Chen Z, Brothman AR. Genomic medicine in prenatal diagnosis. Clin Obstet Gynecol 2008;51:62–73.10.1097/GRF.0b013e3181616509Search in Google Scholar PubMed

17. Cohen K, Tzika A, Wood H, Berri S, Robet P, Mason G, et al. Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing. Ultrasound Obstet Gynecol 2015;45:394–401.10.1002/uog.14767Search in Google Scholar PubMed

18. Schmid M, Stary S, Springer S, Bettelheim D, Husslein P, Streubel B, et al. Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study. Ultrasound Obstet Gynecol 2013;41:267–73.10.1002/uog.12389Search in Google Scholar PubMed

Received: 2019-01-04
Accepted: 2019-06-05
Published Online: 2019-07-09
Published in Print: 2019-08-27

© 2019 Walter de Gruyter GmbH, Berlin/Boston

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