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Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis

This study explored the clinical application of karyotype analysis combined with BACs-on-Beads (BoBs) technology in prenatal diagnosis. A total of 558 pregnant women who were admitted to Xuzhou Maternity and Child Health Care Hospital from July 2015 to June 2017 were enrolled in this study. All the...

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Autores principales: Fang, Yuan, Wang, Guangming, Gu, Lize, Wang, Jingjing, Suo, Feng, Gu, Maosheng, Gou, Lingshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125840/
https://www.ncbi.nlm.nih.gov/pubmed/30214511
http://dx.doi.org/10.3892/etm.2018.6574
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author Fang, Yuan
Wang, Guangming
Gu, Lize
Wang, Jingjing
Suo, Feng
Gu, Maosheng
Gou, Lingshan
author_facet Fang, Yuan
Wang, Guangming
Gu, Lize
Wang, Jingjing
Suo, Feng
Gu, Maosheng
Gou, Lingshan
author_sort Fang, Yuan
collection PubMed
description This study explored the clinical application of karyotype analysis combined with BACs-on-Beads (BoBs) technology in prenatal diagnosis. A total of 558 pregnant women who were admitted to Xuzhou Maternity and Child Health Care Hospital from July 2015 to June 2017 were enrolled in this study. All the subjects underwent amniocentesis. BoBs assay was performed for subjects in the observation group, and karyotype analysis was performed for subjects in the control group. The main technical indicators of subjects in the two groups were summarized, and cases of chromosome abnormalities were further evaluated. Clinical follow-up of their pregnancy and neonatal birth was undertaken. Finally, the chromosomal manifestations of these patients were compared with those of normal male and normal female, as well as common chromosomal abnormalities. All 558 pregnant women underwent amniocentesis again. Karyotype analysis combined with BoBs assay of amniotic fluid was performed. Cases of chromosomal abnormalities detected were: 75 cases of trisomy 21, 20 cases of trisomy 18, 1 case of trisomy 13, 27 cases of sex chromosomal abnormalities, 12 cases of balanced chromosome translocation, and 2 cases of chromosome microdeletion. The results indicated that karyotype analysis combined with BoBs technology for prenatal diagnosis was easy to perform, and provided quick results with high accuracy. The two testing methods were complementary to each other, which significantly improved the diagnostic rate of chromosomal abnormalities thus reducing birth defects and guiding continued pregnancy of high-risk pregnant women.
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spelling pubmed-61258402018-09-13 Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis Fang, Yuan Wang, Guangming Gu, Lize Wang, Jingjing Suo, Feng Gu, Maosheng Gou, Lingshan Exp Ther Med Articles This study explored the clinical application of karyotype analysis combined with BACs-on-Beads (BoBs) technology in prenatal diagnosis. A total of 558 pregnant women who were admitted to Xuzhou Maternity and Child Health Care Hospital from July 2015 to June 2017 were enrolled in this study. All the subjects underwent amniocentesis. BoBs assay was performed for subjects in the observation group, and karyotype analysis was performed for subjects in the control group. The main technical indicators of subjects in the two groups were summarized, and cases of chromosome abnormalities were further evaluated. Clinical follow-up of their pregnancy and neonatal birth was undertaken. Finally, the chromosomal manifestations of these patients were compared with those of normal male and normal female, as well as common chromosomal abnormalities. All 558 pregnant women underwent amniocentesis again. Karyotype analysis combined with BoBs assay of amniotic fluid was performed. Cases of chromosomal abnormalities detected were: 75 cases of trisomy 21, 20 cases of trisomy 18, 1 case of trisomy 13, 27 cases of sex chromosomal abnormalities, 12 cases of balanced chromosome translocation, and 2 cases of chromosome microdeletion. The results indicated that karyotype analysis combined with BoBs technology for prenatal diagnosis was easy to perform, and provided quick results with high accuracy. The two testing methods were complementary to each other, which significantly improved the diagnostic rate of chromosomal abnormalities thus reducing birth defects and guiding continued pregnancy of high-risk pregnant women. D.A. Spandidos 2018-10 2018-08-06 /pmc/articles/PMC6125840/ /pubmed/30214511 http://dx.doi.org/10.3892/etm.2018.6574 Text en Copyright: © Fang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Fang, Yuan
Wang, Guangming
Gu, Lize
Wang, Jingjing
Suo, Feng
Gu, Maosheng
Gou, Lingshan
Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
title Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
title_full Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
title_fullStr Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
title_full_unstemmed Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
title_short Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
title_sort application of karyotype analysis combined with bacs-on-beads for prenatal diagnosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125840/
https://www.ncbi.nlm.nih.gov/pubmed/30214511
http://dx.doi.org/10.3892/etm.2018.6574
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