Literature DB >> 27977861

A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens.

Songchang Chen1,2, Deyuan Liu3, Junyu Zhang1,2, Shuyuan Li1,2, Lanlan Zhang2, Jianxia Fan2, Yuqin Luo4, Yeqing Qian4, Hefeng Huang1,2,5, Chao Liu3, Huanhuan Zhu3, Zhengwen Jiang3, Chenming Xu1,2,5.   

Abstract

OBJECTIVE: Chromosomal abnormalities such as aneuploidy have been shown to be responsible for causing spontaneous abortion. Genetic evaluation of abortions is currently underperformed. Screening for aneuploidy in the products of conception can help determine the etiology. We designed a high-throughput ligation-dependent probe amplification (HLPA) assay to examine aneuploidy of 24 chromosomes in miscarriage tissues and aimed to validate the performance of this technique.
METHODS: We carried out aneuploidy screening in 98 fetal tissue samples collected from female subjects with singleton pregnancies who experienced spontaneous abortion. The mean maternal age was 31.6 years (range: 24-43), and the mean gestational age was 10.2 weeks (range: 4.6-14.1). HLPA was performed in parallel with array comparative genomic hybridization, which is the gold standard for aneuploidy detection in clinical practices. The results from the two platforms were compared.
RESULTS: Forty-nine out of ninety-eight samples were found to be aneuploid. HLPA showed concordance with array comparative genomic hybridization in diagnosing aneuploidy.
CONCLUSION: High-throughput ligation-dependent probe amplification is a rapid and accurate method for aneuploidy detection. It can be used as a cost-effective screening procedure in clinical spontaneous abortions.
© 2016 John Wiley & Sons, Ltd. © 2016 John Wiley & Sons, Ltd.

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Year:  2017        PMID: 27977861     DOI: 10.1002/pd.4986

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  4 in total

1.  Genetic analysis of products of conception using a HLPA/SNP-array strategy.

Authors:  Jun Mao; Huiling Wang; Haibo Li; Xiaoyan Song; Ting Wang; Jingjing Xiang; Hong Li
Journal:  Mol Cytogenet       Date:  2019-09-02       Impact factor: 2.009

2.  Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissue.

Authors:  Qian Geng; Xiaoli Cui; Yaqi Zhang; Lijuan Zhang; Cai Zhang; Kai Wang; Jianguo Chen; Qingyan Zhu; Jiansheng Xie; Zhiyong Xu; Yang Liu; MengMeng Zhang; Lijie Ding; Wenyong Zhang; Chuanchun Yang
Journal:  J Assist Reprod Genet       Date:  2019-11-13       Impact factor: 3.412

3.  The Second Case of Non-Mosaic Trisomy of Chromosome 26 with Homologous Fusion 26q;26q in the Horse.

Authors:  Sharmila Ghosh; Josefina Kjöllerström; Laurie Metcalfe; Stephen Reed; Rytis Juras; Terje Raudsepp
Journal:  Animals (Basel)       Date:  2022-03-22       Impact factor: 2.752

4.  Whole genome analysis reveals aneuploidies in early pregnancy loss in the horse.

Authors:  Anne Kahler; Brian W Davis; Charlotte A Shilton; James R Crabtree; James Crowhurst; Andrew J McGladdery; D Claire Wathes; Terje Raudsepp; Amanda M de Mestre
Journal:  Sci Rep       Date:  2020-08-07       Impact factor: 4.379

  4 in total

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