Application of the BACs‐on‐Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions. Issue 2 (17th January 2018)

• Record Type: Journal Article
• Authors: Huang, Hailong; Zhang, Min; Wang, Yan; Lin, Na; He, Deqin; Chen, Meihuan; Chen, Lingji; Lin, Yuan; Xu, Liangpu
• Is Part Of: Molecular reproduction and development. Volume 85:Issue 2(2018)
• Page Start: 146
• Page End: 154
• Publication Date: 2018-01-17
• Subjects: aneuploidies -- BoBs™ -- karyotyping -- microdeletions -- PND; Reproduction -- Periodicals; Molecular biology -- Periodicals; Molecular genetics -- Periodicals; Embryology -- Periodicals; 571.8
• DOI: 10.1002/mrd.22945
• Languages: English
• ISSNs: 1040-452X

Abstract

Abstract : Prenatal diagnosis focuses on the detection of anatomic and physiologic problems with a foetus before birth. Karyotyping is currently considered the gold standard for prenatal diagnosis of chromosomal abnormalities, but this method can be time consuming. This study evaluated the diagnostic accuracy of the BACs‐on‐Beads TM (BoBs™) assay for the rapid diagnosis of aneuploidies and microdeletions. A total of 625 samples from pregnant women in Fujian province, in southeastern China—including three chorionic villus biopsies, 523 amniotic fluid samples, and 99 umbilical‐cord centesis samples—were assessed for chromosomal abnormalities by karyotyping and by the BoBs™ assay. A diagnosis was successfully achieved by karyotyping for 98.8% (618/625) and by the BoBs™ assay for 100% (625/625) of the samples. Both assays were concordant for trisomy 21 (2.72%, 17/625), trisomy 18 (1.12%, 7/625), trisomy 13 (0.48%, 3/625), and sex chromosome aneuploidies (0.8%, 5/625). Unlike karyotyping, the BoBs™ assay detected 22q11.2 microdeletion (0.64%, 4/625), 22q11.2 microduplication (0.16%, 1/625), Smith–Magenis syndrome microdeletion (0.16%, 1/625), and Miller–Dieker syndrome microdeletion (0.16%, 1/625). Thus, the BoBs™ assay is a reliable and rapid test for detecting common aneuploidies and microdeletions for prenatal diagnosis, and could be used instead of karyotyping for detection of common aneuploidies as well as to provide additional information regarding microdeletions.