Department of Cytogenetics, Obstetrics and Gynaeacology, CHI Poissy St Germain, Poissy, France; UVSQ, EA 2493, Versailles, France.
Prenat Diagn. 2011 May;31(5):500-8. doi: 10.1002/pd.2727. Epub 2011 Mar 14.
Molecular cytogenetic techniques on uncultured prenatal samples are the sole tests applied in some countries in cases with advanced maternal age (AMA) or increased risk after prenatal screening. Moreover, there is a trend to perform invasive prenatal diagnosis (PD) during the first trimester before ultrasound manifestations, so new rapid and reliable assays are necessary to investigate microdeletions not detectable with the conventional karyotype. We report the validation study of the prenatal bacterial artificial chromosomes-on-Beads™ (BoBs™ ; CE-IVD), a bead-based multiplex assay detecting chromosomes 13, 18, 21, X/Y aneuploidies and nine microdeletion regions having an overall detection rate of 1/1700.
We retrospectively studied 408 selected samples and prospectively tested 212 consecutive samples ascertained for conventional karyotyping.
We did not find false-positive results. Triploidies were not detected. Maternal cell contamination of male samples up to 90% was unmasked inspecting gonosome profiles. Mosaic conditions at 20 to 30% were revealed. Failures were due to low amount of DNA.
Prenatal BoBs™ is a robust technology for the investigation of fetuses with normal karyotype with or without sonographic abnormalities. Running in parallel with the karyotype analysis, it can be proposed instead of rapid FISH or QF-PCR providing rapid results on common aneuploidies and additional information regarding the microdeletion syndromes.
在一些国家,对于高龄产妇(AMA)或产前筛查后风险增加的病例,应用未培养的产前样本进行分子细胞遗传学技术是唯一的检测方法。此外,在超声表现之前的孕早期进行有创性产前诊断(PD)的趋势越来越明显,因此需要新的快速可靠的检测方法来研究常规核型无法检测到的微缺失。我们报告了产前细菌人工染色体-珠(BoBs;CE-IVD)的验证研究,这是一种基于珠的多重检测方法,可检测 13、18、21、X/Y 非整倍体和 9 个微缺失区域,总体检测率为 1/1700。
我们回顾性研究了 408 例选定的样本,并前瞻性检测了 212 例经常规核型分析确定的连续样本。
我们没有发现假阳性结果。三倍体未被检测到。通过检查性染色体图谱,可揭示高达 90%的男性样本中的母体细胞污染。在 20%至 30%的情况下揭示了嵌合体情况。失败是由于 DNA 数量低。
产前 BoBs 是一种强大的技术,可用于研究具有正常核型和/或超声异常的胎儿。与核型分析并行运行时,它可以替代快速 FISH 或 QF-PCR,提供常见非整倍体的快速结果,并提供关于微缺失综合征的额外信息。