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使用 KaryoLite™ BACs-on-Beads™ 检测试剂盒快速检测妊娠产物中的非整倍体。

Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assay.

机构信息

ARUP Institute for Clinical and Experimental Pathology®, ARUP Laboratories, Salt Lake City, UT, USA.

出版信息

Prenat Diagn. 2013 Jan;33(1):25-31. doi: 10.1002/pd.4003. Epub 2012 Nov 8.

Abstract

OBJECTIVE

Chromosome analysis is the traditional method for detecting genetic abnormalities in products of conception, but it is prone to a high failure rate because of the requirement for cell culture. Molecular genetic tests do not require cell culture, but are either more expensive (e.g. chromosomal microarray) or less sensitive than chromosome analysis (e.g. fluorescence in situ hybridization, multiplex ligation mediated amplification). The KaryoLite™ BACs-on-Beads™ (KL-BoBs™) assay is highly multiplexed with low resolution coverage and is designed to detect aneusomy for any chromosome.

METHODS

We retrospectively tested 100 products of conception samples previously characterized by karyotype (n = 90), and/or microarray (n = 61) using KL-BoBs™. We included samples extracted from either cultured or direct specimens from placental villi or fetal somatic tissue, with a variety of chromosomal abnormalities typically identified in our clinical cytogenetics laboratory.

RESULTS

KL-BoBs™ and microarray results were concordant for all cases of aneusomy. On the basis of a review of 3794 consecutive cases in our laboratory, aneusomy accounts for 74.3% of abnormalities detected. Polyploidy and structural abnormalities were not detected by KL-BoBs™.

CONCLUSION

KL-BoBs™ is potentially very useful as a first line test for aneusomy detection because of its lower cost, rapid detection, and ability to generate a molecular karyotype for samples that fail to grow in culture.

摘要

目的

染色体分析是检测妊娠产物遗传异常的传统方法,但由于需要细胞培养,因此容易失败率高。分子遗传学测试不需要细胞培养,但要么比染色体分析更昂贵(例如染色体微阵列),要么灵敏度不如染色体分析(例如荧光原位杂交,多重连接介导的扩增)。KaryoLite™BACs-on-Beads™(KL-BoBs™)检测具有高度多重性和低分辨率覆盖度,旨在检测任何染色体的非整倍体。

方法

我们回顾性地检测了 100 个先前通过核型(n=90)和/或微阵列(n=61)进行特征分析的妊娠产物样本,使用 KL-BoBs™。我们包括了从培养或直接取自胎盘绒毛或胎儿体组织的样本,这些样本具有我们临床细胞遗传学实验室中通常识别的各种染色体异常。

结果

KL-BoBs™和微阵列结果与所有非整倍体病例一致。根据我们实验室的 3794 例连续病例回顾,非整倍体占检测到异常的 74.3%。KL-BoBs™未检测到多倍体和结构异常。

结论

KL-BoBs™因其成本较低、检测速度快以及能够为培养失败的样本生成分子核型,因此作为检测非整倍体的一线检测方法具有很大的潜力。

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