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使用游离细胞 DNA 进行 22q11.2 缺失的无创性筛查:获益、局限性和挑战。

Noninvasive screening by cell-free DNA for 22q11.2 deletion: Benefits, limitations, and challenges.

机构信息

Research and Development, Cytogenetics and Medical Genetics Unit, TOMA Advanced Biomedical Assays S.p.A., Busto Arsizio (Varese), Italy.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.

出版信息

Prenat Diagn. 2019 Jan;39(2):70-80. doi: 10.1002/pd.5391. Epub 2019 Jan 10.

Abstract

Cell-free DNA (cfDNA) testing for fetal aneuploidy is one of the most important technical advances in prenatal care. Additional chromosome targets beyond common aneuploidies, including the 22q11.2 microdeletion, are now available because of this clinical testing technology. While there are numerous potential benefits, 22q11.2 microdeletion screening using cfDNA testing also presents significant limitations and pitfalls. Practitioners who are offering this test should provide comprehensive pretest and posttest prenatal counselling. The discussion should include the possibility of an absence of a result, as well as the risk of possible discordance between cfDNA screening results and the actual fetal genetic chromosomal constitution. The goal of this review is to provide an overview of the cfDNA testing technologies for 22q11.2 microdeletions screening, describe the current state of test validation and clinical experience, review "no results" and discordant findings based on differing technologies, and discuss management options.

摘要

游离 DNA(cfDNA)检测胎儿非整倍体是产前护理中最重要的技术进步之一。由于这项临床检测技术,现在可以检测到额外的染色体靶标,包括 22q11.2 微缺失。虽然有许多潜在的好处,但 cfDNA 检测进行 22q11.2 微缺失筛查也存在显著的局限性和陷阱。提供此项检测的医生应该提供全面的检测前和检测后产前咨询。讨论内容应包括可能无结果,以及 cfDNA 筛查结果与胎儿实际遗传染色体结构之间可能存在差异的风险。本综述的目的是概述 cfDNA 检测技术在 22q11.2 微缺失筛查中的应用,描述当前的测试验证和临床经验,根据不同的技术回顾“无结果”和不一致的发现,并讨论管理选择。

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