基于扩增子的新一代定向测序,利用干血点检测46,xy差异/性发育障碍:旨在通过微创检测进行诊断。

IF 1.2 Q4 ENDOCRINOLOGY & METABOLISM
Clinical Pediatric Endocrinology Pub Date : 2025-07-01 Epub Date: 2025-04-04 DOI:10.1297/cpe.2024-0081
Erika Uehara, Kazuhisa Akiba, Keiko Matsubara, Maki Fukami, Kanako Tanase-Nakao
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引用次数: 0

摘要

通过微创检测快速基因诊断性发育差异/障碍(DSD)是可取的。在这项研究中,我们利用22例46,xy DSD患者的干血斑,对AR和SRD5A2进行了基于PCR扩增子的下一代测序(NGS)。我们将结果与使用静脉血来源DNA的外包捕获NGS的结果进行了比较。我们成功地从干燥的血斑中提取DNA,并在至少7天内获得了22例中19例的分析结果。使用干血点的扩增子NGS所需的DNA量明显低于使用静脉血的捕获型NGS(中位数8.7 ng vs. 1434.8 ng)。我们在19例病例中的16例中发现了SRD5A2的4个单核苷酸替换。除病例1外,两次NGS分析和Sanger静脉血测序结果一致。在这种情况下,基于扩增子的NGS使用干燥的血斑错误地将杂合的SRD5A2变异识别为纯合的,可能是由于等位基因缺失。总之,我们证明了基于扩增子的NGS使用干血点可以快速和微创地检测46,xy DSD患者的基因。然而,优化从干血点提取DNA和使用Sanger测序验证检测到的变异是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amplicon-based targeted next-generation sequencing using dried blood spots for 46,XY differences/disorders of sex development: Aiming for diagnosis by minimally invasive testing.

Rapid genetic diagnosis of differences/disorders of sex development (DSD) through minimally invasive testing is desirable. In this study, we performed PCR amplicon-based next-generation sequencing (NGS) targeting AR and SRD5A2 using dried blood spots from 22 patients with 46,XY DSD. We compared the results with those of an outsourced capture-based NGS using venous blood-derived DNA. We successfully extracted DNA from the dried blood spots and obtained analysis results for 19 of the 22 cases within a minimum of seven days. The DNA quantity required was significantly lower for amplicon-based NGS using dried blood spots than for capture-based NGS using venous blood (median 8.7 ng vs. 1434.8 ng). We identified four single-nucleotide substitutions in SRD5A2 in 16 of the 19 cases. The results were consistent between the two NGS analyses and Sanger sequencing using venous blood, except for case 1. In this case, amplicon-based NGS using dried blood spots incorrectly identified a heterozygous SRD5A2 variant as homozygous, presumably due to allelic dropout. In conclusion, we demonstrated that amplicon-based NGS using dried blood spots allowed for rapid and minimally invasive genetic testing in patients with 46,XY DSD. However, optimizing DNA extraction from dried blood spots and validating detected variants using Sanger sequencing are necessary.

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来源期刊
Clinical Pediatric Endocrinology
Clinical Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.40
自引率
7.10%
发文量
34
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