Suppr超能文献

应用定制的 NGS 基因 panel 为遗传性共济失调的分子检测提供了高诊断效用。

Application of a custom NGS gene panel revealed a high diagnostic utility for molecular testing of hereditary ataxias.

机构信息

Department of Genetics, Institute of Psychiatry and Neurology, 9 Sobieskiego Street, 02-957, Warsaw, Poland.

Department of Internal Medicine and Gerontology, Faculty of Medicine, Jagiellonian University Medical College, Krakow, Poland.

出版信息

J Appl Genet. 2022 Sep;63(3):513-525. doi: 10.1007/s13353-022-00701-3. Epub 2022 May 19.

Abstract

Hereditary ataxias (HA) are a rare group of heterogeneous disorders. Here, we present the results of molecular testing of a group of ataxia patients using a custom-designed next-generation sequencing (NGS) panel. Due to the genetic and clinical overlapping of hereditary ataxias and spastic paraplegias (HSP), the panel encompasses together HA and HSP genes. The NGS libraries, comprising coding sequences for 152 genes, were performed using KAPA HyperPlus and HyperCap Target Enrichment Kit, sequenced on the MiSeq instrument. The results were analyzed using the BaseSpace Variant Interpreter and Integrative Genomics Viewer. All pathogenic and likely pathogenic variants were confirmed using Sanger sequencing. A total of 29 patients with hereditary ataxias were enrolled in the NGS testing, and 16 patients had a confirmed molecular diagnosis with diagnostic accuracy rate of 55.2%. Pathogenic or likely pathogenic mutations were identified in 10 different genes: POLG (PEOA1, n = 3; SCAE, n = 2), CACNA1A (EA2, n = 2), SACS (ARSACS, n = 2), SLC33A1 (SPG42, n = 2), STUB1 (SCA48, n = 1), SPTBN2 (SCA5, n = 1), TGM6 (SCA35, n = 1), SETX (AOA2, n = 1), ANO10 (SCAR10, n = 1), and SPAST (SPG4, n = 1). We demonstrated that an approach based on the targeted use of the NGS panel can be highly effective and a useful tool in the molecular diagnosis of ataxia patients. Furthermore, we highlight the fact that a sequencing panel targeting both ataxias and HSP genes increases the diagnostic success level.

摘要

遗传性共济失调(HA)是一组罕见的异质性疾病。在这里,我们报告了使用定制设计的下一代测序(NGS)面板对一组共济失调患者进行分子检测的结果。由于遗传性共济失调和痉挛性截瘫(HSP)的遗传和临床重叠,该面板同时包含 HA 和 HSP 基因。NGS 文库包含 152 个基因的编码序列,使用 KAPA HyperPlus 和 HyperCap Target Enrichment Kit 进行制备,在 MiSeq 仪器上进行测序。使用 BaseSpace Variant Interpreter 和 Integrative Genomics Viewer 分析结果。使用 Sanger 测序法对所有致病性和可能致病性的变体进行确认。共有 29 名遗传性共济失调患者接受了 NGS 检测,16 名患者获得了明确的分子诊断,诊断准确率为 55.2%。在 10 个不同的基因中发现了致病性或可能致病性的突变:POLG(PEOA1,n=3;SCAE,n=2)、CACNA1A(EA2,n=2)、SACS(ARSACS,n=2)、SLC33A1(SPG42,n=2)、STUB1(SCA48,n=1)、SPCN2(SCA5,n=1)、TGM6(SCA35,n=1)、SETX(AOA2,n=1)、ANO10(SCAR10,n=1)和 SPAST(SPG4,n=1)。我们证明,基于靶向使用 NGS 面板的方法可以非常有效,并且是分子诊断患者的有用工具。此外,我们强调了一个事实,即针对共济失调和 HSP 基因的测序面板可以提高诊断成功率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验