Suppr超能文献

应用新一代测序技术对土耳其特拉凯亚地区青年发病的糖尿病相关基因进行分析。

The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region.

机构信息

Trakya University Faculty of Medicine, Department of Medical Genetics, Edirne, Turkey

Trakya University Faculty of Medicine, Department of Pediatric Endocrinology, Edirne, Turkey

出版信息

J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):320-331. doi: 10.4274/jcrpe.galenos.2021.2020.0285. Epub 2021 Feb 10.

Abstract

OBJECTIVE

The aim of this study was to investigate the molecular basis of maturity-onset diabetes of the young (MODY) by targeted-gene sequencing of 20 genes related to monogenic diabetes, estimate the frequency and describe the clinical characteristics of monogenic diabetes and MODY in the Trakya Region of Turkey.

METHODS

A panel of 20 monogenic diabetes related genes were screened in 61 cases. Illumina NextSeq550 system was used for sequencing. Pathogenicity of the variants were assessed by bioinformatics prediction software programs and segregation analyses.

RESULTS

In 29 (47.5%) cases, 31 pathogenic/likely pathogenic variants in the genes and in 11 (18%) cases, 14 variants of uncertain significance (VUS) in the and genes were identified. There were six different pathogenic/likely pathogenic variants and six different VUS which were novel.

CONCLUSION

This is the first study including molecular studies of twenty monogenic diabetes genes in Turkish cases in the Trakya Region. The results showed that pathogenic variants in the gene are the leading cause of MODY in our population. A high frequency of novel variants (32.4%-12/37) in the current study, suggests that multiple gene analysis provides accurate genetic diagnosis in MODY.

摘要

目的

本研究旨在通过对 20 个与单基因糖尿病相关的基因进行靶向基因测序,探讨青年发病的成年型糖尿病(MODY)的分子基础,评估单基因糖尿病和 MODY 在土耳其特拉基亚地区的频率,并描述其临床特征。

方法

对 61 例患者进行了一组 20 个单基因糖尿病相关基因的检测。使用 Illumina NextSeq550 系统进行测序。通过生物信息学预测软件程序和分离分析评估变异的致病性。

结果

在 29 例(47.5%)患者中,发现了 基因中的 31 个致病性/可能致病性变异,以及 基因中的 14 个意义未明变异(VUS)。其中有 6 种不同的致病性/可能致病性变异和 6 种不同的 VUS 是新发现的。

结论

这是第一项在土耳其特拉基亚地区对 20 个单基因糖尿病基因进行分子研究的研究。结果表明,基因中的致病性变异是导致本人群 MODY 的主要原因。在本研究中,新出现的变异(32.4%-12/37)频率较高,提示多基因分析可提供 MODY 的准确遗传诊断。

相似文献

本文引用的文献

2
Congenital hyperinsulinsim: case report and review of literature.先天性高胰岛素血症:病例报告及文献综述
Pan Afr Med J. 2020 Feb 24;35:53. doi: 10.11604/pamj.2020.35.53.16604. eCollection 2020.

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