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CYP21A2 基因分型在 21-羟化酶缺乏症儿童中的挑战:使用下一代测序在东南安纳托利亚确定基因型-表型相关性。

Challenges of CYP21A2 genotyping in children with 21-hydroxylase deficiency: determination of genotype-phenotype correlation using next generation sequencing in Southeastern Anatolia.

机构信息

Department of Pediatric Endocrinology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.

Department of Molecular Biology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.

出版信息

J Endocrinol Invest. 2021 Nov;44(11):2395-2405. doi: 10.1007/s40618-021-01546-z. Epub 2021 Mar 6.

Abstract

BACKGROUND/PURPOSE: Although it is known that there is generally a good correlation between genotypes and phenotypes, the number of studies reporting discrepancies has recently increased, exclusively between milder genotypes and their phenotypes due to the complex nature of the CYP21A2 gene and methodological pitfalls. This study aimed to assess CYP21A2 genotyping in children with 21-hydroxylase deficiency (21-OHD) and establish their predictive genotype-phenotype correlation features using a large cohort in Southeastern Anatolia's ethnically diverse population.

METHODS

The patients were classified into three groups: salt-wasting (SW), simple virilizing (SV) and non-classical (NC). The genotypes were categorized into six groups due to residual enzyme activity: null-A-B-C-D-E. CYP21A2 genotyping was performed by sequence-specific primer and sequenced with next generation sequencing (NGS), and the expected phenotypes were compared to the observed phenotypes.

RESULTS

A total of 118 unrelated children with 21-OHD were included in this study (61% SW, 24.5% SV and 14.5% NC). The pathogenic variants were found in 79.5% of 171 mutated alleles (60.2%, 22.2%, and 17.6% in SW, SV and NC, respectively). Patient distribution based on genotype groups was as follows: null-16.1%, A-41.4%, B-6.0%, C-14.4%, E-22%). In2G was the most common pathogenic variant (33.9% of all alleles) and the most common variant in the three phenotype groups (SW-38.8%, SV-22.2% and NC-23.3%). The total genotype-phenotype correlation was 81.5%. The correlations of the null and A groups were 100% and 76.1%, respectively, while it was lower in group B and poor in group C (71.4% and 23.5%, respectively).

CONCLUSION

This study revealed that the concordance rates of the severe genotypes with their phenotypes were good, while those of the milder genotypes were poor. The discrepancies could have resulted from the complex characteristics of 21-OHD genotyping and the limitations of using NGS alone without integrating with other comprehensive methods.

摘要

背景/目的:尽管已知基因型与表型之间通常存在良好的相关性,但最近由于 CYP21A2 基因的复杂性和方法学上的缺陷,仅在轻度基因型与其表型之间报告了越来越多的差异。本研究旨在评估东南安纳托利亚多民族人群中患有 21-羟化酶缺乏症(21-OHD)的儿童的 CYP21A2 基因分型,并利用大样本队列确定其预测基因型-表型相关性特征。

方法

患者分为盐丢失型(SW)、单纯男性化型(SV)和非经典型(NC)三组。由于残留酶活性,基因型分为六组:null-A-B-C-D-E。采用序列特异性引物进行 CYP21A2 基因分型,并采用下一代测序(NGS)进行测序,将预期表型与观察表型进行比较。

结果

本研究共纳入 118 例 21-OHD 无亲缘关系的儿童(61%为 SW,24.5%为 SV,14.5%为 NC)。在 171 个突变等位基因中发现了致病性变异(SW、SV 和 NC 中分别为 60.2%、22.2%和 17.6%)。基于基因型组的患者分布如下:null-16.1%、A-41.4%、B-6.0%、C-14.4%、E-22%)。In2G 是最常见的致病性变异(所有等位基因的 33.9%),也是三种表型组中最常见的变异(SW-38.8%、SV-22.2%和 NC-23.3%)。总基因型-表型相关性为 81.5%。null 和 A 组的相关性分别为 100%和 76.1%,而 B 组和 C 组的相关性较低(分别为 71.4%和 23.5%)。

结论

本研究表明,严重基因型与其表型的一致性率较高,而轻度基因型的一致性率较低。这种差异可能是由于 21-OHD 基因分型的复杂特征以及单独使用 NGS 而不与其他综合方法相结合的局限性所致。

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