[ACMG变异解读指南的更新影响了听觉神经病患者OTOF基因变异的致病性判断]。

Q4 Medicine
K L Wu, J Li, H Y Wang, Q J Wang
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引用次数: 0

摘要

目的比较美国医学遗传学和基因组学学院(ACMG)和分子病理学协会(AMP)2015年发布的变异解读标准和指南(2015ACMG/AMP指南)与临床基因组资源(ClinGen)耳聋专家组2018年发布的遗传性听力损失(Healing loss,HL)变异解读指南专家规范(2018 HL-EP指南)在评估听觉神经病变患者OTOF基因变异致病性方面的差异。方法:选取38名患有OTOF基因变异的听觉神经病患者作为研究对象(男23名,女15名,年龄0.3-25.9岁)。通过全基因组测序、全外显子组测序或目标区域测序(Panel)结合桑格测序,发现38例患者携带两个以上的OTOF基因突变位点。根据2015年ACMG/AMP指南和2018年HL-EP指南,共对59个候选变异进行了独立解读。与2015 ACMG/AMP指南的判断结果相比,2018 HL-EP指南中被解释为低致病性分类的变异被定义为降级变异,被视为高致病性分类的变异被定义为升级变异。统计分析使用 SPSS 20.0 进行。结果指南间变异分类的一致率为 72.9%(43/59)。在2018 HL-EP指南的分类中,13.6%(8/59)的变异体被升级,13.6%(8/59)的变异体被降级。有几项规则在指南之间存在显著差异(PVS1、PM3、PP2、PP3 和 PP5)。剪接突变的致病性分布存在统计学差异(P=0.013)。结论:2018年HL-EP指南在判断听神经病变患者OTOF基因变异的致病性时,与2015年ACMG/AMP指南不一致。2018年HL-EP指南通过对证据的删减和完善,打破固化思维,使致病性分级更具可追溯性,提高了可信度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The updates of the ACMG variant interpretation guidelines affect the pathogenicity determination of OTOF gene variations in patients with auditory neuropathy].

Objective: To compare the differences between the variation interpretation standards and guidelines issued by the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) in 2015 (The 2015ACMG/AMP guideline) and the Deafness Specialist Group of the Clinical Genome Resource (ClinGen) in 2018 for hereditary hearing loss (Healing loss, HL) issued the expert specification of the variation interpretation guide (The 2018 HL-EP guideline) in evaluating the pathogenicity of OTOF gene variation in patients with auditory neuropathy. Methods: Thirty-eight auditory neuropathy patients with OTOF gene variant were selected as the study subjects (23 males and 15 females, aged 0.3-25.9 years). Using whole-genome sequencing, whole exome sequencing or target region sequencing (Panel) combined with Sanger sequencing, 38 cases were found to carry more than two OTOF mutation sites. A total of 59 candidate variants were independently interpreted based on the 2015 ACMG/AMP guideline and 2018 HL-EP guideline. Compared with the judgment results in 2015 ACMG/AMP guideline, the variants interpreted as lower pathogenic classifications in the 2018 HL-EP guideline were defined as downgraded variants, and the variants regarded as higher pathogenic classifications were defined as upgraded variants. Statistical analysis was conducted using SPSS 20.0. Results: The concordance rate of variant classification between the guidelines was 72.9%(43/59). The 13.6%(8/59) of variants were upgraded and 13.6% (8/59) of variants downgraded in the classifications of the 2018 HL-EP guideline. A couple of rules saw significant differences between the guidelines (PVS1, PM3, PP2, PP3 and PP5). The distribution of pathogenicity of splicing mutation was statistically different (P=0.013). Conclusions: The 2018 HL-EP guideline is inconsistent with the 2015 ACMG/AMP guideline, when judging the pathogenicity of OTOF gene variants in patients with auditory neuropathy. Through the deletion and refinement of evidence and the breaking of solidification thinking, the 2018 HL-EP guideline makes the pathogenicity grading more traceable and improves the credibility.

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CiteScore
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