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意义未明的变异(VUS)重新分类对生殖决策的影响。

The impact of VUS reclassification on reproductive decision making.

作者信息

Peyser Alexandra, Onel Kenan, Hershlag Avner

机构信息

Northwell, New Hyde Park, New York; Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, North Shore University Hospital, Manhasset, New York; Zucker School of Medicine, Uniondale, New York, United States of America.

Roswell Park Comprehensive Cancer Center, Buffalo, New York, United States of America.

出版信息

PLoS One. 2025 May 27;20(5):e0308771. doi: 10.1371/journal.pone.0308771. eCollection 2025.

Abstract

INTRODUCTION

Laboratories will occasionally reclassify a VUS to pathogenic (P) or likely pathogenic (LP), making it clinically actionable. Here, we aim to characterize the frequency of this reclassification in genes tested routinely during preconception counseling in order to help guide reproductive decision making.

DESIGN

Utilizing the American College of Medical Genetics (ACMG) 113-gene pre-conception panel, we conducted data analysis from ClinVar Miner (https://clinvarminer.genetics.utah.edu/). The numbers of VUS's reported for each gene were recorded over a 3-year period (2019, 2021, & 2022). In addition, data on the number of VUS's in conflict (VUS/P and VUS/LP) were recorded. The 10 genes with the most VUS's and the genes with the most frequent reporting discordance were compared over the 3 years.

RESULTS

There was a 103% increase in the number of VUS's reported (2019: 13,278, 2021: 22,434, 2022: 26,965) and a 235% increase in the number of VUS's in conflict (2019:387, 2021: 946, 2022:1297). The overall percent conflict increased significantly (2019: 2.9% vs. 2022: 4.8%). Nine genes among the top 10 with the most frequent VUS's remained the same over the 3-year period, while five out of the ten most frequent genes with VUS's in conflict remained the same.

CONCLUSIONS

The rate of conflicting reporting of a VUS has increased in 3 years and is currently at 4.8%. A potential upgrade of a VUS to pathogenic or likely pathogenic may turn the variant "actionable," justifying testing embryos for the variant through PGT-M.

摘要

引言

实验室偶尔会将意义未明的变异(VUS)重新分类为致病(P)或可能致病(LP),使其具有临床可操作性。在此,我们旨在描述在孕前咨询常规检测基因中这种重新分类的频率,以帮助指导生殖决策。

设计

利用美国医学遗传学学会(ACMG)的113基因孕前检测panel,我们对ClinVar Miner(https://clinvarminer.genetics.utah.edu/)进行了数据分析。记录了3年期间(2019年、2021年和2022年)每个基因报告的VUS数量。此外,还记录了存在冲突的VUS数量(VUS/P和VUS/LP)的数据。比较了3年中VUS数量最多的10个基因和报告不一致最频繁的基因。

结果

报告的VUS数量增加了103%(2019年:13278,2021年:22434,2022年:26965),存在冲突的VUS数量增加了235%(2019年:387,2021年:946,2022年:1297)。总体冲突百分比显著增加(2019年:2.9%对2022年:4.8%)。VUS数量最多的前10个基因中有9个在3年期间保持不变,而存在冲突的VUS数量最多的10个基因中有5个保持不变。

结论

VUS冲突报告率在3年中有所增加,目前为4.8%。VUS潜在升级为致病或可能致病可能会使该变异具有“可操作性”,从而有理由通过胚胎植入前基因检测(PGT-M)对胚胎进行该变异的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312d/12111534/8be12690adf5/pone.0308771.g001.jpg

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