需要修订ACMG/AMP解释x连锁变异的指南。

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL Intractable & rare diseases research Pub Date : 2022-08-01 DOI:10.5582/irdr.2022.01067
Yoko Inoue, Osamu Machida, Yosuke Kita, Toshiyuki Yamamoto
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引用次数: 0

摘要

美国医学遗传学和基因组学学院(ACMG)和分子病理学协会(AMP) (ACMG/AMP指南)提供的指南提出了临床变异分类的框架。然而,解释可能是不一致的,每个定义有时被证明是模棱两可的。特别是,解释与x连锁隐性性状相关的变异可能会有困难。为了确认遗传性状的解释是否存在偏差,我们重新分析了在ACMG/AMP指南发布之前报道的变异。正如预期的那样,与x连锁隐性性状相关的变异被解释为致病或可能致病的比例显著降低。因此,在评估与x连锁隐性性状相关的变异时,需要考虑该变异是否仅在男性中根据x连锁隐性性状被识别。应修改ACMG/AMP指南以消除本研究中发现的偏倚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Need for revision of the ACMG/AMP guidelines for interpretation of X-linked variants.

The guidelines provided by American College of Medical Genetics and Genomics (ACMG) and the Association of Molecular Pathology (AMP) (ACMG/AMP guidelines) suggest a framework for the classification of clinical variants. However, the interpretations can be inconsistent, with each definition sometimes proving to be ambiguous. In particular, there can be difficulty with interpretation of variants related to the X-linked recessive trait. To confirm whether there are biases in the interpretation of inherited traits, we reanalyzed variants reported prior to the release of the ACMG/AMP guidelines. As expected, the interpretation ratio as pathogenic or likely pathogenic was significantly lower for variants related to the X-linked recessive trait. Evaluation of variants related to the X-linked recessive trait, hence, need to consider whether the variant is identified only in males in accordance with the X-linked recessive trait. The ACMG/AMP guidelines should be revised to eliminate the bias revealed in this study.

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来源期刊
Intractable & rare diseases research
Intractable & rare diseases research MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
29
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