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扩展携带者筛查的临床有效性:评估 200 多种疾病中的基因-疾病关系。

Clinical validity of expanded carrier screening: Evaluating the gene-disease relationship in more than 200 conditions.

机构信息

Myriad Women's Health, Myriad Genetics, South San Francisco, California.

Division of Clinical Genomic Interpretation, Baylor Genetics, Houston, Texas.

出版信息

Hum Mutat. 2020 Aug;41(8):1365-1371. doi: 10.1002/humu.24033. Epub 2020 May 21.

DOI:10.1002/humu.24033
PMID:32383249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7496796/
Abstract

Clinical guidelines consider expanded carrier screening (ECS) to be an acceptable method of carrier screening. However, broader guideline support and payer adoption require evidence for associations between the genes on ECS panels and the conditions for which they aim to identify carriers. We applied a standardized framework for evaluation of gene-disease association to assess the clinical validity of conditions screened by ECS panels. The Clinical Genome Resource (ClinGen) gene curation framework was used to assess genetic and experimental evidence of associations between 208 genes and conditions screened on two commercial ECS panels. Twenty-one conditions were previously classified by ClinGen, and the remaining 187 were evaluated by curation teams at two laboratories. To ensure consistent application of the framework across the laboratories, concordance was evaluated on a subset of conditions. All 208 evaluated conditions met the evidence threshold for supporting a gene-disease association. Furthermore, 203 of 208 (98%) achieved the strongest ("Definitive") level of gene-disease association. All conditions evaluated by both commercial laboratories were similarly classified. Assessment using the ClinGen standardized framework revealed strong evidence of gene-disease association for conditions on two ECS panels. This result establishes the disease-level clinical validity of the panels considered herein.

摘要

临床指南认为扩展携带者筛查(ECS)是一种可接受的携带者筛查方法。然而,更广泛的指南支持和支付方采用需要基因与 ECS 面板上的疾病之间的关联证据,以及它们旨在确定携带者的条件。我们应用了一个评估基因-疾病关联的标准化框架,以评估 ECS 面板筛查的条件的临床有效性。临床基因组资源 (ClinGen) 基因编纂框架用于评估 208 个基因与两个商业 ECS 面板上筛查的条件之间的关联的遗传和实验证据。21 种情况之前由 ClinGen 分类,其余 187 种情况由两个实验室的编纂小组进行评估。为了确保该框架在实验室之间的一致应用,对一组条件进行了一致性评估。所有 208 种评估条件都符合支持基因-疾病关联的证据标准。此外,208 种条件中有 203 种(98%)达到了最强的(“明确”)基因-疾病关联级别。两个商业实验室评估的所有条件都被归类为相同。使用 ClinGen 标准化框架进行评估显示,两个 ECS 面板上的条件与疾病之间存在很强的基因-疾病关联证据。这一结果确立了本文所考虑的面板在疾病层面的临床有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4c/7496796/b7e6d02269ec/HUMU-41-1365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4c/7496796/b7e6d02269ec/HUMU-41-1365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba4c/7496796/b7e6d02269ec/HUMU-41-1365-g001.jpg

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Genet Med. 2020 Mar;22(3):453-461. doi: 10.1038/s41436-019-0666-z. Epub 2019 Nov 16.
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Assessing the strength of evidence for genes implicated in fatty acid oxidation disorders using the ClinGen clinical validity framework.运用 ClinGen 临床有效性框架评估脂肪酸氧化障碍相关基因证据的强度。
Mol Genet Metab. 2019 Sep-Oct;128(1-2):122-128. doi: 10.1016/j.ymgme.2019.07.008. Epub 2019 Jul 18.
3
Inter-lab concordance of variant classifications establishes clinical validity of expanded carrier screening.
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Clin Genet. 2019 Sep;96(3):236-245. doi: 10.1111/cge.13582. Epub 2019 Jul 1.
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ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.ClinGen 对 164 个听力损失基因-疾病对进行专家临床有效性评估。
Genet Med. 2019 Oct;21(10):2239-2247. doi: 10.1038/s41436-019-0487-0. Epub 2019 Mar 21.
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