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经济高效且可扩展的克隆性造血检测可深入了解克隆动力学。

Cost-Effective and Scalable Clonal Hematopoiesis Assay Provides Insight into Clonal Dynamics.

机构信息

Vanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, Tennessee.

Department of Medicine, Queen's University, Kingston, Ontario, Canada.

出版信息

J Mol Diagn. 2024 Jul;26(7):563-573. doi: 10.1016/j.jmoldx.2024.03.007. Epub 2024 Apr 6.

DOI:10.1016/j.jmoldx.2024.03.007
PMID:38588769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11536471/
Abstract

Clonal hematopoiesis of indeterminate potential (CHIP) is a common age-related phenomenon in which hematopoietic stem cells acquire mutations in a select set of genes commonly mutated in myeloid neoplasia which then expand clonally. Current sequencing assays to detect CHIP mutations are not optimized for the detection of these variants and can be cost-prohibitive when applied to large cohorts or to serial sequencing. In this study, an affordable (approximately US $8 per sample), accurate, and scalable sequencing assay for CHIP is introduced and validated. The efficacy of the assay was demonstrated by identifying CHIP mutations in a cohort of 456 individuals with DNA collected at multiple time points in Vanderbilt University's biobank and quantifying clonal expansion rates over time. A total of 101 individuals with CHIP/clonal cytopenia of undetermined significance were identified, and individual-level clonal expansion rate was calculated using the variant allele fraction at both time points. Differences in clonal expansion rate by driver gene were observed, but there was also significant individual-level heterogeneity, emphasizing the multifactorial nature of clonal expansion. Additionally, mutation co-occurrence and clonal competition between multiple driver mutations were explored.

摘要

不定潜能的克隆性造血 (CHIP) 是一种常见的与年龄相关的现象,其中造血干细胞在一组常见于髓系肿瘤的基因中获得突变,然后进行克隆性扩增。目前用于检测 CHIP 突变的测序检测方法不能针对这些变体进行优化,并且当应用于大样本量或连续测序时,成本可能过高。在这项研究中,介绍并验证了一种经济实惠(每个样本约 8 美元)、准确且可扩展的 CHIP 测序检测方法。该检测方法的功效通过在范德比尔特大学生物库中对 456 名个体的 DNA 进行多次时间点采集的队列中鉴定 CHIP 突变并量化随时间推移的克隆扩增率来证明。共鉴定出 101 例具有 CHIP/不确定意义的克隆性血细胞减少症的个体,并使用两个时间点的变异等位基因分数计算个体水平的克隆扩增率。观察到驱动基因的克隆扩增率存在差异,但也存在明显的个体水平异质性,强调了克隆扩增的多因素性质。此外,还探讨了多个驱动突变之间的突变共发生和克隆竞争。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/62e760c5b731/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/dc0e2289c332/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/d69af90cdbec/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/463494796e9c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/62e760c5b731/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/dc0e2289c332/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/d69af90cdbec/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/463494796e9c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1152/11536471/62e760c5b731/gr4.jpg

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