Department of Pathology and Immunology, Division of Anatomic and Molecular Pathology, Washington University School of Medicine, St Louis, MO, USA.
Department of Medicine, Washington University School of Medicine, Renal Division, St Louis, MO, USA.
Mod Pathol. 2017 Dec;30(12):1739-1747. doi: 10.1038/modpathol.2017.90. Epub 2017 Jul 28.
Next-generation sequencing is increasingly used for clinical evaluation of patients presenting with thrombotic microangiopathies because it allows for simultaneous interrogation of multiple complement and coagulation pathway genes known to be associated with disease. However, the diagnostic yield is undefined in routine clinical practice. Historic studies relied on case-control cohorts, did not apply current guidelines for variant pathogenicity assessment, and used targeted gene enrichment combined with next-generation sequencing. A clinically enhanced exome, targeting ~54 Mb, was sequenced for 73 patients. Variant analysis and interpretation were performed on genes with biological relevance in thrombotic microangiopathy (C3,CD46, CFB, CFH, CFI, DGKE, and THBD). CFHR3-CFHR1 deletion status was also assessed using multiplex ligation-dependent probe amplification. Variants were classified using American College of Medical Genetics and Genomics guidelines. We identified 5 unique novel and 14 unique rare variants in 25% (18/73) of patients, including a total of 5 pathogenic, 4 likely pathogenic, and 15 variants of uncertain clinical significance. Nine patients had homozygous deletions in CFHR3-CFHR1. The diagnostic yield, defined as the presence of a pathogenic variant, likely pathogenic variant or homozygous deletion of CFHR3-CFHR1, was 25% for all patients tested. Variants of uncertain clinical significance were identified in 21% (15/73) of patients.These results illustrate the expected diagnositic yield in the setting of thrombotic microangiopathies through the application of standardized variant interpretation, and highlight the utility of such an approach. Sequencing a clinically enhanced exome to enable targeted, disease-specific variant analysis is a viable approach. The moderate rate of variants of uncertain clinical significance highlights the paucity of data surrounding the variants in our cohort and illustrates the need for expanded variant curation resources to aid in thrombotic microangiopathy-related disease variant classification.
下一代测序技术越来越多地用于评估出现血栓性微血管病的患者,因为它可以同时检测多种已知与疾病相关的补体和凝血途径基因。然而,在常规临床实践中,其诊断效果尚不确定。历史研究依赖于病例对照队列,未应用当前的致病性变异评估指南,并且使用了靶向基因富集与下一代测序相结合的方法。对 73 名患者进行了临床增强外显子组测序,靶向约 54 Mb。对血栓性微血管病中具有生物学相关性的基因(C3、CD46、CFB、CFH、CFI、DGKE 和 THBD)进行了变异分析和解释。还使用多重连接依赖性探针扩增评估了 CFHR3-CFHR1 缺失状态。使用美国医学遗传学与基因组学学院指南对变异进行分类。在 25%(18/73)的患者中发现了 5 个独特的新变异和 14 个独特的罕见变异,其中包括 5 个致病性变异、4 个可能致病性变异和 15 个不确定临床意义的变异。9 名患者 CFHR3-CFHR1 存在纯合缺失。所有接受测试的患者中,致病性变异、可能致病性变异或 CFHR3-CFHR1 纯合缺失的诊断率为 25%。在 21%(15/73)的患者中发现了不确定临床意义的变异。这些结果说明了在血栓性微血管病中应用标准化变异解释后的预期诊断效果,并突出了这种方法的实用性。对临床增强外显子组进行测序以实现有针对性的、特定于疾病的变异分析是一种可行的方法。不确定临床意义的变异的中等发生率突出了我们队列中变异数据的缺乏,并说明了需要扩展变异管理资源以帮助进行与血栓性微血管病相关疾病的变异分类。