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[一项登记研究中基于高通量测序的先天性血小板减少症/血小板疾病诊断进展]

[Developments of high-throughput sequencing-based diagnosis of congenital thrombocytopenia/platelet disorders in a registry study].

作者信息

Ishiguro Akira, Uchiyama Toru, Sakamoto Atsushi, Kunishima Shinji

机构信息

Center for Postgraduate Education and Training, National Center for Child Health and Development.

Department of Human Genetics, National Center for Child Health and Development.

出版信息

Rinsho Ketsueki. 2024;65(8):747-755. doi: 10.11406/rinketsu.65.747.

Abstract

Congenital thrombocytopenia/platelet disorders are heterogeneous disorders of platelet number and/or function. Pathogenic variants in the genes implicated in megakaryocyte differentiation and platelet formation cause thrombocytopenia in these patients. Recent advances have elucidated several causative genes for these disorders, but identifying the underlying causative genes remains challenging. Patients with these disorders often receive inappropriate treatments, including glucocorticoids and splenectomy, for chronic immune thrombocytopenia (ITP). In Japan, we have developed a diagnostic system using high-throughput DNA sequencing with a multigene panel and established a registry. Between 2018 and 2023, 245 patients were enrolled and analyzed. Pathogenic variants in 17 genes (42 MYH9, 19 ANKRD26, 17 ITGA2B/ITGB3, 8 ACTN1, 8 WAS, 6 ETV6, 6 VWF, 5 CYCS, and 14 others) were identified in 125 patients (51.0%). An additional 29 patients (11.8%) had suspected pathogenic variants under investigation. We also found that immature platelet fraction (IPF%) is useful in the differential diagnosis because the median IPF% in MYH9 disorders, 48.7%, was significantly higher than in all other groups (chronic ITP, 13.4%; controls, 2.6%). The results of this study provide new insight into congenital thrombocytopenia/platelet disorders.

摘要

先天性血小板减少症/血小板疾病是血小板数量和/或功能的异质性疾病。参与巨核细胞分化和血小板形成的基因中的致病变异导致这些患者出现血小板减少症。最近的进展已经阐明了这些疾病的几个致病基因,但确定潜在的致病基因仍然具有挑战性。患有这些疾病的患者经常接受不适当的治疗,包括用于慢性免疫性血小板减少症(ITP)的糖皮质激素和脾切除术。在日本,我们开发了一种使用多基因panel进行高通量DNA测序的诊断系统,并建立了一个登记处。在2018年至2023年期间,招募并分析了245名患者。在125名患者(51.0%)中鉴定出17个基因(42个MYH9、19个ANKRD26、17个ITGA2B/ITGB3、8个ACTN1、8个WAS、6个ETV6、6个VWF、5个CYCS和14个其他基因)中的致病变异。另外29名患者(11.8%)有正在研究的疑似致病变异。我们还发现未成熟血小板分数(IPF%)在鉴别诊断中很有用,因为MYH9疾病中的IPF%中位数为48.7%,明显高于所有其他组(慢性ITP为13.4%;对照组为2.6%)。这项研究的结果为先天性血小板减少症/血小板疾病提供了新的见解。

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