Screening and diagnosis of inherited platelet disorders

IF 6.6 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY Critical reviews in clinical laboratory sciences Pub Date : 2022-03-28 DOI:10.1080/10408363.2022.2049199
Alex Bourguignon, S. Tasneem, C. Hayward
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引用次数: 5

Abstract

Abstract Inherited platelet disorders are important conditions that often manifest with bleeding. These disorders have heterogeneous underlying pathologies. Some are syndromic disorders with non-blood phenotypic features, and others are associated with an increased predisposition to developing myelodysplasia and leukemia. Platelet disorders can present with thrombocytopenia, defects in platelet function, or both. As the underlying pathogenesis of inherited thrombocytopenias and platelet function disorders are quite diverse, their evaluation requires a thorough clinical assessment and specialized diagnostic tests, that often challenge diagnostic laboratories. At present, many of the commonly encountered, non-syndromic platelet disorders do not have a defined molecular cause. Nonetheless, significant progress has been made over the past few decades to improve the diagnostic evaluation of inherited platelet disorders, from the assessment of the bleeding history to improved standardization of light transmission aggregometry, which remains a “gold standard” test of platelet function. Some platelet disorder test findings are highly predictive of a bleeding disorder and some show association to symptoms of prolonged bleeding, surgical bleeding, and wound healing problems. Multiple assays can be required to diagnose common and rare platelet disorders, each requiring control of preanalytical, analytical, and post-analytical variables. The laboratory investigations of platelet disorders include evaluations of platelet counts, size, and morphology by light microscopy; assessments for aggregation defects; tests for dense granule deficiency; analyses of granule constituents and their release; platelet protein analysis by immunofluorescent staining or flow cytometry; tests of platelet procoagulant function; evaluations of platelet ultrastructure; high-throughput sequencing and other molecular diagnostic tests. The focus of this article is to review current methods for the diagnostic assessment of platelet function, with a focus on contemporary, best diagnostic laboratory practices, and relationships between clinical and laboratory findings.
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遗传性血小板疾病的筛查和诊断
摘要遗传性血小板疾病是一种常见的出血性疾病。这些疾病具有异质性的潜在病理。一些是具有非血液表型特征的综合征性疾病,另一些则与发展为骨髓发育不良和白血病的易感性增加有关。血小板疾病可表现为血小板减少症、血小板功能缺陷或两者兼有。由于遗传性血小板减少症和血小板功能紊乱的潜在发病机制多种多样,对其进行评估需要进行彻底的临床评估和专门的诊断测试,这通常会对诊断实验室提出挑战。目前,许多常见的非综合征性血小板疾病没有明确的分子病因。尽管如此,在过去几十年中,在改善遗传性血小板疾病的诊断评估方面取得了重大进展,从出血史的评估到提高光透射聚集度的标准化,这仍然是血小板功能的“金标准”测试。一些血小板紊乱测试结果高度预测出血紊乱,一些结果显示与长期出血、手术出血和伤口愈合问题的症状有关。诊断常见和罕见的血小板疾病可能需要多种测定,每种测定都需要控制分析前、分析和分析后的变量。血小板疾病的实验室研究包括通过光学显微镜评估血小板计数、大小和形态;聚合缺陷评估;致密颗粒缺乏试验;颗粒成分及其释放分析;通过免疫荧光染色或流式细胞术进行血小板蛋白分析;血小板促凝功能测试;血小板超微结构评价;高通量测序和其他分子诊断测试。本文的重点是回顾目前血小板功能诊断评估的方法,重点是当代最佳诊断实验室实践,以及临床和实验室结果之间的关系。
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来源期刊
CiteScore
20.00
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: Critical Reviews in Clinical Laboratory Sciences publishes comprehensive and high quality review articles in all areas of clinical laboratory science, including clinical biochemistry, hematology, microbiology, pathology, transfusion medicine, genetics, immunology and molecular diagnostics. The reviews critically evaluate the status of current issues in the selected areas, with a focus on clinical laboratory diagnostics and latest advances. The adjective “critical” implies a balanced synthesis of results and conclusions that are frequently contradictory and controversial.
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