首页> 外文期刊>European journal of clinical investigation >Elevated tryptase levels selectively cluster in myeloid neoplasms: a novel diagnostic approach and screen marker in clinical haematology.
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Elevated tryptase levels selectively cluster in myeloid neoplasms: a novel diagnostic approach and screen marker in clinical haematology.

机译:胰蛋白酶水平升高的类胰蛋白酶选择性聚集:一种新的诊断方法和临床血液学筛查标志物。

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BACKGROUND: Recent data suggest that tryptase, a mast cell enzyme, is expressed in neoplastic cells in myeloid leukaemias. In several of these patients, increased serum tryptase levels are detectable. MATERIALS AND METHODS: We have determined serum tryptase levels in 914 patients with haematological malignancies, including myeloproliferative disorders (n = 156), myelodysplastic syndromes (MDS, n = 241), acute myeloid leukaemia (AML, n = 317), systemic mastocytosis (SM, n = 81), non-Hodgkin's lymphoma (n = 59) and acute lymphoblastic leukaemia (n = 26). Moreover, tryptase was measured in 136 patients with non-neoplastic haematological disorders, 102 with non-haematological disorders and 164 healthy subjects. RESULTS: In healthy subjects, the median serum tryptase was 5.2 ng mL(-1). Elevated serum tryptase levels were found to cluster in myeloid neoplasm, whereas almost all patients with lymphoid neoplasms exhibited normal tryptase. Among myeloid neoplasms, elevated tryptase levels (> 15 ng mL(-1)) were recorded in > 90% of patients with SM, 38% with AML, 34% with CML and 25% with MDS. The highest tryptase levels, often > 1000 ng mL(-1), were found in advanced SM and core-binding-factor leukaemias. In most patients with non-neoplastic haematological disorders and non-haematological disorders analysed in our study, tryptase levels were normal, the exception being a few patients with end-stage kidney disease and helminth infections, in whom a slightly elevated tryptase was found. CONCLUSIONS: In summary, tryptase is a new diagnostic marker of myeloid neoplasms and a useful test in clinical haematology.
机译:背景:最近的数据表明,类胰蛋白酶(一种肥大细胞酶)在髓样白血病的肿瘤细胞中表达。在其中一些患者中,可检测到血清类胰蛋白酶水平升高。材料与方法:我们测定了914例血液系统恶性肿瘤患者的血清类胰蛋白酶水平,包括骨髓增生异常(n = 156),骨髓增生异常综合症(MDS,n = 241),急性髓细胞性白血病(AML,n = 317),系统性肥大细胞增多症( SM,n = 81),非霍奇金淋巴瘤(n = 59)和急性淋巴细胞白血病(n = 26)。此外,在136例非肿瘤性血液疾病患者,102例非血液性疾病患者和164名健康受试者中测量了类胰蛋白酶。结果:在健康受试者中,血清类胰蛋白酶的中位数为5.2 ng mL(-1)。发现血清类胰蛋白酶水平升高,聚集在髓样肿瘤中,而几乎所有淋巴样肿瘤患者均表现出正常的类胰蛋白酶。在骨髓肿瘤中,> 90%的SM患者,38%的AML患者,34%的CML患者和25%的MDS患者的类胰蛋白酶水平升高(> 15 ng mL(-1))。在晚期SM和核心结合因子白血病中发现最高的类胰蛋白酶水平,通常> 1000 ng mL(-1)。在我们研究中分析的大多数非肿瘤性血液学疾病和非血液学疾病患者中,类胰蛋白酶水平正常,只有少数患有终末期肾脏疾病和蠕虫感染的患者,其类胰蛋白酶水平略有升高。结论:综上所述,类胰蛋白酶是骨髓瘤的一种新的诊断标记,是临床血液学中的一项有用测试。

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