成年急性髓性白血病患者血浆前颗粒蛋白水平的评价及其对预后的影响

IF 0.1 Q4 HEMATOLOGY
F. Hussein, A. Ahmed
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引用次数: 0

摘要

背景:急性髓性白血病(AML)是一种造血组织的克隆性恶性疾病,其特征是母细胞积聚,主要在骨髓中,正常血细胞的产生受损。前颗粒蛋白(PGRN)是一种与肿瘤发生、发展、炎症和修复有关的多功能分泌糖蛋白。据报道,高PGRN表达是许多类型的非血液学和有限血液学恶性肿瘤的预后标志物。研究目的:探讨PGRN在新生急性髓系白血病成年患者中的水平及其预后意义。患者、材料和方法:本横断面分析研究对医学城巴格达教学医院血液科2021年12月至2022年10月新诊断的60例成年新发AML患者进行了研究。本研究共纳入28名健康个体作为对照组。诊断是基于在巴格达医学城国家教学实验室中心对外周血和/或骨髓抽吸样本的形态学、免疫表型和遗传学研究。采用PGRN ELISA试剂盒,采用双夹心酶联免疫吸附法(ELISA)检测血浆PGRN水平。结果:AML患者血浆PGRN水平显著高于对照组,未达到缓解的患者血浆PGRN水平也高于对照组。血浆PGRN水平与外周细胞和骨髓细胞百分比呈正相关,与年龄、性别、白细胞总数、血红蛋白水平和血小板水平相关性不显著。M3组与非M3组血浆PGRN水平中位数差异有统计学意义。结论:AML患者诊断时PGRN水平高于对照组,治疗反应较差患者血浆PGRN水平更高,可能作为这些患者的独立危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of plasma progranulin level and the estimation of its prognostic role in adult patients with de novo acute myeloid leukemia
BACKGROUND: Acute Myeloid leukemia (AML) is a clonal, malignant disease of hematopoietic tissues that is characterized by the accumulation of blast cells, principally in the marrow, and impaired production of normal blood cells. Progranulin (PGRN) is a multifunctional secreted glycoprotein implicated in tumorigenesis, development, inflammation, and repair. High PGRN expression was reported as a prognostic marker in many types of nonhematological and limited hematological malignancies. AIM OF STUDY: To evaluate the level and prognostic significance of PGRN in adult patients with de novo acute myeloid leukemia. PATIENTS, MATERIALS AND METHODS: This analytic cross-sectional study was conducted on 60 adult de novo AML patients who were newly diagnosed from December 2021 to October 2022 in the Haematology Department of Baghdad Teaching Hospital in Medical City. A total of 28 healthy individuals were included in this study as a control group. The diagnosis was based on morphology, immunophenotyping, and genetic studies of the peripheral blood and/or bone marrow aspirate samples in the National Center of Teaching Laboratories of the Medical City in Baghdad. Measurement of plasma PGRN level was done by double-sandwich enzyme-linked immunosorbent assay (ELISA) technique using PGRN ELISA kit. RESULTS: Plasma PGRN level was significantly higher in AML patients than in controls, and also was higher in patients who did not achieve remission. Plasma PGRN level shows a strong positive correlation with the peripheral and bone marrow blast percentages and insignificant correlation with age, gender, total leukocyte count, hemoglobin level, and platelets. There was a statistically significant difference in the median of plasma PGRN level between M3 and non-M3 groups. CONCLUSIONS: PGRN is higher in AML patients at diagnosis than in the control group, with plasma level more in those with poor response to treatment and may be used as an independent risk factor in those patients.
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