Department of Internal Medicine, General Hospital of Sibenik-Knin County , Sibenik, Croatia.
Department of Laboratory Diagnostics of Inborn Errors of Metabolism, Clinical Department of Laboratory Diagnostics, University Hospital Center Zagreb , Zagreb, Croatia.
Acta Clin Belg. 2021 Feb;76(1):32-39. doi: 10.1080/17843286.2019.1659467. Epub 2019 Aug 27.
Philadelphia-negative chronic myeloproliferative neoplasms (MPNs), essential thrombocythemia (ET), polycythemia vera (PV) and myelofibrosis (MF), are characterized by clonal myeloproliferation and a strong inflammatory atmosphere. YKL-40, expressed in granulocytes, macrophages, megakaryocytes and malignant cells, is an acute phase reactant with an important role in tissue remodeling and atherosclerotic inflammation. The aim of this study was to investigate serum YKL-40 levels in MPNs and to assess its clinical correlations. ELISA test was used to measure serum YKL-40 levels in 111 MPN patients and in 32 healthy controls. Serum YKL-40 levels were higher in ET, post-ET MF, PV, post-PV MF and primary MF patients, when compared to healthy controls (p < 0.001). Higher serum YKL-40 levels were associated with parameters indicative of the increased inflammatory state (higher C-reactive protein, poor performance status, presence of constitutional symptoms and cardiovascular risk factors). Additionally, higher serum YKL-40 levels in MF patients were associated with blast phase disease, lower hemoglobin and higher Dynamic International Prognostic Scoring System score. In the multivariate Cox regression models, higher serum YKL-40 levels in ET and PV patients were independently associated with an increased risk of thrombosis (HR 4.64, p = 0.031) and impaired survival in MF patients (HR 4.31, p = 0.038). These results indicate that higher circulating YKL-40 levels in MPNs might have a pathophysiological role in disease progression and thrombosis development. Assessing circulating YKL-40 could help in identification of ET and PV patients at a high risk of future cardiovascular events and has a good potential for improving prognostication of MF patients.
费城阴性慢性骨髓增生性肿瘤(MPN),包括特发性血小板增多症(ET)、真性红细胞增多症(PV)和骨髓纤维化(MF),其特征为克隆性髓系增殖和强烈的炎症环境。YKL-40 在粒细胞、巨噬细胞、巨核细胞和恶性细胞中表达,是一种急性期反应物,在组织重塑和动脉粥样硬化炎症中具有重要作用。本研究旨在探讨 MPN 患者血清 YKL-40 水平及其临床相关性。采用 ELISA 法检测 111 例 MPN 患者和 32 例健康对照者血清 YKL-40 水平。与健康对照组相比,ET、ET 后 MF、PV、PV 后 MF 和原发性 MF 患者的血清 YKL-40 水平更高(p<0.001)。较高的血清 YKL-40 水平与提示炎症状态增加的参数相关(较高的 C 反应蛋白、较差的体能状态、存在全身症状和心血管危险因素)。此外,MF 患者中较高的血清 YKL-40 水平与急变期疾病、较低的血红蛋白和较高的动态国际预后评分系统评分相关。在多变量 Cox 回归模型中,ET 和 PV 患者较高的血清 YKL-40 水平与血栓形成风险增加(HR 4.64,p=0.031)和 MF 患者生存受损(HR 4.31,p=0.038)独立相关。这些结果表明,MPN 中较高的循环 YKL-40 水平可能在疾病进展和血栓形成发展中具有病理生理学作用。评估循环 YKL-40 有助于识别 ET 和 PV 患者未来发生心血管事件的风险,并具有改善 MF 患者预后的良好潜力。