评估新诊断慢性淋巴细胞白血病患者的血浆 CCL3 水平及其与临床和实验室参数的相关性

IF 0.1 Q4 HEMATOLOGY
Ruaa Hameed Nasif, Maysem Mouayad Abd Al-Mahdi
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引用次数: 0

摘要

慢性淋巴细胞白血病(CLL)是成人中最常见的一种白血病,是一种淋巴细胞增生性疾病,其定义是成熟克隆在血液、继发性淋巴组织、脾脏和骨髓中的扩增。CCL3 是一种细胞因子,参与发育、修复和急性炎症状态。因此,CCL3 应有助于对 CLL 患者进行风险评估。 本研究的目的是估算与健康对照组相匹配的新诊断 CLL 患者的血浆 CCL3 水平,并将其与血液学参数、临床参数和预后标志物(如 CD38 和 LAIR-1)相关联。 本研究为横断面研究。患者组包括 55 名经形态学和免疫分型确诊的 CLL 患者,对照组包括 30 名性别和年龄匹配的健康人。使用酶联免疫吸附试验测定血浆中的CCL3水平。统计分析使用 Microsoft Office Excel 2019 和 SPSS 26 版本。正态分布数值的平均值和标准差,而 "中位数 "和 "范围 "则用于描述非正态分布的数值。以 P <0.05 为显著程度。 患者组(中位数水平约为 766.42 ng/ml)和对照组(中位数水平约为 453.35 ng/ml)的 CCL3 之间存在统计学意义上的显著关系(P < 0.001)。CCL3 与白细胞、血红蛋白和绝对淋巴细胞数之间存在很强的相关性(分别为 P = 0.013、P < 0.001 和 P = 0.011)。CCL3的表达与Binet分期和肝肿大有密切关系(分别为P<0.001和P=0.020),但CCL3的表达与CD38和LAIR-1无明显关系。 CLL患者的CCL3水平较高,且随着Binet分期的进展而升高。因此,我们的研究阐明了测量CCL3血浆水平对CLL患者随访和风险评估的有用性和简便性。
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 CCL3 levels in individuals with newly diagnosed chronic lymphocytic leukemia and it’s correlation with clinical and laboratory parameters
The most prevalent type of leukemia in adults is called chronic lymphocytic leukemia (CLL). is a lymphoproliferative condition is defined by the mature clone’s expansion in blood, secondary lymphoid tissues, spleen and the bone marrow. CCL3 is a cytokine that is involved in development, repair, and the acute inflammatory state. CCL3, therefore, should become useful for risk assessment in patients with CLL. The aims of the study were to estimate the level of plasma CCL3 in newly diagnosed patients with CLL matched to healthy controls and correlate it with hematological parameters and clinical parameters and prognostic markers such as CD38 and LAIR-1. This study was cross-sectional in nature. Patient group included 55 patients with newly established diagnosis of CLL proven by morphology and immunophenotyping and control group included sex and age matched of 30 healthy individuals. The plasma CCL3 levels were measured using an enzyme-linked immunosorbent assay. Microsoft Office Excel 2019 and SPSS version 26 were used for the statistical analysis. The mean and standard deviation of normally distributed numerical values whereas the terms “median” and “range” were used to describe numerical values that are not regularly distributed. P <0.05 was used to determine the degree of significance. There were statistically significant relationships between CCL3 of patient (median level about 766.42 ng/ml) and control (median level about 453.35 ng/ml) groups (P < 0.001). There was a strong correlation between CCL3 and white blood cell, hemoglobin, and absolute lymphocyte count (P = 0.013, P < 0.001, and P = 0.011, respectively). There was a strong relationship between CCL3 expression with Binet stage and with hepatomegaly (P < 0.001 and P = 0.020, respectively), but no significant relation between CCL3 expression and CD38 and LAIR-1. Patients with CLL had high levels of CCL3, which increased with advancing Binet stages. Therefore, our research clarified the useful and simplicity of measurement of CCL3 plasma levels for follow-up in CLL patients and risk assessment.
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