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淋巴细胞-单核细胞比值与类风湿关节炎疾病活动度的相关性。

The association between the lymphocyte-monocyte ratio and disease activity in rheumatoid arthritis.

机构信息

Department of Clinical Laboratory, Taizhou Hospital of Zhejiang Province, Taizhou Enze Medical Center (Group), 150 Ximen Road, Linhai, Zhejiang Province, China.

Department of Clinical Laboratory, Taizhou Hospital of Zhejiang Province, Wenzhou Medical College, Linhai, Zhejiang Province, China.

出版信息

Clin Rheumatol. 2017 Dec;36(12):2689-2695. doi: 10.1007/s10067-017-3815-2. Epub 2017 Sep 14.

Abstract

The lymphocyte-monocyte ratio (LMR) is a systemic inflammatory marker for prediction of disease development, progress, and survival. Recently, a genome-wide association study identified genetic variations in ITGA4 and HLA-DRB1 that affect the LMR levels and were widely believed to be susceptibility genes for autoimmune diseases, including rheumatoid arthritis (RA). However, the role of LMR in RA patients remains unclear. The LMR level and other laboratory data of 66 RA patients, 163 osteoarthritis (OA) patients, and 131 healthy controls (HC) were compared using binary logistic regression. The correlations between LMR and disease activity and other inflammatory markers were measured using the Spearman rank test. ROC curve analyses assessed the diagnostic accuracy of LMR in RA. The LMR and lymphocyte count were significantly lower in RA patients, whereas the monocyte count was significantly higher relative to the HC group/OA patients (p < 0.01). A decreased LMR has been associated with increased disease activity (p = 0.012). In addition, the DAS28 and traditional inflammatory markers, including ESR, CRP, RDW, PLR, and NLR, and immune-related factors, such as C4, IgA, and IgM, were inversely correlated with LMR, while hemoglobin and albumin were positively correlated with LMR. The ROC curve showed that the area under the curve of LMR was 0.705 (95%CI = 0.630-0.781). The corresponding specificity and sensitivity were 82.82 and 45.45%, respectively. The present study shows that the LMR is an important inflammatory marker which could be used to identify disease activity in RA patients and to distinguish RA from OA patients.

摘要

淋巴细胞-单核细胞比值(LMR)是预测疾病发展、进展和生存的全身性炎症标志物。最近,一项全基因组关联研究确定了 ITGA4 和 HLA-DRB1 中的遗传变异,这些变异影响 LMR 水平,被广泛认为是自身免疫性疾病(包括类风湿关节炎(RA))的易感基因。然而,LMR 在 RA 患者中的作用仍不清楚。使用二项逻辑回归比较了 66 例 RA 患者、163 例骨关节炎(OA)患者和 131 例健康对照者(HC)的 LMR 水平和其他实验室数据。采用 Spearman 秩检验测量 LMR 与疾病活动度和其他炎症标志物的相关性。ROC 曲线分析评估了 LMR 在 RA 中的诊断准确性。RA 患者的 LMR 和淋巴细胞计数显著降低,而单核细胞计数显著高于 HC 组/OA 患者(p<0.01)。降低的 LMR 与疾病活动度增加相关(p=0.012)。此外,DAS28 和传统炎症标志物,包括 ESR、CRP、RDW、PLR 和 NLR,以及免疫相关因素,如 C4、IgA 和 IgM,与 LMR 呈负相关,而血红蛋白和白蛋白与 LMR 呈正相关。ROC 曲线显示 LMR 的曲线下面积为 0.705(95%CI=0.630-0.781)。对应的特异性和敏感性分别为 82.82%和 45.45%。本研究表明,LMR 是一种重要的炎症标志物,可用于识别 RA 患者的疾病活动度,并将 RA 与 OA 患者区分开来。

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