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类风湿关节炎患者血清中白细胞介素-37水平升高与炎性细胞因子及疾病活动度相关。

Elevated serum levels of Interleukin-37 are associated with inflammatory cytokines and disease activity in rheumatoid arthritis.

作者信息

Yang Libin, Zhang Jun, Tao Jingang, Lu Tan

机构信息

Department of Orthopeadic Surgery, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, Henan, China.

出版信息

APMIS. 2015 Dec;123(12):1025-31. doi: 10.1111/apm.12467.

Abstract

Interleukin-37 (IL-37) is closely associated with several inflammatory diseases. However, the role of IL-37 in the pathogenesis of rheumatoid arthritis (RA) remains unclear. The aim of this study was to assess the associations between serum levels of IL-37 and disease activity, inflammatory cytokines, and bone loss in patients with RA. Serum cytokines levels were examined by Enzyme-linked immunosorbent assay (ELISA). Radiographic bone erosion was assessed using the van der Heijde-modified Sharp score and bone mineral density (BMD) was measured using DXA. Serum IL-37 levels in RA patients were significantly higher than those in HCs (p < 0.001), and were significantly positively correlated with clinical parameters of disease activity and serum levels of IL-17 and IL-23. In addition, serum IL-37 levels were significantly higher in patients with stage IV of radiographic bone erosion than those with stage III and stage I-II, and they were significantly higher in those with osteopenia and osteoporosis than in those with normal BMD. Our results suggest that serum IL-37 levels were increased in patients with RA and were positively associated with disease activity, IL-17/IL-23 and bone loss in RA, suggesting that IL-37 may play a critical role in the pathogenesis of RA.

摘要

白细胞介素-37(IL-37)与多种炎症性疾病密切相关。然而,IL-37在类风湿关节炎(RA)发病机制中的作用仍不清楚。本研究旨在评估RA患者血清IL-37水平与疾病活动度、炎性细胞因子及骨质流失之间的关联。采用酶联免疫吸附测定(ELISA)检测血清细胞因子水平。使用范德海伊德改良夏普评分评估影像学骨侵蚀,并使用双能X线吸收法(DXA)测量骨密度(BMD)。RA患者血清IL-37水平显著高于健康对照者(p < 0.001),且与疾病活动度的临床参数以及IL-17和IL-23的血清水平显著正相关。此外,影像学骨侵蚀IV期患者的血清IL-37水平显著高于III期和I-II期患者,骨量减少和骨质疏松患者的血清IL-37水平显著高于BMD正常者。我们的结果表明,RA患者血清IL-37水平升高,且与RA的疾病活动度、IL-17/IL-23及骨质流失呈正相关,提示IL-37可能在RA发病机制中起关键作用。

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