Serum Inflammatory Markers in Patients With Knee Osteoarthritis A Proteomic Approach

被引:35
|
作者
Giordano, Rocco [1 ]
Petersen, Kristian K. [1 ,2 ]
Andersen, Hjalte H. [2 ]
Simonsen, Ole [3 ]
Arendt-Nielsen, Lars [1 ,2 ]
机构
[1] Ctr Neuroplast & Pain CNAP, Dept Hlth Sci & Technol, Sensory Motor Interact, Aalborg, Denmark
[2] Aalborg Univ, Fac Med, Ctr Sensory Motor Interact SMI, Dept Hlth Sci & Technol, Fredrik Bajers Vej 7D3, DK-9220 Aalborg, Denmark
[3] Aalborg Univ Hosp, Orthoped Surg Res Unit, Aalborg, Denmark
来源
CLINICAL JOURNAL OF PAIN | 2020年 / 36卷 / 04期
基金
新加坡国家研究基金会;
关键词
knee osteoarthritis; inflammation biomarker; pain; proteomics; WNT SIGNALING PATHWAY; SYNOVIAL-FLUID; OLDER-ADULTS; PAIN; ACTIVATION; RECEPTOR; SIRT2; ASSOCIATION; INHIBITION; EXPRESSION;
D O I
10.1097/AJP.0000000000000804
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Objectives: Osteoarthritis (OA) is known to be a slowly progressive disease that alters all tissue compartments of the joint involved with a characteristic degradation of the cartilage, bone remodeling, and inflammation. One of the prominent symptoms in OA patients is pain, but a few radiologic, inflammatory, or structurally related biomarkers have shown few if any associations with pain. This study aimed to assess serum levels of 92 markers involved in inflammatory pathways in patients with knee osteoarthritis (KOA) and evaluate their possible associations with the clinical pain intensity. Materials and Methods: Serum samples were collected from 127 KOA patients and 39 healthy participants with no knee pain. Each serum sample was analyzed for 92 inflammatory markers using the Proximity Extension Array (PEA) technology. Clinical pain intensity was assessed using a Visual Analog Scale, and patients completed the Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire. Results: Fifteen markers were significantly different when comparing KOA patients and healthy participants. Two markers, fibroblast growth factor-21 and Eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1), correlated positively with pain intensity (R=0.235, P=0.008; R=0.233, P=0.008). Moreover, a linear regression model showed interleukin-6, macrophage colony-stimulating factor 1, fibroblast growth factor-21, and tumor necrosis factor superfamily member 12 (TWEAK) as significant independent parameters for pain intensity. Discussion: The associations between specific cytokines and KOA pain intensities provide new insights into the understanding of the underlying factors driving the pain in OA.
引用
收藏
页码:229 / 237
页数:9
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