Barker Tyler, Rogers Victoria E, Henriksen Vanessa T, Aguirre Dale, Trawick Roy H, Rasmussen G Lynn, Momberger Nathan G
The Orthopedic Specialty Hospital, Murray, UT 84107, USA.
The Orthopedic Specialty Hospital, Murray, UT 84107, USA.
Cytokine. 2014 Aug;68(2):133-6. doi: 10.1016/j.cyto.2014.04.004. Epub 2014 Apr 29.
Knee osteoarthritis (OA) is a leading cause of physical disability. At the early stage of knee OA, the increase in synovial fluid cytokine concentrations could contribute to the pathogenesis of OA by degrading articular cartilage. It is unknown, however, if inflammatory cytokines increase systemically at the early or advanced stage of knee OA. The systemic increase of inflammatory cytokines could be detrimental to the endogenous status of micronutrients that protect against excessive inflammation and cytokine-mediated events. The purpose of this study was to test the hypothesis that an increase in serum cytokines associate with a decrease in circulating micronutrients in subjects with early compared to advanced knee OA. Advanced knee OA subjects (n=14) displayed radiographic, pain, and muscular weakness symptoms of knee OA. Early knee OA subjects (n=14) were matched (age, gender, and body mass index) to the advanced OA group and displayed one or two of the aforementioned symptoms of knee OA. Inflammatory cytokines, vitamins C (ascorbic acid), D (25-hydroxyvitamin D), and E (α- and γ-tocopherols), and β-carotene were measured in fasting blood samples. In the early OA group, serum tumor necrosis factor (TNF)-α, interleukin (IL)-5, IL-6, IL-12, and IL-13 concentrations were significantly (all p<0.05) increased. Circulating ascorbic acid, 25-hydroxyvitamin D, α- and γ-tocopherol's, and β-carotene concentrations were not significantly different between groups. Based on these preliminary results, we conclude that the systemic increase of inflammatory cytokines is not associated with a decrease in circulating micronutrients in subjects with early compared to advanced knee OA.
膝关节骨关节炎(OA)是身体残疾的主要原因。在膝关节OA的早期,滑液细胞因子浓度的增加可能通过降解关节软骨而促进OA的发病机制。然而,尚不清楚炎症细胞因子在膝关节OA的早期或晚期是否会全身增加。炎症细胞因子的全身增加可能不利于保护机体免受过度炎症和细胞因子介导事件影响的内源性微量营养素状态。本研究的目的是检验以下假设:与晚期膝关节OA患者相比,早期膝关节OA患者血清细胞因子增加与循环微量营养素减少有关。晚期膝关节OA患者(n = 14)表现出膝关节OA的影像学、疼痛和肌肉无力症状。早期膝关节OA患者(n = 14)在年龄、性别和体重指数方面与晚期OA组相匹配,并且表现出上述膝关节OA症状中的一到两种。在空腹血样中测量炎症细胞因子、维生素C(抗坏血酸)、D(25-羟基维生素D)、E(α-和γ-生育酚)以及β-胡萝卜素。在早期OA组中,血清肿瘤坏死因子(TNF)-α、白细胞介素(IL)-5、IL-6、IL-12和IL-13浓度显著升高(均p<0.05)。两组之间循环抗坏血酸、25-羟基维生素D、α-和γ-生育酚以及β-胡萝卜素浓度无显著差异。基于这些初步结果,我们得出结论:与晚期膝关节OA患者相比,早期膝关节OA患者炎症细胞因子的全身增加与循环微量营养素的减少无关。