Paula Frid, Josefine M Halbig, Per Alstergren, Johanna Rykke Berstad, Lena Cetrelli, Astrid Jullumstrø Feuerherm, Berit Flatø, Annika Rosen, Karen Rosendahl, Marite Rygg, Veronika Rypdal, Nils-Thomas Songstad, Berit Tømmerås, Ellen Nordal, Mohammed Al-Haroni
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Data on demographics, disease activity, presence of TMJ arthritis, and medication were obtained. Samples of unstimulated saliva, serum, and TMJ synovial fluid were collected. The amount of recovered synovial fluid in each sample, collected by the push-and-pull technique, was quantified with the hydroxocobalamin method. Cytokine levels were analyzed using Luminex xMAP technology.</p><p><strong>Results: </strong>Fifteen patients with JIA and TMJ arthritis (JIA-TMJ) (median age 15.0 (interquartile range (IQR) 11.0-16.0) years) and 34 controls (median age 13.0 (IQR 9.8-15.0) years) were consecutively recruited. Samples of saliva (JIA-TMJ, n = 13, and controls, n = 28), serum (JIA-TMJ, n = 11, and controls, n = 16), and TMJ synovial fluid (JIA-TMJ, n = 8) were collected. In saliva from JIA-TMJ, we found significantly higher levels of the cytokines IL-1β, IL-4, IL-5, IL-9, IL-10, IL-12, IL-13, IL-17, Eotaxin, FGF basic, GM CSF, PDGF bb, TNF, and RANTES, while IP-10 was found in significantly lower concentration compared to controls. In serum, there were no significant differences in these cytokine concentrations between JIA-TMJ and controls. Three TMJ synovial samples fulfilled the strict sampling criteria and were included in the analysis. The level of detected cytokines in TMJ synovial samples was higher in JIA-TMJ compared to controls, as described in a previous Nordic study.</p><p><strong>Conclusions: </strong>In this exploratory study, several proinflammatory cytokines were found in higher concentrations in saliva in JIA-TMJ compared to saliva from the controls. No differences were seen in serum between the groups. 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Cytokine levels were analyzed using Luminex xMAP technology.</p><p><strong>Results: </strong>Fifteen patients with JIA and TMJ arthritis (JIA-TMJ) (median age 15.0 (interquartile range (IQR) 11.0-16.0) years) and 34 controls (median age 13.0 (IQR 9.8-15.0) years) were consecutively recruited. Samples of saliva (JIA-TMJ, n = 13, and controls, n = 28), serum (JIA-TMJ, n = 11, and controls, n = 16), and TMJ synovial fluid (JIA-TMJ, n = 8) were collected. In saliva from JIA-TMJ, we found significantly higher levels of the cytokines IL-1β, IL-4, IL-5, IL-9, IL-10, IL-12, IL-13, IL-17, Eotaxin, FGF basic, GM CSF, PDGF bb, TNF, and RANTES, while IP-10 was found in significantly lower concentration compared to controls. In serum, there were no significant differences in these cytokine concentrations between JIA-TMJ and controls. Three TMJ synovial samples fulfilled the strict sampling criteria and were included in the analysis. 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引用次数: 0
摘要
背景:促炎细胞因子是炎症性慢性疾病发病机制的核心,也是重要的治疗靶点。本探索性研究旨在比较幼年特发性关节炎(JIA)和对照组儿童唾液、血清和颞下颌关节(TMJ)滑液中细胞因子的浓度。方法:在这项横断面研究中,我们纳入了来自挪威三个不同中心的JIA和TMJ关节炎的连续儿童,计划进行TMJ皮质类固醇注射,以及非JIA对照组。获得了人口统计学、疾病活动性、TMJ关节炎的存在和药物方面的数据。采集未受刺激的唾液、血清和颞下颌关节滑液样本。每个样品中回收的滑液量,通过推拉技术收集,用羟钴胺素法定量。采用Luminex xMAP技术分析细胞因子水平。结果:连续招募JIA合并TMJ关节炎患者(JIA-TMJ) 15例(中位年龄15.0(四分位间距(IQR) 11.0-16.0)岁),对照组34例(中位年龄13.0 (IQR) 9.8-15.0)岁)。采集唾液样本(JIA-TMJ, n = 13,对照组,n = 28)、血清样本(JIA-TMJ, n = 11,对照组,n = 16)和TMJ滑液样本(JIA-TMJ, n = 8)。在JIA-TMJ的唾液中,我们发现细胞因子IL-1β、IL-4、IL-5、IL-9、IL-10、IL-12、IL-13、IL-17、Eotaxin、FGF basic、GM CSF、PDGF bb、TNF和RANTES的水平显著高于对照组,而IP-10的浓度显著低于对照组。在血清中,JIA-TMJ与对照组之间这些细胞因子浓度无显著差异。三个TMJ滑膜样本符合严格的采样标准并纳入分析。如北欧先前的一项研究所述,JIA-TMJ患者的TMJ滑膜样本中检测到的细胞因子水平高于对照组。结论:在这项探索性研究中,JIA-TMJ患者唾液中几种促炎细胞因子的浓度高于对照组。两组间血清无明显差异。JIA-TMJ滑液中检测到的一些促炎性和抗炎性细胞因子的浓度高于健康成人参考数据的TMJ滑液。
Cytokines in saliva, serum, and temporomandibular joint synovial fluid in children with juvenile idiopathic arthritis: An explorative cross-sectional study.
Background: Proinflammatory cytokines are central to disease mechanisms and important therapeutic targets in inflammatory chronic diseases. This exploratory study aimed to compare cytokine concentrations in saliva, serum, and temporomandibular joint (TMJ) synovial fluid in children with juvenile idiopathic arthritis (JIA) and controls.
Methods: In this cross-sectional study, we included consecutive children with JIA and TMJ arthritis, planned for a TMJ corticosteroid injection, and non-JIA controls from three different centers in Norway. Data on demographics, disease activity, presence of TMJ arthritis, and medication were obtained. Samples of unstimulated saliva, serum, and TMJ synovial fluid were collected. The amount of recovered synovial fluid in each sample, collected by the push-and-pull technique, was quantified with the hydroxocobalamin method. Cytokine levels were analyzed using Luminex xMAP technology.
Results: Fifteen patients with JIA and TMJ arthritis (JIA-TMJ) (median age 15.0 (interquartile range (IQR) 11.0-16.0) years) and 34 controls (median age 13.0 (IQR 9.8-15.0) years) were consecutively recruited. Samples of saliva (JIA-TMJ, n = 13, and controls, n = 28), serum (JIA-TMJ, n = 11, and controls, n = 16), and TMJ synovial fluid (JIA-TMJ, n = 8) were collected. In saliva from JIA-TMJ, we found significantly higher levels of the cytokines IL-1β, IL-4, IL-5, IL-9, IL-10, IL-12, IL-13, IL-17, Eotaxin, FGF basic, GM CSF, PDGF bb, TNF, and RANTES, while IP-10 was found in significantly lower concentration compared to controls. In serum, there were no significant differences in these cytokine concentrations between JIA-TMJ and controls. Three TMJ synovial samples fulfilled the strict sampling criteria and were included in the analysis. The level of detected cytokines in TMJ synovial samples was higher in JIA-TMJ compared to controls, as described in a previous Nordic study.
Conclusions: In this exploratory study, several proinflammatory cytokines were found in higher concentrations in saliva in JIA-TMJ compared to saliva from the controls. No differences were seen in serum between the groups. Some pro- and anti-inflammatory cytokines detected in JIA-TMJ synovial fluid were found in higher concentrations compared to TMJ synovial fluid from healthy adult reference data.
期刊介绍:
Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects.
The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.