Ab0917 age Plays a Crucial Role in Crystal Arthritis Severity – A Synovial Fluid Study

Abstract

Background:Incidence and severity of gout and calcium pyrophosphate deposition disease (CPPD) increase with age (1). Aging is associated with immune senescence, leading to a deregulation of the innate immune system and hence inflammation (2). MRI studies hinted on a significantly higher synovial inflammation in older compared to younger arthritis patients(3). Whether inflammatory responses to synovial crystals are more pronounced in elderly patients or not is unknown.Objectives:To test the hypothesis whether aging associates with a more pronounced synovial inflammation in response to urate and CPP crystals.Methods:Gout or CPPD patients with a synovial fluid (SF) aspiration were included. Clinical, blood and synovial parameters were recorded. In the Cytokine study, SF was analyzed for interleukin (IL)-1-beta,IL-6, IL-8, IL-10, IL-12p70, interferon-gamma (IFN-gamma), tumor necrosis factor-alpha (TNF-alpha), IL-17, and transforming growth factor-beta (TGF-beta) by multiplexed cytokine analysis.In the Cell study, SF samples were immunophenotyped by flow cytometry, including surface markers CD4+ (CD3+), CD8+ (CD3+), and following stimulation for intracellular IFN-gamma and IL-17. The patients were divided into two groups by age median-split.Statistical analysisCategorical variables were reported as frequencies. Continuous variables were compared using Student’s t-test or in case of non-normal distribution Mann-Whitney U test.Table 1.Patients CharacteristicsMedians, (IQR), Frequenciesin %Cytokine study(n=15)Cell study(n=19)Age [years]76.6 (69.5; 83.0)59.0 (54.5; 76.0)Age Median Split7565Male80.0%68%Gout; CPPD patients [n pat]crystals*10; 510; 9Oligo-/Polyarticular [n pat]78IQR=Interquartile ranges, CPPD=Calcium pyrophosphate deposition disease, n pat=number of patientsCytokine studyMedian C-reactive (CRP), SUA levels and synovial cell counts were higher in the older patient group. Serum creatinine levels were similar between the two groups. Synovial IL-1-beta, IL-8, and IL-17 levels were significantly higher in the older subjects. Age was correlated with SF IL-1-beta (r=0.62, p=0.02), IL-17 (r=0.63, p=0.04) and IL-8 (r=0.54, p=0.04) levels.Cell study:Median CRP was higher in older patients: 87 mg/l (IQR 65; 115) vs. 20 mg/l (IQR 7; 65, p=0.0129). Although not significant, a higher frequency of total Th17 (both CD4+IL17+ and CD8+IL17+) T-cells were seen in the SF of the older patient group. The remaining T-cell subsets were comparable between the two groups.Conclusion:Gout and CPPD are paradigms for auto-inflammatory diseases. We here show an important autoinflammation enhancing cofactor: age. Inflammation measured as serum CRP, SF-IL-8, SF-IL-1-beta, and SF-IL-17 was pronounced in the older patients. Moreover, the adaptive immune system with a predominant Th-17 immune response was more prominent in the older patient group. High IL-17 concentrations may promote differentiation of T-cells in Th-17 cells and thus perpetuate inflammation in older patients with crystal arthritis (4).References:[1]Kuo C-F, Grainge MJ, Zhang W, Doherty M. Global epidemiology of gout: prevalence, incidence and risk factors. Nat Rev Rheumatol 2015;11:649-62.[2]Goronzy JJ, Weyand CM. Immune aging and autoimmunity. Cell Mol Life Sci 2012;69:1615-23.[3]Nieuwenhuis WP, Mangnus L, van Steenbergen HW, Newsum EC, Huizinga TWJ, Reijnierse M, et al. Older age is associated with more MRI-detected inflammation in hand and foot joints. Rheumatology 2016;55:2212-9.[4]Eleftheriadis T, Pissas G, Sounidaki M, Antoniadi G, Tsialtas I, Liakopoulos V, et al. Urate crystals directly activate the T-cell receptor complex and induce T-cell proliferation. Biomed Rep 2017;7:365-9.Disclosure of Interests:None declared