The aim of our study was to evaluate the association between circulating levels of serum amyloid A protein (SAA) and disease activity in patients with juvenile idiopathic arthritis (JIA). Our study group included 41 JIA patients (9 male, 32 female), classified according to the International League of Associations for Rheumatology (ILAR) criteria (5); 16 had polyarticular onset disease and 25 had oligoarticular onset disease. Among 25 patients with oligoarticular disease, three had extended oligoarthritis. Serum amyloid A (SAA), erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were measured in both patients and 26 healthy controls. SAA levels were higher in JIA patients versus healthy controls (p<0.001). Significant positive correlations were found between SAA and the presence of active joints (rho=0.363, p<0.05), the number of active joints (rho=0.418, p<0.05), ESR (R=0.702, p<0.05) and CRP (R=0.827, p<0.05). No significant correlations between ESR and the presence of active joints (rho=0.221, p=0.225) or between ESR and the number of active joints (rho=0.118, p=0.520) were demonstrated in JIA patients. No significant correlations were obtained between CRP and the presence of active joints (rho=0.034, p=0.855) or between CRP and the number of active joints (rho=0.033, p=0.859). We discovered a significant increase in SAA levels in JIA patients, compared to controls, and a strong positive correlation between SAA level and JIA disease activity. We also discerned SAA to be a more sensitive laboratory marker than ESR and CRP for evaluating the presence and number of active joints. We suggest that SAA can be used as an additional indicator of disease activity in JIA.
Arthritis, Juvenile* ; Biomarkers ; Blood Sedimentation ; C-Reactive Protein ; Humans ; Joints ; Male ; Rheumatology ; Serum Amyloid A Protein*

Objective: Objective of this review is to summarize the currently available information on possible chondroprotective effects of mineral waters or mineral components on chondrocyte or cartilage cultures. Methodology: We conducted a search of the literature by PubMed and Scopus (the period examined was 1980-2013) using the terms “chondrocyte” and/or “cartilage” in combination with ”mineral water”, “hydrogen sulphide”, “sulphur hydrogen”. Results: A chondroprotective role of mineral water or mineral components was demonstrated by some pilot studies in chondrocyte cultures. Burguera1) studied the activity of hydrogen sulphide (H2S) in human osteoarthritic (OA) chondrocytes stimulated with Interleukin (IL)-1β. They analyzed the effects of different concentrations of a fast (NaHS) or a slow (GYY4137) release H2S donor demonstrating a significant reduction of Nitric Oxide (NO), Prostaglandin(PG)-E2, and Reactive Oxygen Species (ROS) levels in culture medium and of inducible Nitric Oxide Synthase (iNOS) gene expression, induced by IL-1β. These data were confirmed by Li2) in normal human chondrocytes stimulated by Lipopolysaccharide(LPS). GYY4137 decreased LPS-induced production of NO, PGE2, Tumor Necrosis Factor (TNF)-α and IL-6, reduced the levels and catalytic activity of iNOS and of Cyclooxygenase-2 (COX-2) and reduced LPS-induced NF-kB activation. Furthermore GYY4137 showed a strong inhibition on oxidative stress-induced cell death3). The incubation of chondrocytes cell line C-28/I2 with another H2S donor, Natrium Hydrogen Sulphide (NaHS), proved that constitutive as well as IL-1β-induced IL-6 and IL-8 expression was partially and transiently blocked by the NaHS4). Fioravanti studied the chondroprotective role of highly mineralized water, strongly acidic sulfate, rich in calcium, magnesium and iron [Vetriolo’s thermal water (VW)] in human OA chondrocytes cultivated with or without IL-1β5). For this purpose chondrocytes were cultivated in Deionized Water (DW) (DW-DMEM, controls), or in one of three different VW-DMEM media, in which DW had been totally (100%) or in part (50% or 25%) substituted with VW. The results showed that VW alone at 25% or 50% concentration did not affect the viability of cultured chondrocytes, and determined a significant survival recovery rate in cultures stimulated with IL-1β. NO levels were low both in DW-DMEM cultures and in those reconstituted with 25% or 50% of VW, and were significantly increased by IL-1β. VW at 25% or 50% concentration significantly reduced the NO production induced by IL-1β. The data of NO levels were confirmed by the immunocytochemistry assay for iNOS. Furthermore, the authors demonstrated a protective effect of VW at 25% or 50% concentration on IL-1β-induced apoptosis. Conclusions: Presented data are stimulating, but we don’t ignore the existence of a complex series of problems and limitations. One of the critical points is the controversial problem of the absorption of the minerals dissolved in mineral waters, furthermore, extrapolation of in vitro results to in vivo should be undertaken with caution.   Further studies are needed in vitro to confirm these preliminary findings.

Objective: To assess both the short-term and the long-term effectiveness of spa therapy in patients with primary knee osteoarthritis (OA) in a prospective, randomized, single blind, controlled trial. Materials and Methods: 103 outpatients with OA of the knee according to the ACR criteria (1) were enrolled. Patients were randomized 1 : 1 and allocated into two groups: 53 patients (Group A) received in addition to usual treatment (exercise, NSAIDs and/or analgesics, established SYSADOAs) a combination of daily local mud-packs applied on both knees for 20 min at an initial temperature of 45°C and bicarbonate-sulphate-calcic mineral bath water at 38°C for 15 min, from the spa centre of Chianciano Terme (Siena, Italy) for 12 applications carried out over a period of 2 weeks. 50 patients (Group B, controls) continued routine ambulatory care. Clinical assessments were performed at basal time after 2 weeks, after 3, 6, 9 and 12 months - end of the study. The primary outcome criteria were the change from baseline to month 12 in WOMAC - Total Pain Score (W-TPS) (range 0-20)* and in WOMAC - Total Physical Function Score (W-TPFS) (range 0-68)* scored by a 5-point Likert scale. A set of secondary outcomes was also assessed such as WOMAC Total Stiffness Score (W-TSS), Physical Component Summary (PCS) and Mental Component Summary (MCS) of SF-12 (ranges 0-100) and consumption of analgesic medications (paracetamol and/or NSAIDs). Results: Ten patients (9.5%) withdrew from the study: 2 in the spa-group and 8 (16%) in the control group. The assessment of pain showed a very significant improvement (p<0.001) in patients treated with mud-packs until 6 months and a less significant reduction (p<0.05) after 9 and 12 months. The control group showed a significant improvement after 2 weeks and 3 months, however this improvement is less expressed than in group A.   The differences between the two groups were significant already from 2 weeks and lasted during the follow-up.   A similar trend was observed for the WOMAC - Physical Function in the group A, group B showed a significant worsening after 6 months persisting throughout the follow-up.   The results obtained from the quality of life, SF-12 survey showed a significant improvement (p<0.001) in Physical Component, persisting throughout the follow-up period in group A. No significant modifications were found in group B during the study period.   On the contrary, significant improvement of the Mental Component Summary of SF-12 was shown at the end of the therapy in group A, but no significant differences were observed in the other time of the follow-up.   These effect on pain and function were also confirmed by the observed reduction of symptomatic drugs consumption. Tolerability of spa therapy seemed to be good, with light and transitory side effects. Conclusions: In conclusion our results, in keeping with other studies (2, 3) confirm that the beneficial effects of mud-bath therapy in patients with knee OA last over time, with significant reduction on the painful symptomatology and a significant improvement on functional capacities and on quality of life. Spa therapy can represent a useful backup to pharmacological treatment of knee OA or a valid alternative for patients who do not tolerate pharmacological treatments.