FRI0544 Urinary 6-sulfatoxymelatonin excretion and galectin-3 plasma level in patients with osteoarthritis. (12th June 2018)

• Record Type: Journal Article
• Authors: Zaichko, K.; Gumeniuk, O.; Stanislavchuk, M.
• Is Part Of: Annals of the rheumatic diseases. Volume 77(2018)Supplement 2
• Page Start: 797
• Page End: 797
• Publication Date: 2018-06-12
• Subjects: Rheumatism -- Periodicals; 616.723005
• DOI: 10.1136/annrheumdis-2018-eular.3778
• Languages: English
• ISSNs: 0003-4967

Abstract

Abstract : Background: Melatonin and galectin-3 are considered as factors in the development of immune-inflammatory and destructive changes in joints. 1–5 Melatonin has chondrogenic and antinociceptive properties, 2; 4 while galectin-3 plays an important role in cell-cell adhesion, macrophage activation, angiogenesis, and apoptosis. 1; 3 The clinical and pathogenetic significance of melatonin and galectin-3 in osteoarthritis remains on the discussion. Objectives: To study the excretion of 6-sulfatexymelatonin (metabolite of melatonin) and galectin-3 level in the blood and evaluate their association with the clinical manifestation and life quality in patients with OA. Methods: Study involved 141 patients with OA of knee joints (76.6% women), aged 58.4±7.91 years, duration of the disease 10.5±6.50 years (M±SD). 47 (33.3%) patients had knee and hip OA, 38 (27%) patients had reactive synovitis. The control group was presented by 36 practically healthy subjects (72.2% female) aged 57.1±9.95 years (M±SD). 6-sulfatoxymelatonin (6-SMT) in urine and galectin-3 in blood were determined by ELISA. The severity of pain, stiffness, and physical functioning of the joints were evaluated by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Quality of life was evaluated by Short Form-36 (SF 36). Results: It was established in patients with OA a decrease in 6-SMT excretion, (mean 25.3 vs 38.8 ng/mg creatinine in control, p<0.001). 6-SMT excretion correlated with age (r=−0.40; p<0.001) and was more significant in patients with knee +hip OA (mean 26.5 vs 23.0 ng/mg creatinine in patients with OA of the knee only, p<0.001). Lower levels of 6-SMT excretion associated with higher pain and with lower quality of life. Patients with OA had increased galectin-3 levels in the blood (mean 16.4 vs 10.1 ng/ml in the control, p<0.001. In patients with OA of knee and hip joints were estimated higher levels of galectin-3. Levels of galectin-3 were significantly higher in patients with synovitis (mean 21.5 vs. 13.8 ng/ml without synovitis, p<0.001). The increase of galectin-3 in the blood was associated with a marked increase of the total WOMAC index and with decrease of life quality. The level of galectin-3 directly correlated with age, disease duration (r=0.28, 0.23, p<0.01) and inversely correlated with 6-SMT excretion (r=−0.28; p<0.01). Conclusions: Lower levels of melatonin and higher of galectin-3 were associated with higher WOMAC index and poorer quality of life in patients with OA. This association may reflect possible pathogenic role of melatonin and galectin-3 in OA. References: [1] Forsman H, Islander U, Andréasson E, et al. Galectin 3 aggravates joint inflammation and destruction in antigen-induced arthritis. Arthritis Rheum2011;63(2):445–454. [2] Hong Y, Kim H, Lee S, Jin Y, et al. Role of melatonin combined with exercise as a switch-like regulator for circadian behavior in advanced osteoarthritic knee. Oncotarget2017;8(57):97633–97647. [3] Hu Y, Yéléhé-Okouma M, Ea HK, et al. Galectin-3: A key player in arthritis. Joint Bone Spine2017;84(1):15–20. [4] Pei M, He F, Wei L, Rawson A. Melatonin enhances cartilage matrix synthesis by porcine articular chondrocytesJ. Pineal. Res. 2009;46(2):181–187. Disclosure of Interest: None declared