脂肪因子在银屑病关节炎骨质破坏中的意义
[Abstract]:Background (PsA) of psoriatic arthritis has a significant tendency to destroy bone; metabolic syndrome is very high in PsA; adipose factors (especially leptin and adiponectin) are involved in the pathogenesis of metabolic syndrome. Recent studies suggest that they also play a role in rheumatic diseases and bone metabolism. Objective to measure the concentrations of osteoclast associated cytokines: tumor necrosis factor- 伪 (TNF- 伪), nuclear factor- 魏 B receptor activator ligand (RANKL), osteoprotegerin (OPG) and fat factors: leptin, resistin, adiponectin, chemotactic factor and omental hormone. To evaluate the relationship between (OCP) level of circulating osteoclast precursor cells, imaging score and disease activity index, and to understand the significance of fat factor in bone destruction of PsA. Methods 41 patients with PsA, 20 patients with psoriasis without arthritis and 24 healthy volunteers were selected as control. PsAJAI was used to evaluate arthritis activity, modified Sharp score and Pap radiology index (BASRI) to evaluate bone erosion in PsA patients. The concentrations of TNF-a,RANKL,OPG, leptin, resistin, adiponectin, chemoattractant and omentin in plasma were determined by ELISA method. The OC count of peripheral blood mononuclear cells stimulated by RANKL and macrophage colony stimulating factor (M-CSF) was used to reflect the OCP level. The levels of cytokines and fat factors in each group and their relationship with bone erosion and disease activity index were compared. Results compared with the control group, plasma TNF- 伪, RANKL,OCP, leptin and omental hormone concentrations in PsA patients were higher, but adiponectin and chemoattractant concentrations were lower. Serum TNF- 伪, RANKL, leptin and omental hormone concentrations were positively correlated with OCP, while serum adiponectin concentrations were negatively correlated with OCP. Serum TNF- 伪, RANKL, leptin were positively correlated with PsAJAI, and TNF-a was positively correlated with imaging score. Conclusion this study showed that plasma OCP increased in patients with PsA, and there was a disturbance of cytokines and fat factors related to bone remodeling. The elevated levels of circulating leptin and omentin in patients with PsA may contribute to the occurrence of bone destruction in arthritis. The specific mechanism of fat factor in regulating PsA bone destruction needs further study. This may provide evidence for clinical treatment of PsA to find effective intervention targets.
【学位授予单位】:复旦大学
【学位级别】:博士
【学位授予年份】:2012
【分类号】:R758.63
【共引文献】
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