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The role of ferritin and adiponectin as predictors of cartilage damage assessed by arthroscopy in patients with symptomatic knee osteoarthritis

医学 骨关节炎 脂联素 内科学 铁蛋白 滑液 软骨 关节软骨损伤 内分泌学 软骨损伤 胃肠病学 碱性磷酸酶 维生素D与神经学 关节镜检查 软骨寡聚基质蛋白 病理 外科 肥胖 关节软骨 胰岛素抵抗 解剖 替代医学 化学 生物化学
作者
Nugzar Oren,Gisele Zandman‐Goddard,Hadar Oz,Dror Lakstein,Zeev Feldbrin,Marina Shargorodsky
出处
期刊:Best Practice & Research: Clinical Rheumatology [Elsevier]
卷期号:32 (5): 662-668 被引量:26
标识
DOI:10.1016/j.berh.2019.04.004
摘要

The aim of the present study was to evaluate whether circulating serum ferritin and adiponectin (ADP) in the serum and synovial fluid correlate with cartilage damage severity assessed by arthroscopy in patients with knee osteoarthritis. The 40 subjects with symptomatic knee osteoarthritis were divided into four groups according to arthroscopy assessed cartilage damage, using Outerbridge (OB) grading. Group I included minor damage while Group IV included severe damage. Metabolic parameters, bone homeostasis, and insulin resistance markers were determined. Synovial fluid of the affected knee joint was obtained and assessed for synovial adiponectin levels. Parameters of bone homeostasis in the serum including levels of PTH, alkaline phosphatase, 25OH vitamin D, serum calcium and phosphorus were similar in the four groups. A significant difference in the level of serum ferritin was found: ferritin levels increased from Group 1 to Group 4 in a continuous fashion (p < 0.035). In General linear model (GLM) analysis significant by-group differences in circulating ferritin persisted even after adjustment (p = 0.030). Although all groups were similar in terms of serum ADP levels, between groups difference in synovial fluid ADP was found (p < 0.037). However, after controlling for the age, there was no between-group difference in terms of synovial ADP levels. Serum ferritin levels were associated with cartilage damage severity assessed by arthroscopy. This association was independent of age, sex, BMI, and CRP levels suggesting that ferritin may be actively involved in the progression of cartilage damage in patients with symptomatic knee OA.
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