Adiponectin is a mediator of the inverse association of adiposity with radiographic damage in rheumatoid arthritis.

Jon T Giles, Matthew Allison, Clifton O Bingham, William M Scott, Joan M Bathon
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引用次数: 125

Abstract

Objective: Recent reports have suggested that increasing adiposity may protect against radiographic damage in rheumatoid arthritis (RA). We explored the role of serum adipokines (adiponectin, resistin, and leptin) in mediating this association.

Methods: Patients with RA underwent total-body dual x-ray absorptiometry for measurement of total and regional body fat and lean mass, abdominal computed tomography for measurement of visceral fat area, and radiographs of the hands and feet scored according to the modified Sharp/van der Heijde (SHS) method. Serum levels of adipokines were measured and cross-sectional associations with radiographic damage were explored, adjusting for pertinent confounders. The associations of measures of adiposity with radiographic damage were explored with the introduction of adipokines into multivariable modeling as potential mediators.

Results: Among the 197 patients studied, adiponectin demonstrated a strong association with radiographic damage, with the log SHS score increasing by 0.40 units for each log unit increase in adiponectin (P = 0.001) after adjusting for pertinent predictors of radiographic damage. Adiponectin independently accounted for 6.1% of the explainable variability in SHS score, a proportion comparable with rheumatoid factor, and greater than HLA-DRB1 shared epitope alleles or C-reactive protein levels. Resistin and leptin were not associated with radiographic damage in adjusted models. An inverse association between visceral fat area and radiographic damage was attenuated when adiponectin was modeled as a mediator. The association of adiponectin with radiographic damage was stronger in patients with longer disease duration.

Conclusion: Adiponectin may represent a mechanistic link between low adiposity and increased radiographic damage in RA. Adiponectin modulation may represent a novel strategy for attenuating articular damage.

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脂联素是类风湿性关节炎中肥胖与影像学损害负相关的中介。
目的:最近的报道表明,增加脂肪可以防止类风湿关节炎(RA)的影像学损害。我们探讨了血清脂肪因子(脂联素、抵抗素和瘦素)在介导这种关联中的作用。方法:RA患者采用全身双x线吸收仪测量全身和局部体脂和瘦质量,腹部计算机断层扫描测量内脏脂肪面积,手脚x线片根据改进的Sharp/van der Heijde (SHS)方法评分。测量血清脂肪因子水平,探讨与放射学损伤的横断面关联,调整相关混杂因素。通过将脂肪因子引入多变量模型作为潜在的介质,探讨了肥胖测量与影像学损伤之间的关联。结果:在研究的197例患者中,脂联素显示出与影像学损伤的强相关性,在调整影像学损伤的相关预测因子后,脂联素每增加log单位,其log SHS评分增加0.40个单位(P = 0.001)。脂联素单独占SHS评分可解释变异性的6.1%,这一比例与类风湿因子相当,并且大于HLA-DRB1共享表位等位基因或c反应蛋白水平。在调整后的模型中,抵抗素和瘦素与影像学损伤无关。当脂联素被建模为介质时,内脏脂肪面积和放射损伤之间的负相关被减弱。在病程较长的患者中,脂联素与影像学损害的相关性更强。结论:脂联素可能是类风湿性关节炎患者低脂肪和放射学损伤增加之间的机制联系。脂联素调节可能是一种减轻关节损伤的新策略。
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Arthritis and rheumatism
Arthritis and rheumatism 医学-风湿病学
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