Rheumatology Division, Hospital Xeral-Calde, Lugo, Spain.
Ann N Y Acad Sci. 2010 Apr;1193:153-9. doi: 10.1111/j.1749-6632.2009.05287.x.
Increased prevalence of insulin resistance has been observed in patients with rheumatoid arthritis (RA). High-grade systemic inflammation is implicated in the development of insulin resistance in these patients. Tumor necrosis factor (TNF)-alpha is a potent proinflammatory cytokine that plays a role in the initiation and progression of inflammation and the mechanisms associated with accelerated atherosclerosis in RA. In assessing data immediately prior to and after intravenous infusion of the anti-TNF-alpha monoclonal antibody-infliximab in RA patients on period treatment with this drug attributable to disease refractory to conventional disease-modifying antirheumatic drugs, a dramatic improvement of insulin resistance and insulin sensitivity was observed. A long-term positive effect of TNF-alpha antagonists infliximab and etanercept on insulin resistance in RA patients with severe disease was also reported. These results highlight the importance of therapies that act blocking TNF-alpha function to reduce the mechanisms implicated in the development of the metabolic syndrome observed in RA.
在类风湿关节炎(RA)患者中,观察到胰岛素抵抗的患病率增加。在这些患者中,高级别的全身炎症与胰岛素抵抗的发展有关。肿瘤坏死因子(TNF)-α是一种有效的促炎细胞因子,在炎症的发生和发展以及与 RA 中加速动脉粥样硬化相关的机制中发挥作用。在评估 RA 患者在静脉输注抗 TNF-α单克隆抗体 infliximab 之前和之后的数据时,这些患者正在接受该药的周期性治疗,归因于对常规疾病修饰抗风湿药物难治的疾病,观察到胰岛素抵抗和胰岛素敏感性显著改善。还报告了 TNF-α拮抗剂 infliximab 和 etanercept 对严重 RA 患者胰岛素抵抗的长期积极影响。这些结果强调了作用于阻断 TNF-α功能的治疗方法的重要性,以减少 RA 中观察到的代谢综合征发展中涉及的机制。