Oguz F M, Oguz A, Uzunlulu M
Ic Hastaliklari Klinigi, Istanbul-Turkey.
Acta Clin Belg. 2007 Jul-Aug;62(4):218-22. doi: 10.1179/acb.2007.035.
It is well known that increased insulin resistance is associated with the development of cardiovascular disease in patients with rheumatoid arthritis and that tumour necrosis factor-alpha plays an important role in this process. Infliximab is a chimeric monoclonal anti-tumour necrosis factor-alpha antibody. This study investigates the effects of long term infliximab treatment on insulin resistance in patients with rheumatoid arthritis.
Seven rheumatoid arthritis patients (6 female and 1 male; mean age: 44.6 +/- 12.3, mean duration of disease: 6.8 y) for whom infliximab treatment had been planned at the rheumatology and internal medicine clinics were included. Patients were evaluated during and at the end of the study with a mean follow-up duration of 9.6 months. Fasting plasma glucose, fasting plasma insulin levels and serum lipid profile were assessed at baseline and throughout the treatment period (prior to every infusion). Homeostasis Model Assessment of Insulin Resistance model was used for the assessment of insulin sensitivity.
Fasting insulin and Homeostasis Mode Assessment of Insulin Resistance levels decreased after treatment (from 19.4 +/- 7.7 microU/ml to 8.9 +/- 4.1 microU/ml and from 2.4 +/- 1 to 1.1 +/- 0.5, respectively; p < 0.05 for both). No significant change was observed in other parameters.
An improvement in insulin sensitivity was observed in patients receiving long term infliximab treatment for rheumatoid arthritis.
众所周知,类风湿关节炎患者胰岛素抵抗增加与心血管疾病的发生有关,且肿瘤坏死因子-α在此过程中起重要作用。英夫利昔单抗是一种嵌合型抗肿瘤坏死因子-α单克隆抗体。本研究调查长期英夫利昔单抗治疗对类风湿关节炎患者胰岛素抵抗的影响。
纳入7例类风湿关节炎患者(6例女性,1例男性;平均年龄:44.6±12.3岁,平均病程:6.8年),这些患者在风湿病科和内科诊所计划接受英夫利昔单抗治疗。在研究期间及结束时对患者进行评估,平均随访时间为9.6个月。在基线时及整个治疗期间(每次输注前)评估空腹血糖、空腹血浆胰岛素水平和血脂谱。采用胰岛素抵抗稳态模型评估法评估胰岛素敏感性。
治疗后空腹胰岛素水平和胰岛素抵抗稳态模型评估值下降(分别从19.4±7.7微单位/毫升降至8.9±4.1微单位/毫升,从2.4±1降至1.1±0.5;两者p均<0.05)。其他参数未观察到显著变化。
接受长期英夫利昔单抗治疗的类风湿关节炎患者胰岛素敏感性得到改善。