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Factors correlated with improvement of endothelial dysfunction during rituximab therapy in patients with rheumatoid arthritis

机译:类风湿关节炎患者在利妥昔单抗治疗期间改善内皮功能障碍的相关因素

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Increased cardiovascular mortality has been associated with rheumatoid arthritis (RA). There are reports indicating that tumor necrosis factor (TNF) blockers may exert favorable but transient effects on the lipid profile, flow-mediated vasodilatation (FMD) of the brachial artery, and the common carotid intima–media thickness (ccIMT) in RA. We evaluated 38 RA patients (33 females and five males with a mean age of 66.7 ± 10.2 years) who were unresponsive to TNF blockers. The patients received one or more courses of two rituximab (RTX) 1000 mg infusions. Disease activity was evaluated at each visit. Investigations included erythrocyte sedimentation rate, C-reactive protein (CRP) levels, the 28-joint disease activity score (DAS28), DAS28CRP, the Health Assessment Questionnaire, the FMD percent change from baseline (FMD%), and the postnitroglycerine endothelium-independent vasodilatation. In comparison with the baseline, there was a significant improvement in clinical variables and acute-phase reactants 24 months after the start of RTX therapy. There was also a major improvement in FMD% (from baseline 5.24 ± 1.12 to 5.43 ± 1.16; P = -0.03) and a smaller change in the ccIMT (from baseline 0.69 ± 0.16 to 0.67 ± 0.12 mm P = 0.25). Univariate analysis showed that global health ( P < 0.034) was associated with the improvement in FMD%. Multivariate models showed that GH (odds ratio [OR] 0.91; 95% CI: 0.99–0.83; P = 0.032), CD19+ cells (OR 1.024; 95% CI: 1.045–1.003; P = 0.025), IgM (OR 1.025; 95% CI: 1.045–1.004; P = 0.016), and interleukin (IL)-8 (OR 0.487; 95% CI: 0.899–0.264; P = 0.021) were statistically associated with the improvement of FMD%, and that IL-8 (OR 0.717; 95% CI: 0.926–0.555; P = 0.018) was also statistically associated with improvement of ccIMT. The findings of the study confirm that RTX reduces the progression of accelerated atherosclerosis in patients with RA. They also show that improvement in CD19+ cells, IgM and GH after treatment are statistically associated with the improvement of FMD%, and that improvement in IL-8 levels after treatment is statistically associated with improved FMD% and with decrease in the ccIMT.
机译:心血管疾病死亡率增加与类风湿关节炎(RA)有关。有报道表明,肿瘤坏死因子(TNF)阻滞剂可能对RA中的脂质分布,肱动脉血流介导的血管舒张(FMD)和颈总内膜中层厚度(ccIMT)产生有利而短暂的影响。我们评估了对TNF阻滞剂无反应的38例RA患者(33例女性和5例男性,平均年龄为66.7±10.2岁)。患者接受一或多个疗程的两次利妥昔单抗(RTX)1000 mg输注。在每次访问时评估疾病活动。研究包括红细胞沉降率,C反应蛋白(CRP)水平,28关节疾病活动评分(DAS28),DAS28CRP,健康评估问卷,FMD与基线相比的变化百分比(FMD%)以及不依赖硝酸甘油的内皮细胞血管舒张。与基线相比,RTX治疗开始后24个月,临床变量和急性期反应物显着改善。 FMD%也有重大改善(从基线5.24±1.12到5.43±1.16; P = -0.03),而ccIMT的变化较小(从基线0.69±0.16到0.67±0.12 mm P = 0.25)。单因素分析表明,整体健康状况(P <0.034)与FMD%的改善有关。多变量模型显示GH(赔率[OR] 0.91; 95%CI:0.99–0.83; P = 0.032),CD19 +细胞(OR 1.024; 95%CI:1.045–1.003; P = 0.025),IgM(OR 1.025; 95%CI:1.045–1.004; P = 0.016)和白介素(IL)-8(OR 0.487; 95%CI:0.899–0.264; P = 0.021)与FMD%的改善在统计学上相关,而IL- 8(OR 0.717; 95%CI:0.926-0.555; P = 0.018)也与ccIMT的改善有统计学联系。该研究结果证实,RTX可以降低RA患者的动脉粥样硬化加速发展。他们还显示,治疗后CD19 +细胞,IgM和GH的改善与FMD%的改善有统计学联系,而治疗后IL-8水平的改善与FMD%的改善和ccIMT的减少有统计学联系。

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