抗TNF α (certolizumab)治疗对轴型脊柱炎(强直性脊柱炎)患者胰岛素抵抗、脂质参数及心血管风险的影响

Hasan Göğebakan, G. Yıldırım Çetin
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引用次数: 0

摘要

目的:评估certolizumab治疗对强直性脊柱炎(AS)患者胰岛素抵抗(IR)、脂质参数和心血管(CV)风险的影响。方法:本前瞻性研究纳入80例AS患者(男性52例,女性28例)和74例对照组(男性48例,女性26例)。比较AS患者与对照组的基础值。所有伴有活动性疾病的AS患者均接受certolizumab治疗。在certolizumab治疗前和24周后获得生化谱。用稳态模型评估-胰岛素抵抗(HOMA-IR)测量IR,用定量胰岛素敏感性控制指数(QUICKI)测量胰岛素敏感性。采用Framingham方程评价心血管危险因素。结果:在certolizumab治疗24周后,总胆固醇(TC)、高密度脂蛋白胆固醇(HDL-C)和甘油三酯(TG)值有统计学意义的增加。血浆动脉粥样硬化指数(PAI)和低密度脂蛋白胆固醇(LDL-C)值无统计学意义变化。HOMA-IR有统计学意义上的显著降低,QUICKI有统计学意义上的增加。当Framingham风险评分与基线值比较时,在第24周发现风险有统计学意义上的显著降低。结论:Certolizumab治疗与HDL-C、TC和TG水平的显著升高相关,而PAI和LDL-C没有显著变化,并被确定为增加胰岛素敏感性和降低胰岛素抵抗。在certolizumab治疗开始后24周,收缩压和10年Framingham风险评分也有显著降低。
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The effect of anti TNF alpha (certolizumab) treatment on insulin resistance, lipid parameters and cardiovascular risk in patients with axial spondyloarthritis (ankylosing spondylitis)
Objectives: To evaluate the effects of certolizumab treatment on insulin resistance (IR), lipid parameters, and cardiovascular (CV) risk in patients with ankylosing spondylitis (AS). Methods: This prospective study included 80 consecutive patients with AS (52 males, 28 females) and 74 control subjects (48 males, 26 feemales). The AS patients and control group were compared in respect of basal values. All AS patients with active disease were treated with certolizumab. Biochemical profiles were obtained before and after 24 weeks of certolizumab treatment. Homeostatic model assessment-insulin resistance (HOMA-IR) was used to measure IR and the quantitative insulin sensitivity control index (QUICKI) was used to measure insulin sensitivity. The Framingham equation was used to evaluate CV risk factors. Results: A statistically significant increase was determined in total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and triglyceride (TG) values after 24 weeks of certolizumab treatment. No statistically significant change was determined in the plasma atherogenic index (PAI) and low-density lipoprotein cholesterol (LDL-C) values. A statistically significant decrease was determined in HOMA-IR and an increase in QUICKI. When the Framingham risk scoring was compared with the baseline values, a statistically significant decrease in risk was found at week 24. Conclusions: Certolizumab therapy was associated with a significant increase in HDL-C, TC, and TG levels without any significant change in PAI and LDL-C, and was determined to increase insulin sensitivity and lower insulin resistance. There was also a significant reduction in SBP and 10-year Framingham risk scores at 24 weeks after the start of certolizumab therapy.
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