Badiou Stéphanie, Cristol Jean-Paul, Jaussent Isabelle, Terrier Nathalie, Morena Marion, Maurice François, Leray-Moragues Hélène, Rivory Jean-Pierre, Chalabi Lofti, Delcourt Cécile, Canaud Bernard, Dupuy Anne-Marie
Biochemistry Laboratory, Lapeyronie University Hospital, 371 Avenue Doyen Gaston Giraud, F34295 Montpellier Cedex 5, France.
Clin J Am Soc Nephrol. 2008 Mar;3(2):423-30. doi: 10.2215/CJN.02010507. Epub 2008 Jan 30.
Inflammation-induced atherosclerosis and enhanced susceptibility to infection are linked to immune dysfunction and account for an important part of mortality in hemodialysis patients. This 4-yr prospective study aimed to use cytokine proteomic determination for predicting cardiovascular and noncardiovascular mortality in hemodialysis patients.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Levels of 12 cytokines were measured using a proteomic biochip system in 134 patients who were on stable hemodialysis and compared with a control group of 150 healthy volunteers. Cox proportional hazards regression analysis was used to determine the relationship between cytokine and clinical outcome.
A proinflammatory state characterized by decreased anti-/proinflammatory cytokine ratio was evidenced in hemodialysis patients compared with control subjects. After adjustment for age, gender, smoking, and high-sensitivity C-reactive protein levels, IL-6 and (IL-4+IL-10)/IL-6 ratio were associated with a significant and specific enhanced hazard ratio of cardiovascular mortality (hazard ratio 11.32 [95% confidence interval 2.52 to 50.90; P < 0.01] and hazard ratio 3.14 [95% confidence interval 1.20 to 8.22; P < 0.05], respectively, when comparing the third and first tertiles). It is interesting that (IL-4+IL-6+IL-10)/(IL-2+IFN-gamma) ratio, used as a marker of lymphocytes T helper subsets cytokine secretion, was associated only with noncardiovascular mortality (hazard ratio 4.93; 95% confidence interval 1.03 to 23.65; P < 0.05).
Beyond the strong prediction of cardiovascular mortality by IL-6, determination of cytokine ratios can be useful to identify hemodialysis patients with increased noncardiovascular mortality risk.
炎症诱导的动脉粥样硬化以及对感染易感性的增加与免疫功能障碍相关,是血液透析患者死亡的重要原因。这项为期4年的前瞻性研究旨在通过细胞因子蛋白质组学检测来预测血液透析患者的心血管和非心血管死亡率。
设计、地点、参与者及测量方法:使用蛋白质组生物芯片系统检测了134例接受稳定血液透析患者的12种细胞因子水平,并与150名健康志愿者组成的对照组进行比较。采用Cox比例风险回归分析来确定细胞因子与临床结局之间的关系。
与对照组相比,血液透析患者呈现出以抗炎/促炎细胞因子比例降低为特征的促炎状态。在调整年龄、性别、吸烟和高敏C反应蛋白水平后,IL-6以及(IL-4 + IL-10)/IL-6比值与心血管死亡率显著且特异性地增加的风险比相关(比较第三个和第一个三分位数时,风险比分别为11.32 [95%置信区间2.52至50.90;P < 0.01]和3.14 [95%置信区间1.20至8.22;P < 0.05])。有趣的是,用作淋巴细胞辅助性T亚群细胞因子分泌标志物的(IL-4 + IL-6 + IL-10)/(IL-2 + IFN-γ)比值仅与非心血管死亡率相关(风险比4.93;95%置信区间1.03至23.65;P < 0.05)。
除了IL-6对心血管死亡率有很强的预测作用外,细胞因子比值的测定有助于识别非心血管死亡风险增加的血液透析患者。