首页> 外文期刊>Atherosclerosis >Effects of darbepoetin-alpha on plasma pro-inflammatory cytokines, anti-inflammatory cytokine interleukin-10 and soluble Fas/Fas ligand system in anemic patients with chronic heart failure.
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Effects of darbepoetin-alpha on plasma pro-inflammatory cytokines, anti-inflammatory cytokine interleukin-10 and soluble Fas/Fas ligand system in anemic patients with chronic heart failure.

机译:darbepoetin-α对慢性心力衰竭贫血患者血浆促炎细胞因子,抗炎细胞因子白细胞介素10和可溶性Fas / Fas配体系统的影响。

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Pro-inflammatory cytokine over-expression may be implicated to the pathogenesis of anemia in chronic heart failure (CHF) through the suppression of bone marrow erythropoiesis. Erythropoietin administration has anti-inflammatory and anti-apoptotic properties in experimental CHF models and improves exercise capacity in anemic CHF patients. The present study investigates the effects of recombinant human erythropoietin analogue darbepoetin-alpha on circulating pro-inflammatory cytokines and soluble Fas/soluble Fas ligand system in patients with CHF and anemia. Forty-one CHF patients (NYHA class: II-III; left ventricular (LV) ejection fraction (EF) 40%; hemoglobin 12.5g/dl; serum creatinine 2.5mg/dl) were randomized to receive either 3-month darbepoietin-* at 1.5 microg/kg every 20 days plus iron orally (n=21) or placebo plus iron orally (n=20). LV systolic function, plasma B-type natriuretic peptide (BNP), inflammatory markers (TNF-*, IL-6, CRP), anti-inflammatory cytokine IL-10, endothelial adhesion molecules (soluble ICAM-1 and VCAM-1) and soluble apoptosis mediators (soluble Fas, soluble Fas ligand), and 6-min walking distance were assessed at baseline and 3 months post-treatment. In darbepoetin-* treated patients, plasma BNP (451 (62-2770) from 802 (476-4440) pg/ml, p=0.002), IL-6 (6.5+/-4.7 from 10.5+/-7.8 pg/ml, p=0.013) and soluble Fas ligand (53.2+/-16.6 from 59.2+/-17.9 pg/ml, p=0.023) decreased significantly, while LVEF (32+/-6 from 26+/-6%, p0.001), hemoglobin (12.8+/-1.4 from 10.9+/-1.0 g/dl, p0.001) and 6-min walked distance (274+/-97 from 201+/-113m, p0.01) increased significantly. No significant changes were observed in the placebo arm, except for a worsening in 6-min walked distance (p=0.044). In conclusion, darbepoetin-alpha reduces circulating pro-inflammatory cytokine IL-6 and apoptotic mediator soluble Fas ligand in CHF patients with anemia, with a parallel improvement of cardiac performance and exercise capacity.
机译:通过抑制骨髓的红细胞生成,促炎性细胞因子的过度表达可能与慢性心力衰竭(CHF)贫血的发病机制有关。促红细胞生成素的给药在实验性CHF模型中具有抗炎和抗凋亡特性,并改善贫血CHF患者的运动能力。本研究调查了重组人促红细胞生成素类似物darbepoetin-α对CHF和贫血患者循环促炎细胞因子和可溶性Fas /可溶性Fas配体系统的影响。随机将41名CHF患者(NYHA II-III级;左心室射血分数(EF)<40%;血红蛋白<12.5g / dl;血清肌酐<2.5mg / dl)随机分3个月接受darbepoietin- *每20天以1.5 microg / kg的剂量加铁口服(n = 21)或安慰剂加铁口服(n = 20)。左室收缩功能,血浆B型利钠肽(BNP),炎性标志物(TNF-*,IL-6,CRP),抗炎细胞因子IL-10,内皮粘附分子(可溶性ICAM-1和VCAM-1)和在基线和治疗后3个月评估了可溶性细胞凋亡介体(可溶性Fas,可溶性Fas配体)和6分钟步行距离。在darbepoetin- *治疗的患者中,血浆BNP(451(62-2770)从802(476-4440)pg / ml,p = 0.002),IL-6(6.5 +/- 4.7从10.5 +/- 7.8 pg / ml ,p = 0.013)和可溶性Fas配体(从59.2 +/- 17.9 pg / ml的53.2 +/- 16.6,p = 0.023)显着降低,而LVEF(从26 +/- 6%的32 +/- 6,p < 0.001),血红蛋白(10.9 +/- 1.0 g / dl为12.8 +/- 1.4,p <0.001)和6分钟步行距离(201 +/- 113m为274 +/- 97,p <0.01)显着增加。安慰剂组没有观察到显着变化,除了步行6分钟的距离恶化(p = 0.044)。总之,darbepoetin-α可以降低CHF贫血患者的循环促炎细胞因子IL-6和凋亡介导的可溶性Fas配体,并同时改善心脏性能和运动能力。

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