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首页> 外文期刊>Journal of the American Society of Nephrology: JASN >Additive antiproteinuric effect of pentoxifylline in patients with type 2 diabetes under angiotensin II receptor blockade: a short-term, randomized, controlled trial.
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Additive antiproteinuric effect of pentoxifylline in patients with type 2 diabetes under angiotensin II receptor blockade: a short-term, randomized, controlled trial.

机译:己酮可可碱对2型糖尿病患者在血管紧张素II受体阻滞下的加性抗蛋白尿作用:一项短期,随机,对照试验。

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摘要

Despite the beneficial effects of blockade of the renin-angiotensin system in diabetic nephropathy (DN), albuminuria and progression of renal disease are not completely halted by these agents. Therefore, it is necessary to explore potential antiproteinuric and renoprotective effects of innovative therapeutic approaches. This study tested the hypothesis that the combination of pentoxifylline (PTF) with angiotensin II receptor blockers in normotensive patients with type 2 diabetes produces an additive antiproteinuric effect. Sixty-one patients with DN and residual albuminuria despite treatment with the recommended doses of ARB for >1 yr were randomly assigned to receive the addition of 1200 mg of PTF daily (n = 30) or to a control group (n = 31). Baseline characteristics were similar between groups, and correlation analysis showed a significant association between urinary albumin excretion (UAE) and urinary TNF-alpha (R = 0.53, P < 0.001). After 4 mo, albuminuria showed a significant decrease in patientswho received PTF, from 900 mg/24 h (466 to 1542 mg/d) to 791 mg/24 h (309 to 1400 mg/d; P < 0.001), whereas no significant changes were observed in the control group: 920 mg/24 h (450 to 1489 mg/d) at baseline, and 900 mg/24 h (428 to 1800 mg/d) at the end of the study. The mean percentage variation of UAE in the treatment and control groups was -16.7 and 5.5%, respectively (between-group comparison, P < 0.001). This additive antiproteinuric effect was not dependent on changes in BP or metabolic control. However, both serum and urinary levels of TNF-alpha also decreased in patients who received PTF, from 6.4 pg/ml (2.1 to 9.7) and 16 pg/mg (8 to 29) at baseline to 4.6 pg/ml (0.4 to 9) and 14.2 pg/mg (3 to 26) at the end of the study, respectively (P < 0.01), without significant variations in control patients. Moreover, regression analysis at the end of the study showed a correlation between the change in UAE and the change in urinary TNF-alpha in patients who were treated with PTF (R = 0.49, P < 0.001). In conclusion, administration of PTF to patients who have type 2 diabetes and are under long-term treatment with an ARB produces a significant additive antiproteinuric effect associated with a reduction of urinary TNF-alpha excretion.
机译:尽管阻断肾素-血管紧张素系统在糖尿病性肾病(DN)中具有有益作用,但这些药物并未完全阻止白蛋白尿和肾脏疾病的进展。因此,有必要探索创新治疗方法的潜在抗蛋白尿和肾保护作用。这项研究检验了以下假设,即在2型糖尿病血压正常的患者中,己酮可可碱(PTF)与血管紧张素II受体阻滞剂的组合会产生加性抗蛋白尿作用。尽管采用推荐剂量的ARB治疗超过1年,但仍有DN和残余白蛋白尿的61例患者被随机分配为每天接受1200 mg PTF(n = 30)或对照组(n = 31)。各组之间的基线特征相似,相关分析显示尿白蛋白排泄(UAE)与尿TNF-α之间存在显着相关性(R = 0.53,P <0.001)。 4个月后,接受PTF的患者的蛋白尿显着减少,从900 mg / 24 h(466至1542 mg / d)降至791 mg / 24 h(309至1400 mg / d; P <0.001)。在对照组中观察到变化:基线时为920 mg / 24 h(450至1489 mg / d),研究结束时为900 mg / 24 h(428至1800 mg / d)。治疗组和对照组中阿联酋的平均百分比变化分别为-16.7和5.5%(组间比较,P <0.001)。这种附加的抗蛋白尿作用不依赖于血压的变化或代谢控制。但是,接受PTF的患者的血清和尿液中TNF-α的水平也均从基线时的6.4 pg / ml(2.1至9.7)和16 pg / mg(8至29)降低到4.6 pg / ml(0.4至9) )和研究结束时的14.2 pg / mg(3至26)(P <0.01),对照组患者无明显差异。此外,研究结束时的回归分析显示,接受PTF治疗的患者中,UAE的变化与尿中TNF-α的变化之间存在相关性(R = 0.49,P <0.001)。总之,对患有2型糖尿病且正在接受ARB长期治疗的患者施用PTF会产生与尿TNF-α排泄减少相关的显着的加性抗蛋白尿作用。

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