首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Impact of ace inhibitors and aii receptor blockers on peritoneal membrane transport characteristics in long-term peritoneal dialysis patients.
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Impact of ace inhibitors and aii receptor blockers on peritoneal membrane transport characteristics in long-term peritoneal dialysis patients.

机译:ace抑制剂和aii受体阻滞剂对长期腹膜透析患者腹膜转运特性的影响。

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BACKGROUND: Long-term peritoneal dialysis (PD) may lead to peritoneal fibrosis and ultrafiltration failure. The latter occurs due to high solute transport rates and diabetiform peritoneal sclerosis. Angiotensin-II (AII) is known to be a growth factor in the development of fibrosis and a number of animal studies have shown it likely that inhibiting the effects of AII by angiotensin-converting enzyme (ACE) or angiotensin receptor blocker (ARB) will attenuate these complications. OBJECTIVE: To investigate the effects of ACE/AII inhibitors in long-term PD patients. Patients and SETTING: We analyzed data from 66 patients treated with PD therapy at our center for at least 2 years, during which time at least 2 standard peritoneal permeability analyses (SPAs) were performed. 36 patients were treated with ACE/AII inhibitors (ACE/ARB group); the other 30 received none of the above drugs during the entire follow-up (control group). The two groups were compared with respect to changes in peritoneal transport over the follow-up time. RESULTS: A significant difference in time course of peritoneal transport was found between the 2 groups: in the ACE/ARB group, small solute transport had decreased, while it had increased in the control group. This finding was confirmed by analysis using mixed model for repeated measures. The value of mass transfer area coefficient of creatinine was influenced by the duration of PD therapy (p = 0.017) and this interaction was different with respect to use of ACE/AII inhibitors (p = 0.037). The trend was not found in protein clearances or fluid kinetics. CONCLUSION: Our findings suggest that ACE/AII inhibition is likely to prevent the increase in mass transfer area coefficients that occurs in long-term PD, which is in line with results of experimental animal studies.
机译:背景:长期腹膜透析(PD)可能导致腹膜纤维化和超滤失败。后者的发生是由于高溶质转运速率和糖尿病样腹膜硬化。已知血管紧张素II(AII)是纤维化发展中的生长因子,许多动物研究表明,通过血管紧张素转化酶(ACE)或血管紧张素受体阻滞剂(ARB)抑制AII的作用可能会减轻这些并发症。目的:探讨ACE / AII抑制剂在长期PD患者中的作用。患者和背景:我们分析了来自我们中心接受PD治疗至少2年的66位患者的数据,在此期间,至少进行了2次标准腹膜通透性分析(SPAs)。 36例接受ACE / AII抑制剂治疗(ACE / ARB组);在整个随访过程中,其他30例均未接受上述药物治疗(对照组)。比较两组在随访时间内腹膜运输的变化。结果:两组之间的腹膜运输时间进程存在显着差异:在ACE / ARB组中,小溶质运输减少了,而在对照组中有所增加。通过使用混合模型进行重复测量的分析证实了这一发现。肌酐的传质面积系数的值受PD治疗持续时间的影响(p = 0.017),这种相互作用在使用ACE / AII抑制剂方面有所不同(p = 0.037)。在蛋白质清除率或流体动力学中未发现该趋势。结论:我们的研究结果表明,ACE / AII抑制很可能阻止长期PD中传质面积系数的增加,这与动物实验研究的结果一致。

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