首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Effect of pentoxifylline in addition to losartan on proteinuria and GFR in CKD: a 12-month randomized trial.
【24h】

Effect of pentoxifylline in addition to losartan on proteinuria and GFR in CKD: a 12-month randomized trial.

机译:除氯沙坦外,己酮可可碱对CKD中蛋白尿和GFR的影响:一项为期12个月的随机试验。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Pentoxifylline potently inhibits cell proliferation, inflammation, and extracellular matrix accumulation. Human studies have proved its antiproteinuric effect in patients with glomerular diseases. Its benefit in addition to angiotensin receptor blockade in patients with chronic kidney disease is not clear. STUDY DESIGN: Randomized controlled study. SETTING & PARTICIPANTS: 85 patients with estimated glomerular filtration rate (eGFR) of 10 to 60 mL/min/1.73 m(2) and proteinuria with protein greater than 500 mg/g of creatinine on treatment with losartan, 100 mg/d, for longer than 6 months were screened in National Taiwan University Hospital. INTERVENTION: In the first stage (12 months), group 1 served as control and group 2 was administered pentoxifylline. In the second stage (6 months), both groups were administered pentoxifylline. The pentoxifylline dose was 400 mg twice daily for patients with eGFR of 30 to 60 mL/min/1.73 m(2) or once daily for patients with eGFR of 10 to 29 mL/min/1.73 m(2). OUTCOMES: Proteinuria and eGFR. MEASUREMENTS: Proteinuria was assessed as total protein-creatinine ratio, eGFR was computed by using the Modification of Diet in Renal Disease Study equation. RESULTS: 27 and 29 patients were randomly assigned to groups 1 and 2, respectively. In the first stage, pentoxifylline decreased median proteinuria from 1,140 to 800 mg/g (median change, -23.9%) compared with 1,410 to 1,810 mg/g (median change, 13.8%) in the control group. The difference between groups was 38.7% (95% confidence interval, 25.7 to 51.6; P < 0.001). The change in proteinuria was related to the change in urinary tumor necrosis factor alpha and monocyte chemoattractant protein 1 excretion (R = 0.64 and R = 0.55, respectively; P < 0.001 for both). In the second stage, pentoxifylline reproduced the change in proteinuria in group 1. LIMITATIONS: Small sample size, disease of late stages, open-labeled study. CONCLUSIONS: Pentoxifylline added to losartan therapy for 1 year decreased proteinuria in patients with CKD stages 3 to 5. A large-scale clinical trial is necessary to confirm this result.
机译:背景:己酮可可碱有效抑制细胞增殖,炎症和细胞外基质积聚。人体研究证明其在肾小球疾病患者中具有抗蛋白尿作用。除对慢性肾脏病患者的血管紧张素受体阻滞作用外,其益处尚不清楚。研究设计:随机对照研究。地点和参与者:85例肾小球滤过率(eGFR)估计为10至60 mL / min / 1.73 m(2)的患者,接受氯沙坦100 mg / d治疗时蛋白尿的肌酐大于500 mg / g的蛋白尿在台湾大学医院进行了超过6个月的筛查。干预:在第一阶段(12个月),第1组作为对照组,第2组给予己酮可可碱。在第二阶段(6个月),两组均使用己酮可可碱。己酮可可碱的剂量为eGFR为30至60 mL / min / 1.73 m(2)的患者每天两次,或eGFR为10至29 mL / min / 1.73 m(2)的患者每天两次。结果:蛋白尿和eGFR。测量:蛋白尿被评估为总蛋白-肌酐比值,eGFR通过使用肾脏疾病研究中饮食的修正公式计算。结果:分别将27和29例患者随机分为1组和2组。在第一阶段,己酮可可碱将蛋白尿中位数从1,140降低至800 mg / g(中位数变化,-23.9%),而对照组为1,410到1,810 mg / g(中位数变化,13.8%)。两组之间的差异为38.7%(95%置信区间为25.7至51.6; P <0.001)。蛋白尿的变化与尿肿瘤坏死因子α和单核细胞趋化蛋白1排泄的变化有关(分别为R = 0.64和R = 0.55;两者均P <0.001)。在第二阶段,己酮可可碱可重现第1组蛋白尿的变化。局限性:样本量小,晚期疾病,开放标签研究。结论:氯沙坦治疗中加用己酮可可碱1年,可降低CKD 3至5期患者的蛋白尿。需要进行大规模的临床试验以证实这一结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号