大剂量血管紧张素受体阻滞剂治疗高血压合并慢性肾病患者的长期安全性

Adam J Weinberg, Dion H Zappe, Rajeev Ramadugu, Marc S Weinberg
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引用次数: 13

摘要

背景:减少肾脏疾病患者尿蛋白排泄是预防肾脏和心血管疾病进展的重要治疗靶点。血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂(ARBs)等药物可以阻断肾素-血管紧张素-醛固酮系统的作用,因为它们可以降低血压和蛋白尿。最近,使用更高剂量的arb,达到最大批准剂量的三倍,导致蛋白质排泄进一步减少。尽管这种治疗方法有效,但尚未对接受高剂量ARB治疗的患者进行长期安全性分析。目的:探讨大剂量ARB治疗的长期安全性。方法:观察48例患者[男44例,女4例;年龄64 +/- 15岁(平均+/- SD),体重88 +/- 28 kg,估计肾小球滤过率53 +/- 23 ml/min],接受高剂量(比最大批准剂量大1.5-5倍)arb治疗,持续40 +/- 24个月(范围6-98个月)。结果:ARB的平均剂量有随时间增加的趋势,在研究结束时是研究开始时的3.2 +/- 1.2倍。收缩压在研究期开始和结束时相似(分别为132 +/- 20和125 +/- 20 mmHg),但舒张压在整个研究过程中显示下降,与基线(78 +/- 11 mmHg)相比,与最大ARB剂量(73 +/- 11和72 +/- 10 mmHg)的1.5倍和2倍相关(P < 0.05)。血清钾(0.2 +/- 0.9 mmol/l)和肌酐(0.3 +/- 0.7 mg/dl)浓度随剂量的增加从基线到研究结束有增加的趋势(P > 0.05)。血清肌酐浓度在最大剂量的3倍和4倍时更高(P < 0.05),但分别仅比基线增加12%和20%。结论:慢性肾脏疾病患者的大剂量ARB治疗与血清肌酐或钾的任何临床显着的长期负面影响无关,因此是进一步减少尿蛋白排泄的重要治疗方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term safety of high-dose angiotensin receptor blocker therapy in hypertensive patients with chronic kidney disease.

Background: Reducing urinary protein excretion in patients with renal disease is an important therapeutic target to prevent the progression of renal and cardiovascular disease. Drugs such as angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (ARBs), which block the actions of the renin-angiotensin-aldosterone system, are recommended because they reduce blood pressure and proteinuria. Recently, the use of higher doses of ARBs, up to three times the maximal approved dose, resulted in further reductions in protein excretion. Despite the effectiveness of this therapeutic approach, no long-term safety analysis has been conducted in patients receiving high-dose ARB treatment.

Objective: To study the long-term safety of high-dose ARB treatment.

Methods: We observed 48 patients [44 men and 4 women; ages 64 +/- 15 years (mean +/- SD), weight 88 +/- 28 kg, estimated glomerular filtration rate 53 +/- 23 ml/min] receiving treatment with high doses (1.5-5 times greater than the maximum approved dose) of ARBs, for 40 +/- 24 months (range 6-98 months).

Results: The average ARB dose tended to increase over time and was 3.2 +/- 1.2 times greater at the end of the study than that at the start. Systolic blood pressure was similar at the beginning and end of the study period (132 +/- 20 and 125 +/- 20 mmHg, respectively), but diastolic blood pressure showed a decrease throughout the study and was significantly reduced (P < 0.05) in association with 1.5x and 2x the maximum ARB dose (73 +/- 11 and 72 +/- 10 mmHg, respectively) when compared with baseline (78 +/- 11 mm Hg). There was a trend (P > 0.05) for increases in concentrations of serum potassium (0.2 +/- 0.9 mmol/l) and creatinine (0.3 +/- 0.7 mg/dl) with increases in dose from baseline to the end of the study. Serum creatinine concentration was greater (P < 0.05) at the periods of 3x and 4x the maximum dose, but this represented increases of only 12 and 20% from baseline, respectively.

Conclusions: High-dose ARB treatment in patients with chronic renal disease is not associated with any clinically significant long-term negative effects on serum creatinine or potassium and is thus a important therapeutic modality with which to achieve further reductions in urinary protein excretion.

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