Titan S M, M Vieira J, Dominguez W V, Barros R T, Zatz R
Renal Division, Department of Clinical Medicine, University of São Paulo, Brazil.
Clin Nephrol. 2011 Oct;76(4):273-83. doi: 10.5414/cn107013.
The combination of an ACE inhibitor (ACEI) and an angiotensin II receptor blocker (ARB) has been proposed for the treatment of diabetic nephropathy (DN), but doubts remain about its efficacy and safety. We compared the effects of combination therapy and ACEI monotherapy on proteinuria and on three urinary inflammatory cytokines (MCP-1, TGF-beta and VEGF).
56 patients with macroalbuminuric DN received 40 mg/d enalapril for 4 months, followed by add-on 100 mg/day losartan or placebo for another 4 months. The primary and secondary endpoints were reduction of proteinuria and cytokine levels, respectively.
Proteinuria did not fall in either group. Repeated measures ANOVA revealed no difference between groups. A high side effect rate was observed (28.5%). Finally, unadjusted logistic regression showed no difference between groups, but after adjustments the risk of worsening proteinuria was higher in the combination therapy group (p = 0.04). The same pattern was observed for urinary MCP- 1.
These results suggest that 1) in advanced DN with severe proteinuria and poor metabolic control, angiotensin II blockade may be less effective than in other groups of CKD patients. 2) In such patients, combination therapy may not afford superior renoprotection compared to enalapril. 3) Urinary MCP-1 is a promising biomarker for the response to ACEI and/or ARB treatment and for the risk of associated unwanted effects.
已有人提出将血管紧张素转换酶抑制剂(ACEI)与血管紧张素II受体阻滞剂(ARB)联合用于治疗糖尿病肾病(DN),但其疗效和安全性仍存疑问。我们比较了联合治疗与ACEI单药治疗对蛋白尿及三种尿炎性细胞因子(MCP-1、转化生长因子-β和血管内皮生长因子)的影响。
56例大量白蛋白尿型DN患者接受40mg/d依那普利治疗4个月,随后加用100mg/d氯沙坦或安慰剂再治疗4个月。主要终点和次要终点分别为蛋白尿减少和细胞因子水平降低。
两组蛋白尿均未下降。重复测量方差分析显示两组间无差异。观察到较高的副作用发生率(28.5%)。最后,未经调整的逻辑回归显示两组间无差异,但调整后联合治疗组蛋白尿恶化风险更高(p = 0.04)。尿MCP-1也观察到相同模式。
这些结果表明:1)在晚期DN伴严重蛋白尿和代谢控制不佳的患者中,血管紧张素II阻断可能不如其他慢性肾脏病患者有效。2)在此类患者中,联合治疗相比于依那普利可能无法提供更好的肾脏保护作用。3)尿MCP-1是一种有前景的生物标志物,可用于评估对ACEI和/或ARB治疗的反应以及相关不良反应的风险。