Nakayama Y, Inoue T, Kohda Y, Inoue H, Izumi Y, Tomita K, Nonoguchi H
Department of Nephrology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Clin Nephrol. 2008 Jun;69(6):402-7. doi: 10.5414/cnp69402.
Recently, we reported the effectiveness of PAC therapy, a combination therapy with prostaglandin (PG) and angiotensin-converting enzyme inhibitor (ACE-I), as a new tool for the prevention of chronic kidney disease. In the current study, we continually treated these patients with or without PG and analyzed the survival rate of renal function by Kaplan-Meier method and Cox regression analysis.
52 patients (serum creatinine 2.9 A+/- 1.9 mg/dl) were followed-up for 48 months. 26 patients continued to receive ACE-I monotherapy and the remaining 26 patients were treated by PAC therapy. Primary end-point was defined as a decrease in 1/Cr by 0.2 (dl/mg), initiation of renal replacement therapy or death.
At the end of the study, PAC therapy significantly reduced the risk for the decline in renal function compared to ACE-I monotherapy by 54%. Survival time was longer in PAC group (21.7 A+/- 2.2 and 35.1 A+/- 3.9 months, in ACE-I monotherapy and PAC therapy, p < 0.05). Cox regression analysis indicated that age, sex and blood pressure except urinary protein excretion did not relate to the risk reduction by PAC therapy.
PAC therapy was proved to reduce the progression of end-stage renal failure.
最近,我们报道了前列腺素(PG)与血管紧张素转换酶抑制剂(ACE-I)联合治疗(PAC疗法)作为预防慢性肾脏病新方法的有效性。在本研究中,我们继续对这些患者进行有无PG治疗,并通过Kaplan-Meier法和Cox回归分析来分析肾功能的生存率。
52例患者(血清肌酐2.9±1.9mg/dl)接受了48个月的随访。26例患者继续接受ACE-I单药治疗,其余26例患者接受PAC疗法。主要终点定义为肌酐清除率倒数下降0.2(dl/mg)、开始肾脏替代治疗或死亡。
在研究结束时,与ACE-I单药治疗相比,PAC疗法使肾功能下降风险显著降低了54%。PAC组的生存时间更长(ACE-I单药治疗组为21.7±2.2个月,PAC疗法组为35.1±3.9个月,p<0.05)。Cox回归分析表明,除尿蛋白排泄外,年龄、性别和血压与PAC疗法降低风险无关。
PAC疗法被证明可降低终末期肾衰竭的进展。