Inaguma Daijo, Ito Eri, Koide Shigehisa, Takahashi Kazuo, Hayashi Hiroki, Hasegawa Midori, Yuzawa Yukio
Fujita Health University School of Medicine, Toyoake, Japan.
Cardiorenal Med. 2017 Dec;8(1):71-81. doi: 10.1159/000479894. Epub 2017 Nov 3.
Several human studies reported that the combined use of renin-angiotensin system blockers (RASBs) and vitamin D receptor activators (VDRAs) resulted in decreased urinary protein excretion. However, it is unknown whether this combination therapy influences the incidence of cardiovascular (CV) events in dialysis patients.
The study was a multicenter nonrandomized prospective cohort analysis including 1,518 patients. Patients were classified into 4 groups based on medications prescribed before dialysis initiation: those who did not receive RASBs or oral VDRAs (N group), those receiving only RASBs, those receiving only VDRAs, and those receiving a combination of RASBs and VDRAs (RD group). CV events after dialysis initiation were compared using the log-rank test. Factors contributing to the incidence of CV events were examined using multivariate Cox proportional hazard regression analysis.
Significant differences were observed in the incidence of CV events and all-cause mortality between the 4 groups ( = 0.021 and = 0.001, respectively). Cox proportional hazard analysis revealed that the incidence of CV events was significantly lower in the RD group than in the N group (hazard ratio [HR] = 0.65, 95% confidence interval [CI]: 0.50-0.86, = 0.002). Multivariate analysis revealed that the incidence of CV events was significantly lower in the RD group than in the N group (HR = 0.66, 95% CI: 0.47-0.93, = 0.016).
Combination therapy with RASBs and VDRAs in patients before dialysis initiation was associated with a reduction in CV events during maintenance dialysis.
多项人体研究报告称,联合使用肾素 - 血管紧张素系统阻滞剂(RASBs)和维生素D受体激活剂(VDRAs)可降低尿蛋白排泄。然而,这种联合治疗是否会影响透析患者心血管(CV)事件的发生率尚不清楚。
该研究是一项多中心非随机前瞻性队列分析,包括1518例患者。根据透析开始前开具的药物将患者分为4组:未接受RASBs或口服VDRAs的患者(N组)、仅接受RASBs的患者、仅接受VDRAs的患者以及接受RASBs和VDRAs联合治疗的患者(RD组)。使用对数秩检验比较透析开始后的CV事件。使用多变量Cox比例风险回归分析检查导致CV事件发生率的因素。
4组之间在CV事件发生率和全因死亡率方面观察到显著差异(分别为 = 0.021和 = 0.001)。Cox比例风险分析显示,RD组的CV事件发生率显著低于N组(风险比[HR] = 0.65,95%置信区间[CI]:0.50 - 0.86, = 0.002)。多变量分析显示,RD组的CV事件发生率显著低于N组(HR = 0.66,95% CI:0.47 - 0.93, = 0.016)。
透析开始前患者使用RASBs和VDRAs联合治疗与维持性透析期间CV事件的减少有关。