Wang Jianrong, Lu Wenxia, Li Jingjing, Zhang Rong, Zhou Yuqing, Yin Qin, Zheng Yuanyuan, Wang Fan, Xia Yujing, Chen Kan, Li Sainan, Liu Tong, Lu Jie, Zhou Yingqun, Guo Chuan-Yong
Department of Gastroenterology, Nanjing Jiangbei People's Hospital Affiliated to Nantong University, Nanjing, Jiangsu 210048, P.R. China.
The First Clinical Medical College of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Exp Ther Med. 2017 May;13(5):1977-1985. doi: 10.3892/etm.2017.4210. Epub 2017 Mar 9.
β-blockers are commonly used for the treatment of acute variceal bleeding in cirrhosis. Renin-angiotensin-aldosterone antagonists (angiotensin I-converting enzyme inhibitors, angiotensin receptor blockers and aldosterone antagonists) are potential therapies for portal hypertension. Several studies have compared the renin-angiotensin-aldosterone system (RAAS) inhibitor and β-blocker combination therapy vs. β-blocker monotherapy, with inconsistent results. The aim of the present study was to assess the efficacy of the RAAS inhibitor and β-blocker combination therapy vs. β-blocker monotherapy for hepatic vein pressure gradient (HVPG) reduction in cirrhosis. Studies were obtained using PubMed, Embase, Medline and Cochrane library databases up to July 2015, and the weighted mean difference (WMD) in HVPG reduction was used as a measure of treatment efficacy. In total, three studies (91 patients) were included. When compared to the β-blocker monotherapy, the RAAS inhibitor and β-blocker combination therapy resulted in a significant HVPG reduction [WMD 1.70; 95% confidence interval (CI): 0.52-2.88]. However, there was no significant difference in the heart rate reduction between the monotherapy and combination therapy groups (WMD -0.11; 95% CI: -3.51-3.29). In addition, no significant difference in the hemodynamic response was observed between the two groups (WMD 1.46; 95% CI: 0.93-2.30). In conclusion, the RAAS inhibitor and β-blocker combination therapy reduces portal hypertension significantly and to a greater extent than β-blocker monotherapy. Both therapies reduced the heart rate to similar levels; however, the RAAS inhibitor and β-blocker combination therapy reduced the mean arterial pressure to a greater extent. Due to the limited number of studies included, the data available do not allow a satisfactory comparison of adverse events. Moreover, further larger-scale trials are required in order to strengthen the results of the present study.
β受体阻滞剂常用于治疗肝硬化急性静脉曲张出血。肾素 - 血管紧张素 - 醛固酮拮抗剂(血管紧张素I转换酶抑制剂、血管紧张素受体阻滞剂和醛固酮拮抗剂)是门静脉高压的潜在治疗方法。多项研究比较了肾素 - 血管紧张素 - 醛固酮系统(RAAS)抑制剂与β受体阻滞剂联合治疗与β受体阻滞剂单药治疗的效果,结果不一致。本研究的目的是评估RAAS抑制剂与β受体阻滞剂联合治疗与β受体阻滞剂单药治疗在降低肝硬化患者肝静脉压力梯度(HVPG)方面的疗效。检索了截至2015年7月的PubMed、Embase、Medline和Cochrane图书馆数据库中的研究,并将HVPG降低的加权平均差(WMD)用作治疗效果的衡量指标。总共纳入了三项研究(91例患者)。与β受体阻滞剂单药治疗相比,RAAS抑制剂与β受体阻滞剂联合治疗导致HVPG显著降低[WMD 1.70;95%置信区间(CI):0.52 - 2.88]。然而,单药治疗组与联合治疗组在心率降低方面无显著差异(WMD -0.11;95% CI:-3.51 - 3.29)。此外,两组在血流动力学反应方面未观察到显著差异(WMD 1.46;95% CI:0.93 - 2.30)。总之,RAAS抑制剂与β受体阻滞剂联合治疗比β受体阻滞剂单药治疗能更显著地降低门静脉高压。两种治疗方法都将心率降低到相似水平;然而,RAAS抑制剂与β受体阻滞剂联合治疗在更大程度上降低了平均动脉压。由于纳入的研究数量有限,现有数据无法对不良事件进行令人满意的比较。此外,需要进一步开展更大规模的试验以强化本研究结果。