| Literature DB >> 28565796 |
Jianrong Wang1, Wenxia Lu2, Jingjing Li3, Rong Zhang2, Yuqing Zhou4, Qin Yin4, Yuanyuan Zheng3, Fan Wang3, Yujing Xia3, Kan Chen3, Sainan Li3, Tong Liu3, Jie Lu3, Yingqun Zhou3, Chuan-Yong Guo3.
Abstract
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.Entities:
Keywords: aldosterone antagonist; angiotensin I-converting enzyme inhibitor; angiotensin receptor blocker; hepatic venous pressure gradient; portal hypertension; β-blockers
Year: 2017 PMID: 28565796 PMCID: PMC5443179 DOI: 10.3892/etm.2017.4210
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447