Agrawal Rohit, Majeed Muhammad, Attar Bashar M, Omar Yazan Abu, Mbachi Chimezie, Wang Yanting, Flores Estefania, Shaqib Shami, Wang Yuchen, Udechukwu Victor, Demetria Melchor, Gandhi Seema
Department of Medicine (Rohit Agrawal, Muhammad Majeed, Yazan Abu Omar, Chimezie Mbachi, Yanting Wang, Estefania Flores, Shami Shaqib, Yuchen Wang, Melchor Demetria).
Department of Division of Gastroenterology and Hepatology, Department of Medicine (Bashar M. Attar, Melchor Demetria, Seema Gandhi), Cook County Health and Hospital System, County, Chicago, IL, USA.
Ann Gastroenterol. 2019 Sep-Oct;32(5):489-497. doi: 10.20524/aog.2019.0403. Epub 2019 Jul 22.
Ursodeoxycholic acid (UDCA) and obeticholic acid are currently approved treatments for primary biliary cholangitis (PBC). Since some patients do not respond adequately to UDCA, other therapies, such as bezafibrate, have been developed. In this meta-analysis we evaluated the efficacy and safety of using both UDCA and bezafibrate in patients with an inadequate response to UDCA.
We evaluated all randomized controlled trials comparing the combination of UDCA and bezafibrate with UDCA monotherapy. Standardized mean difference (SMD) was used to assess the treatment effect of combination therapy compared with UDCA alone.
Ten trials with a total of 369 patients were analyzed. UDCA and bezafibrate combination therapy was more effective than UDCA monotherapy in improving alanine aminotransferase (SMD -2.04, 95% confidence interval [CI] -3.30 to -0.79), alkaline phosphatase at both less than 12 months (SMD -3.63, 95%CI -6.43 to -0.84) and more than 12 months (SMD -2.33, 95%CI -4.03 to -0.63), gamma-glutamyltransferase (SMD -1.29, 95%CI -2.67 to 0.08), triglyceride (SMD -0.80, 95%CI -1.41 to -0.19), immunoglobulin M (SMD -1.48, 95%CI -2.39 to -0.56), and cholesterol (SMD -4.61, 95%CI -7.34 to -1.89). There was no difference between the 2 groups in bilirubin, aspartate aminotransferase or albumin. None of the adverse effects differed statistically between the 2 groups.
UDCA and bezafibrate combined treatment is superior to UDCA alone in UDCA non-responders with regard to decreasing liver biochemistry markers, without any significant increase in side effects in patients with PBC.
熊去氧胆酸(UDCA)和奥贝胆酸目前被批准用于治疗原发性胆汁性胆管炎(PBC)。由于一些患者对UDCA反应不佳,因此已开发出其他疗法,如苯扎贝特。在这项荟萃分析中,我们评估了在对UDCA反应不佳的患者中联合使用UDCA和苯扎贝特的疗效和安全性。
我们评估了所有比较UDCA与苯扎贝特联合治疗和UDCA单药治疗的随机对照试验。标准化均数差(SMD)用于评估联合治疗与单独使用UDCA相比的治疗效果。
分析了10项试验,共369例患者。在改善丙氨酸氨基转移酶方面,UDCA与苯扎贝特联合治疗比UDCA单药治疗更有效(SMD -2.04,95%置信区间[CI] -3.30至-0.79);在治疗不到12个月时碱性磷酸酶(SMD -3.63,95%CI -6.43至-0.84)和超过12个月时碱性磷酸酶(SMD -2.33,95%CI -4.03至-0.63)、γ-谷氨酰转移酶(SMD -1.29,95%CI -2.67至0.08)、甘油三酯(SMD -0.80,95%CI -1.41至-0.19)、免疫球蛋白M(SMD -1.48,95%CI -2.39至-0.56)和胆固醇(SMD -4.61,95%CI -7.34至-1.89)方面也是如此。两组在胆红素、天冬氨酸氨基转移酶或白蛋白方面无差异。两组之间的不良反应在统计学上均无差异。
对于PBC患者,在UDCA反应不佳者中,UDCA与苯扎贝特联合治疗在降低肝脏生化指标方面优于单独使用UDCA,且副作用无显著增加。