Gong Yan, Huang Zhibi, Christensen Erik, Gluud Christian
The Cochrane Hepato-Biliary Group, Copenhagen Trial Unit, Center for Clinical Intervention Research, Department 7102, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Am J Gastroenterol. 2007 Aug;102(8):1799-807. doi: 10.1111/j.1572-0241.2007.01235.x. Epub 2007 Apr 24.
Ursodeoxycholic acid (UDCA) is used for primary biliary cirrhosis (PBC), but the beneficial effects remain controversial.
We performed an updated systematic review to evaluate the benefits and harms of UDCA in patients with PBC. We included randomized clinical trials evaluating UDCA versus placebo or no intervention in patients with PBC. The primary outcomes, mortality and mortality or liver transplantation, were reported as relative risk (RR) with 95% confidence interval (CI). Meta-regression was used to investigate the associations between UDCA effects and the trial's risk of bias, UDCA dose, duration, and PBC severity at trial entry. We used Bayesian meta-analytic approaches as sensitivity analyses.
Sixteen randomized clinical trials (1,447 patients) evaluating UDCA versus placebo or no intervention were identified. Over half of the trials had high risk of bias. Comparing with placebo or no intervention, UDCA did not significantly affect mortality (RR 0.97, 95% CI 0.67-1.42) and mortality or liver transplantation (RR 0.92, 95% CI 0.71-1.21). The findings were supported by the Bayesian meta-analyses. Meta-regression analyses suggested that UDCA effects seem to be associated with patient's disease severity and trial duration. UDCA did not improve pruritus, fatigue, autoimmune conditions, liver histology, or portal pressure. UDCA seemed to improve biochemical variables, such as serum bilirubin, and ascites and jaundice, but the findings were based on few trials with sparse data. The use of UDCA was significantly associated with adverse events, mainly weight gain.
This updated systematic review did not demonstrate any benefit of UDCA on mortality and mortality or liver transplantation in patients with PBC.
熊去氧胆酸(UDCA)用于原发性胆汁性肝硬化(PBC),但其有益效果仍存在争议。
我们进行了一项更新的系统评价,以评估UDCA对PBC患者的利弊。我们纳入了评估UDCA与安慰剂或不干预相比在PBC患者中的随机临床试验。主要结局,即死亡率以及死亡率或肝移植,报告为相对风险(RR)及95%置信区间(CI)。采用Meta回归研究UDCA效果与试验偏倚风险、UDCA剂量、疗程以及试验入组时PBC严重程度之间的关联。我们采用贝叶斯Meta分析方法作为敏感性分析。
确定了16项评估UDCA与安慰剂或不干预相比的随机临床试验(1447例患者)。超过半数的试验存在高偏倚风险。与安慰剂或不干预相比,UDCA对死亡率(RR 0.97,95%CI 0.67 - 1.42)以及死亡率或肝移植(RR 0.92,95%CI 0.71 - 1.21)无显著影响。这些结果得到了贝叶斯Meta分析的支持。Meta回归分析表明,UDCA的效果似乎与患者疾病严重程度和试验疗程有关。UDCA并未改善瘙痒、疲劳、自身免疫状况、肝脏组织学或门静脉压力。UDCA似乎改善了生化指标,如血清胆红素,以及腹水和黄疸,但这些结果基于少数数据稀少的试验。使用UDCA与不良事件显著相关,主要是体重增加。
这项更新的系统评价未证明UDCA对PBC患者的死亡率以及死亡率或肝移植有任何益处。