Xia Yun, Luo Hui, Liu Jian Ping, Gluud Christian
Centre for Evidence-Based Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Cochrane Database Syst Rev. 2011 Apr 13(4):CD008960. doi: 10.1002/14651858.CD008960.pub2.
Phyllanthus species for patients with chronic hepatitis B virus (HBV) infection have been assessed in clinical trials, but no consensus regarding their usefulness exists.
To evaluate the benefits and harms of phyllanthus species for patients with chronic HBV infection.
Searches were performed in The Cochrane Hepato-Biliary Gorup Controlled Trials Register, The Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library, MEDLINE, EMBASE, Science Citation Index Expanded, and the Chinese Biomedical CD Database, China Network Knowledge Information, Chinese Science Journal Database, TCM Online, and Wanfang Database. Conference proceedings in Chinese were handsearched. All searches were conducted until October 2010.
Randomised clinical trials comparing phyllanthus species with placebo or no intervention for patients with chronic HBV infection. Co-interventions were allowed if all comparison groups had received the same co-interventions. We included trials irrespective of blinding, publication status, or language.
Two authors selected the trials and extracted the data independently. The RevMan software was used for statistical analysis of dichotomous data with risk ratio (RR) with 95% confidence intervals (CI). Risk of bias was assessed to control for systematic errors. Trial sequential analysis was used in order to control for random errors.
A total of 16 randomised trials with 1326 patients were included. One trial with 42 participants compared phyllanthus with placebo. The trial found no significant difference in HBeAg seroconversion after the end of treatment (RR 0.9; 95% CI 0.73 to 1.25) or follow-up (RR 1.00; 95% CI 0.63 to 1.60). No other outcomes could be assessed. Fifteen trials compared phyllanthus plus an antiviral drug like interferon alpha, lamivudine, adefovir dipivoxil, thymosin, vidarabine, or conventional treatment with the same antiviral drug alone. Phyllanthus did significantly affect serum HBV DNA (RR 0.69; 95% CI 0.52 to 0.91, P = 0.008; I(2) = 71%), serum HBeAg (RR 0.70; 95% CI 0.60 to 0.81, P < 0.00001; I(2) = 68%), and HBeAg seroconversion (RR 0.77; 95% CI 0.63 to 0.92, P = 0.005; I(2) = 78%), but the heterogeneity was substantial. The result obtained regarding serum HBV DNA was not supported by trial sequential analysis. None of the trials reported mortality and hepatitis B-related morbidity, quality of life, or liver histology. Only two trials reported adverse events with numbers without significant differences. No serious adverse events were reported.
AUTHORS' CONCLUSIONS: There is no convincing evidence that phyllanthus compared with placebo benefits patients with chronic HBV infection. Phyllanthus plus an antiviral drug may be better than the same antiviral drug alone. However, heterogeneity, systematic errors, and random errors question the validity of the results. Clinical trials with large sample size and low risk of bias are needed to confirm our findings. Species of phyllanthus should be reported in future trials, and a dose-finding design is warranted.
在临床试验中已对叶下珠属植物用于慢性乙型肝炎病毒(HBV)感染患者的情况进行了评估,但对于其有效性尚未达成共识。
评估叶下珠属植物对慢性HBV感染患者的益处和危害。
检索了Cochrane肝胆组对照试验注册库、Cochrane图书馆中的Cochrane对照试验中央注册库(CENTRAL)、MEDLINE、EMBASE、科学引文索引扩展版,以及中国生物医学光盘数据库、中国知网、中国科学期刊数据库、中医在线和万方数据库。手工检索了中文会议论文集。所有检索截至2010年10月。
比较叶下珠属植物与安慰剂或对慢性HBV感染患者不进行干预的随机临床试验。如果所有比较组接受相同的联合干预措施,则允许采用联合干预。我们纳入的试验不考虑是否采用盲法、发表状态或语言。
两位作者独立选择试验并提取数据。使用RevMan软件对二分类数据进行统计分析,计算风险比(RR)及95%置信区间(CI)。评估偏倚风险以控制系统误差。采用试验序贯分析以控制随机误差。
共纳入16项随机试验,涉及1326例患者。一项纳入42例参与者的试验比较了叶下珠与安慰剂。该试验发现在治疗结束后HBeAg血清学转换(RR 0.9;95%CI 0.73至1.25)或随访时(RR 1.00;95%CI 0.63至1.60)无显著差异。无法评估其他结局。15项试验比较了叶下珠联合干扰素α、拉米夫定、阿德福韦酯、胸腺素、阿糖腺苷等抗病毒药物或传统治疗与单纯使用相同抗病毒药物的效果。叶下珠确实对血清HBV DNA(RR 0.69;95%CI 0.52至0.91,P = 0.008;I² = 71%)、血清HBeAg(RR 0.70;95%CI 0.60至0.81,P < 0.00001;I² = 68%)和HBeAg血清学转换(RR 0.77;95%CI 0.63至0.92,P = 0.005;I² = 78%)有显著影响,但异质性较大。试验序贯分析不支持关于血清HBV DNA的结果。没有试验报告死亡率、乙型肝炎相关发病率、生活质量或肝脏组织学情况。只有两项试验报告了不良事件的数量,无显著差异。未报告严重不良事件。
没有令人信服的证据表明与安慰剂相比,叶下珠对慢性HBV感染患者有益。叶下珠联合抗病毒药物可能比单纯使用相同抗病毒药物效果更好。然而,异质性、系统误差和随机误差对结果的有效性提出了质疑。需要开展大样本量且偏倚风险低的临床试验来证实我们的发现。未来试验应报告叶下珠的种类,且有必要采用剂量探索设计。