Xiao Huan-Ming, Shi Mei-Jie, Jiang Jun-Min, Cai Gao-Shu, Xie Yu-Bao, Tian Guang-Jun, Xue Jing-Dong, Mao De-Wen, Li Qin, Yang Hong-Zhi, Guo Hui, Lei Chun-Liang, Lu Wei, Chen Liang, Liu Hua-Bao, Wang Jing, Gao Yue-Qiu, Chen Jie-Zhen, Wu Shu-Duo, Chen Hui-Jun, Zhao Peng-Tao, Zhang Chao-Zhen, Ou-Yang Wen-Wei, Wen Ze-Huai, Chi Xiao-Ling
Hepatology Department, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.
Liver Diseases Branch, Shaanxi Provincial Hospital of Traditional Chinese Medicine, Xi'an, 710003, China.
J Ethnopharmacol. 2022 Jul 15;293:115210. doi: 10.1016/j.jep.2022.115210. Epub 2022 Apr 7.
The AnluoHuaxian pill (AHP) is a widely used patented medicine for chronic hepatitis B (CHB) patients with advanced fibrosis or cirrhosis that has been used in China for more than 15 years. However, data are lacking on whether monotherapy with AHP can be effective in CHB patients with alanine aminotransferase (ALT) levels less than 2 times the upper limit of normal (ALT<2ULN) and early liver fibrosis (F ≤ 2).
We aimed to investigate whether monotherapy with AHP improves liver histology in these patients.
In this double-blind, randomized, placebo-controlled trial, 270 CHB patients with ALT<2ULN and F ≤ 2 were treated in 12 hospitals in China. The patients were randomly assigned to an intervention (AHP) group and a placebo group at a ratio of 2:1. Of these 270 enrolled patients, 147 had paired liver biopsies. The primary end point was histological change after 48 weeks of treatment.
Per-protocol analysis revealed that the rate of histologic improvement in liver fibrosis patients in the AHP group was significantly higher than that in the placebo group (37.7% vs. 19.5%, P = 0.035) after 48 weeks of treatment, which was consistent with results from intention-to-treat and sensitivity analyses. Moreover, after adjusting for baseline characteristics, AHP was superior to placebo with respect to improving liver fibrosis (odds ratio [OR] = 2.58, 95% confidence interval [CI]: (1.01, 6.63),P = 0.049) and liver histology (OR = 3.62, 95% CI: (1.42, 9.20),P = 0.007). In noninvasive measurement of liver fibrosis (FibroScan®), the level of liver stiffness measurement (LSM) had decreased significantly at 48 weeks (5.1 kPa) compared with that at baseline (5.7 kPa) (P = 0.008) in the AHP group, whereas it did not decrease significantly in the placebo group. Cirrhosis developed in one patient in the placebo group but in no patients in the AHP group. No serious side effects occurred in the AHP-treated patients.
Treatment of CHB patients who had ALT<2ULN and F ≤ 2 with the traditional Chinese medicine AHP for 48 weeks improves liver fibrosis. However, due to the short duration of treatment and the limited sample size of liver pathology, the long-term benefits of AHP in reducing fibrosis and the risk of cirrhosis and hepatocellular carcinoma in these patients need to be further studied in the future.
安络化纤丸(AHP)是一种在中国已应用超过15年的、广泛用于治疗晚期纤维化或肝硬化慢性乙型肝炎(CHB)患者的专利药物。然而,关于AHP单药治疗对丙氨酸氨基转移酶(ALT)水平低于正常上限2倍(ALT<2ULN)且有早期肝纤维化(F≤2)的CHB患者是否有效,目前尚缺乏相关数据。
我们旨在研究AHP单药治疗能否改善这些患者的肝脏组织学。
在这项双盲、随机、安慰剂对照试验中,中国12家医院的270例ALT<2ULN且F≤2的CHB患者参与研究。患者按2:1的比例随机分为干预(AHP)组和安慰剂组。在这270例入组患者中,147例进行了配对肝脏活检。主要终点是治疗48周后的组织学变化。
符合方案分析显示,治疗48周后,AHP组肝纤维化患者的组织学改善率显著高于安慰剂组(37.7%对19.5%,P = 0.035),这与意向性分析和敏感性分析结果一致。此外,在调整基线特征后,AHP在改善肝纤维化(优势比[OR]=2.58,95%置信区间[CI]:(1.01, 6.63),P = 0.049)和肝脏组织学(OR = 3.62,95%CI:(1.42, 9.20),P = 0.007)方面优于安慰剂。在肝纤维化的非侵入性测量(FibroScan®)中,AHP组在48周时肝脏硬度测量(LSM)水平较基线时(5.7 kPa)显著降低(5.1 kPa)(P = 0.008),而安慰剂组未显著降低。安慰剂组有1例患者发生肝硬化,而AHP组无患者发生。接受AHP治疗的患者未出现严重副作用。
用中药AHP治疗ALT<2ULN且F≤2的CHB患者48周可改善肝纤维化。然而,由于治疗时间短且肝脏病理学样本量有限,AHP在降低这些患者纤维化、肝硬化和肝细胞癌风险方面的长期益处未来还需进一步研究。