中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

熊去氧胆酸联合甘草酸二铵治疗原发性胆汁性胆管炎的效果观察

张玉果 赵素贤 李文聪 任伟光 南月敏

引用本文:
Citation:

熊去氧胆酸联合甘草酸二铵治疗原发性胆汁性胆管炎的效果观察

DOI: 10.3969/j.issn.1001-5256.2019.06.028
基金项目: 

中国肝炎防治基金会-天晴肝病研究基金(TQGB20140203); 河北省中医药管理局课题(2014143); 

详细信息
  • 中图分类号: R575.7

Clinical effect of ursodeoxycholic acid combined with diammonium glycyrrhizinate in treatment of primary biliary cholangitis

Research funding: 

 

  • 摘要:

    目的对比熊去氧胆酸(UDCA)联合甘草酸二铵与单用UDCA治疗原发性胆汁性胆管炎(PBC)的生化学应答和肝脏硬度变化情况。方法选取2014年1月-2016年3月就诊于河北医科大学第三医院中西医结合肝病科的PBC患者66例,均行FibroTouch检测,以肝脏硬度值表示肝纤维化程度,对比分析UDCA联合甘草酸二铵与单用UDCA治疗PBC患者4、12、24和48周的肝生化学应答和治疗24、48周后肝脏硬度值变化情况。两组间计量资料比较采用两独立样本t检验,治疗前后生化学指标及肝脏硬度值比较采用配对t检验。结果 UDCA联合甘草酸二铵治疗组与单用UDCA对照组比较,联合治疗组AST水平在治疗后4周[(38. 4±15. 4) U/L vs (61. 6±28. 8) U/L,t=2. 684,P=0. 012]、12周[(36. 4±12. 6) U/L vs (58. 1±24. 8) U/L,t=2. 953,P=0. 006)]、24周[(37. 0±8. 5) U/L vs (52. 9±17. 2) U/L,t=3. 134,P=0. 004]、48周[(34. 9±7. 9) U...

     

  • [1]LINDOR KD, BOWLUS CL, BOYER J, et al.Primary biliary cholangitis:2018 practice guidance from the American Association for the Study of Liver Diseases[J].Hepatology, 2019, 69 (1) :394-419.
    [2]European Association for the Study of the Liver.EASL Clinical Practice Guidelines:The diagnosis and management of patients with primary biliary cholangitis[J].J Hepatol, 2017, 67 (1) :145-172.
    [3]Chinese Society of Hepatology, Chinese Medical Association;Chinese Society of Gastroenterology, Chinese Medical Association;Chinese Society of Infectious Diseases, Chinese Medical Association.Consensus on the diagnosis and management of primary biliary cirrhosis (cholangitis) (2015) [J].J Clin Hepatol, 2015, 31 (12) :1980-1988. (in Chinese) 中华医学会肝病学分会, 中华医学会消化病学分会, 中华医学会感染病学分会.原发性胆汁性肝硬化 (又名原发性胆汁性胆管炎) 诊断和治疗共识 (2015) [J].临床肝胆病杂志, 2015, 31 (12) :1980-1988.
    [4] Chinese Expert Committee for the diagnosis and treatment of cholestasis liver disease.Chinese expert consensus guidelines for the diagnosis and treatment of cholestasis liver disease reached in 2013[J/CD].Chin J Exp Clin Infect Dis:Electronic Edition, 2013, 7 (1) :134-144. (in Chinese) 胆汁淤积性肝病诊断治疗专家委员会.胆汁淤积性肝病诊断治疗专家共识2013[J/CD].中华实验和临床感染病杂志:电子版, 2013, 7 (1) :134-144.
    [5]ZHANG LN, SHI TY, SHI XH, et al.Early biochemical response to ursodeoxycholic acid and long-term prognosis of primary biliary cirrhosis:Results of a 14-year cohort study[J].Hepatology, 2013, 58 (1) :264-272.
    [6]CZUL F, LEVY C.Novel therapies on primary biliary cirrhosis[J].Clin Liver Dis, 2016, 20 (1) :113-130.
    [7]CORPECHOT C, ABENAVOLI L, RABAHI N, et al.Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis[J].Hepatology, 2008, 48 (3) :871-877.
    [8]NEVENS F, ANDREONE P, MAZZELLA G, et al.A placebocontrolled trial of obeticholic acid in primary biliary cholangitis[J].N Engl J Med, 2016, 375 (7) :631-643.
    [9]KOWDLEY KV, LUKETIC V, CHAPMAN R.A randomized trial of obeticholic acid monotherapy in patients with primary biliary cholangitis[J].Hepatology, 2018, 67 (5) :1890-1902.
    [10]DUAN WJ, OU XJ, WANG XM, et al.Efficacy and safety of fenofibrate add-on therapy for patients with primary biliary cholangitis and a suboptimal response to UDCA[J].Rev Esp Enferm Dig, 2018, 110 (9) :557-563.
    [11]ZHANG L, FAN YJ, TAN B, et al.Recognition of the clinical application and biological mechanism of ursodeoxycholic acid in liver diseases[J].Chin J Clin Pharmacol Ther, 2017, 22 (2) :233-240. (in Chinese) 张林, 樊玉娟, 谭波, 等.熊脱氧胆酸在慢性肝病中应用及机制的再认识[J].中国临床药理学与治疗学, 2017, 22 (2) :233-240.
    [12] CHEN JL, YANG X, ZHANG Q, et al.Effect of ursodeoxycholic acid with traditional Chinese medicine on biochemical response in patients with primary biliary cholangitis:A realworld cohort study[J].Chin J Hepatol, 2018, 26 (12) :909-915. (in Chinese) 陈佳良, 杨雪, 张群, 等.熊去氧胆酸联合中药治疗对原发性胆汁性胆管炎患者生物化学应答的影响:一项基于真实世界的队列研究[J].中华肝脏病杂志, 2018, 26 (12) :909-915.
    [13]ZHAO ZB, LIAN ZX.Immunological pathogenesis of primary biliary cholangitis[J].J Clin Hepatol, 2017, 33 (11) :2112-2116. (in Chinese) 赵志斌, 廉哲雄.原发性胆汁性胆管炎的免疫学发病机制[J].临床肝胆病杂志, 2017, 33 (11) :2112-2116.
    [14]CORPECHOT C, CARRAT F, POUJOL-ROBERT A, et al.Noninvasive elastography-based assessment of liver fibrosis progression and prognosis in primary biliary cirrhosis[J].Hepatology, 2012, 56 (1) :198-208.
    [15]CARBONE M, SHARP SJ, FLACK S, et al.The UK-PBC risk scores:Derivation and validation of a scoring system for long-term prediction of end-stage liver disease in primary biliary cholangitis[J].Hepatology, 2016, 63 (3) :930-950.
    [16]LAMMERS WJ, HIRSCHFIELD GM, CORPECHOT C, et al.Development and validation of a scoring system to predict outcomes of patients with primary biliary cirrhosis receiving ursodeoxycholic acid therapy[J].Gastroenterology, 2015, 149 (7) :1804-1812.
  • 加载中
计量
  • 文章访问数:  1793
  • HTML全文浏览量:  52
  • PDF下载量:  304
  • 被引次数: 0
出版历程
  • 收稿日期:  2019-02-14
  • 出版日期:  2019-06-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回