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

非诺贝特联合熊去氧胆酸治疗单用熊去氧胆酸应答不佳的原发性胆汁性胆管炎患者的效果评价

王璐 孙可帅 韩者艺 郭长存 贾桂 高可娜 张亚维 韩英

王璐, 孙可帅, 韩者艺, 郭长存, 贾桂, 高可娜, 张亚维, 韩英. 非诺贝特联合熊去氧胆酸治疗单用熊去氧胆酸应答不佳的原发性胆汁性胆管炎患者的效果评价[J]. 临床肝胆病杂志, 2018, 34(11): 2368-2372. DOI: 10.3969/j.issn.1001-5256.2018.11.020.
引用本文: 王璐, 孙可帅, 韩者艺, 郭长存, 贾桂, 高可娜, 张亚维, 韩英. 非诺贝特联合熊去氧胆酸治疗单用熊去氧胆酸应答不佳的原发性胆汁性胆管炎患者的效果评价[J]. 临床肝胆病杂志, 2018, 34(11): 2368-2372. DOI: 10.3969/j.issn.1001-5256.2018.11.020.
Wang Lu, Sun KeShuai, Han ZheYi, Guo ZhangCun, Jia Gui, Gao KeNa, Zhang YaWei, Han Ying. Clinical effect of fenofibrate combined with ursodeoxycholic acid in treatment of primary biliary cholangitis patients with poor response to ursodeoxycholic acid alone[J]. J Clin Hepatol, 2018, 34(11): 2368-2372. DOI: 10.3969/j.issn.1001-5256.2018.11.020.
Citation: Wang Lu, Sun KeShuai, Han ZheYi, Guo ZhangCun, Jia Gui, Gao KeNa, Zhang YaWei, Han Ying. Clinical effect of fenofibrate combined with ursodeoxycholic acid in treatment of primary biliary cholangitis patients with poor response to ursodeoxycholic acid alone[J]. J Clin Hepatol, 2018, 34(11): 2368-2372. DOI: 10.3969/j.issn.1001-5256.2018.11.020.

非诺贝特联合熊去氧胆酸治疗单用熊去氧胆酸应答不佳的原发性胆汁性胆管炎患者的效果评价

DOI: 10.3969/j.issn.1001-5256.2018.11.020
基金项目: 

国家自然科学基金(81600451,81770569); 陕西省自然科学基础研究计划(2017JQ8009); 

详细信息
  • 中图分类号: R575.7

Clinical effect of fenofibrate combined with ursodeoxycholic acid in treatment of primary biliary cholangitis patients with poor response to ursodeoxycholic acid alone

Research funding: 

 

  • 摘要:

    目的探讨非诺贝特联合熊去氧胆酸(UDCA)治疗单用熊去氧胆酸应答不佳的原发性胆汁性胆管炎(PBC)患者的效果。方法选取2009年5月-2017年12月于空军军医大学西京消化病医院就诊的UDCA应答不佳PBC患者67例,根据是否加用非诺贝特分为联合治疗组33例、UDCA单药治疗组34例。收集2组患者基线(UDCA治疗1年时)和治疗后第6、12个月的临床资料,对比2组患者治疗后血清生化指标、生化应答反应、GLOBE评分。正态分布的计量资料2组间比较采用t检验;非正态分布的计量资料2组间比较采用Mann-Whitney U检验。计数资料2组间比较采用χ2检验或Fisher精确检验分析。结果治疗后第12个月,联合治疗组血清ALP、AST、ALT和GGT水平较单药UDCA组明显降低,差异均有统计学意义(t值分别为3. 465、2. 406、2. 057、3. 208,P值分别为<0. 001、0. 019、0. 002、0. 044)。根据巴塞罗那标准、ParisⅠ、Ⅱ标准,联合治疗组治疗12个月后的生化应答率分别为54. 5%(18/15)、36. 4%(12/21...

     

  • [1] HIRSCHFIELD GM, BEUERS U, CORPECHOT C, et al. EASL clinical practice guidelines:The diagnosis and management of patients with primary biliary cholangitis[J]. J Hepatol, 2017, 67 (1) :145-172.
    [2] TRIVEDI PJ, LAMMERS WJ, van BUUREN HR, et al. Stratification of hepatocellular carcinoma risk in primary biliary cirrhosis:A multicentre international study[J]. Gut, 2016, 65 (2) :321-329.
    [3] SHI YW, YOU H. Therapeutic strategies for patients with primary biliary cholangitis and suboptimal response to ursodeoxycholic acid[J]. J Clin Hepatol, 2017, 33 (11) :2101-2104. (in Chinese) 施漪雯, 尤红.对熊去氧胆酸应答不佳的原发性胆汁性胆管炎治疗策略[J].临床肝胆病杂志, 2017, 33 (11) :2101-2104.
    [4] ANGULO P, JORGENSEN RA, KEACH JC, et al. Oral budesonide in the treatment of patients with primary biliary cirrhosis with a suboptimal response to ursodeoxycholic acid[J]. Hepatology, 2000, 31 (2) :318-323.
    [5] NISANNE SG, MEENAKSHISUNDARAM A, CAROL JS, et al.Peroxisome proliferator-activated receptorαactivates human multidrug resistance transporter 3/ATP-binding cassette protein subfamily B4 transcription and increases rat biliary phosphatidylcholine secretion[J]. Hepatology, 2014, 59 (3) :1030-1042.
    [6] AKIRA H, TADASHI I, MAKOTO N, et al. Anticholestatic effects of bezafibrate in patients with primary biliary cirrhosis treated with ursodeoxycholic acid[J]. Hepatology, 2013, 57 (5) :1931-1941.
    [7] GHONEM NS, ASSIS DN, BOYER JL. Fibrates and cholestasis[J]. Hepatology, 2015, 62 (2) :635-643.
    [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] CUPERUS FJ, HALILBASIC E, TRAUNER M. Fibrate treatment for primary biliary cirrhosis[J]. Curr Opin Gastroenterol, 2014, 30 (3) :279-286.
    [10] GHONEM NS, BOYER JL. Fibrates as adjuvant therapy for chronic cholestatic liver disease:Its time has come[J]. Hepatology, 2013, 57 (5) :1691-1693.
    [11] CHEUNG AC, LAPOINTE-SHAW L, KOWGIER M, et al. Combined ursodeoxycholic acid (UDCA) and fenofibrate in primary biliary cholangitis patients with incomplete UDCA response may improve outcomes[J]. Aliment Pharmacol Ther, 2016, 43 (2) :283-293.
    [12] CORPECHOT C, CHAZOUILLèRES O, ROUSSEAU A, et al. A Placebo-Controlled Trial of Bezafibrate in Primary Biliary Cholangitis[J]. N Engl J Med, 2018, 378 (23) :2171-2181.
    [13] DUAN W, OU X, WANG X, 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.
    [14] HAN XF, WANG QX, LIU Y, et al. Efficacy of fenofibrate in Chinese patients with primary biliary cirrhosis partially responding to ursodeoxycholic acid therapy[J]. J Digest Dis, 2012, 13 (4) :219-224.
    [15] LINDOR KD, GERSHWIN ME, POUPON R, et al. AASLD practice guidelines:Primary biliary cirrhosis[J]. Hepatology, 2009, 50 (1) :291-308.
    [16] 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.
    [17] CORPECHOT C, CHAZOUILLERES O, POUPON R. Early primary biliary cirrhosis:Biochemical response to treatment and prediction of long-term outcome[J]. J Hepatol, 2011, 55 (6) :1361-1367.
    [18] PARES A, CABALLERIA L, RODES J. Excellent long-term survival in patients with primary biliary cirrhosis and biochemical response to ursodeoxycholic acid[J]. Gastroenterology, 2006, 130 (3) :715-720.
    [19] 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.e1804.
    [20] SPRINGER J, CAUCH-DUDEK K, O'ROURKE K, et al. Asymptomatic primary biliary cirrhosis:A study of its natural history and prognosis[J]. Am J Gastroenterol, 1999, 94 (1) :47.
    [21] MAHL TC, SHOCKCOR W, BOYER JL. Primary biliary cirrhosis:Survival of a large cohort of symptomatic and asymptomatic patients followed for 24 years[J]. J Hepatol, 1994, 20 (6) :707-713.
    [22] CHRISTENSEN E, CROWE J, DONIACH D, et al. Clinical pattern and course of disease in primary biliary cirrhosis based on an analysis of 236 patients[J]. Gastroenterology, 1980, 78 (2) :236-246.
    [23] de VRIES E, BEUERS U. Management of cholestatic disease in2017[J]. Liver Int, 2017, 37 (Suppl 1) :123-129.
    [24] KUMAGI T, GUINDI M, FISCHER SE, et al. Baseline Ductopenia and treatment response predict long-term histological progression in primary biliary cirrhosis[J]. Am J Gastroenterol, 2010, 105 (10) :2186-2194.
    [25] AZEMOTO N, KUMAGI T, ABE M, et al. Biochemical response to ursodeoxycholic acid predicts long-term outcome in Japanese patients with primary biliary cirrhosis[J]. Hepatol Res, 2011, 41 (4) :310-317.
    [26] LAMMERT C, JURAN B, SCHLICHT E, et al. Biochemical response to ursodeoxycholic acid predicts survival in a North American cohort of primary biliary cirrhosis patients[J]. J Gastroenterol, 2014, 49 (10) :1414-1420.
    [27] KUIPER EM, HANSEN BE, de VRIES RA, et al. Improved prognosis of patients with primary biliary cirrhosis that have a biochemical response to ursodeoxycholic acid[J]. Gastroenterology, 2009, 136 (4) :1281-1287.
    [28] HEGADE VS, KHANNA A, WALKER LJ, et al. Long-term fenofibrate treatment in primary biliary cholangitis improves biochemistry but not the UK-PBC risk score[J]. Digest Dis Sci, 2016, 61 (10) :3037-3044.
  • 期刊类型引用(13)

    1. 侯渌茗,陈逸云,张玮,李莹. 原发性胆汁性胆管炎的中西医治疗进展. 中国医刊. 2024(05): 478-481 . 百度学术
    2. 冯丽娜,张晓雪,黄剑洁,马博,温晓玉,陈满秋,金清龙. 原发性胆汁性胆管炎并发高脂血症的研究现状. 临床肝胆病杂志. 2021(01): 221-224 . 本站查看
    3. 杨宵,马丽,申慧琴. 原发性胆汁性胆管炎与调节性T细胞、吲哚胺2, 3-双加氧酶的相关性研究. 胃肠病学和肝病学杂志. 2021(03): 352-355 . 百度学术
    4. 李尧,徐晓欧. 自身免疫性肝病的发病机制及诊疗进展. 医学综述. 2021(09): 1707-1711 . 百度学术
    5. 李博云. 双歧杆菌三联活菌肠溶胶囊联合熊去氧胆酸治疗原发性胆汁性胆管炎患者效果观察. 华夏医学. 2021(04): 152-156 . 百度学术
    6. 王璐,韩英. 原发性胆汁性胆管炎的诊治现状与挑战. 临床肝胆病杂志. 2021(10): 2257-2261 . 本站查看
    7. 郝娟,吕靖,邢枫,杨全军,刘成海. 原发性胆汁性胆管炎的药物治疗进展. 临床肝胆病杂志. 2020(01): 222-226 . 本站查看
    8. 卫晶,武希润. 贝特类药物治疗原发性胆汁性胆管炎的研究现状. 临床肝胆病杂志. 2020(02): 442-445 . 本站查看
    9. 杨宁,刘雁声. 抗gp210抗体阳性原发性胆汁性胆管炎3例. 人民军医. 2020(07): 704-706+713 . 百度学术
    10. 郭风彩,吴剑明,卫峥. 对熊去氧胆酸应答不佳的原发性胆汁性胆管炎治疗策略分析. 临床医药文献电子杂志. 2020(50): 24+31 . 百度学术
    11. 刘晓,刘亚平,高学松,段雪飞. 原发性胆汁性胆管炎合并血脂异常研究进展. 中国肝脏病杂志(电子版). 2020(03): 17-22 . 百度学术
    12. 王璐,常英昊,韩英. 原发性胆汁性胆管炎的发病机制及治疗进展. 国际消化病杂志. 2019(02): 81-85 . 百度学术
    13. 易波,朱泽民,陈迅,赵志坚,唐才喜. 熊去氧胆酸治疗肝胆管结石行肝切除术后合并毛细胆管炎患者的临床疗效. 中国肝脏病杂志(电子版). 2019(04): 77-80 . 百度学术

    其他类型引用(10)

  • 加载中
计量
  • 文章访问数:  2362
  • HTML全文浏览量:  59
  • PDF下载量:  364
  • 被引次数: 23
出版历程
  • 出版日期:  2018-11-20
  • 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