期刊文献+

影响难治型原发性胆汁性肝硬化疗效的因素分析 被引量:3

Baseline analysis of refractory primary biliary cirrhosis
原文传递
导出
摘要 目的总结难治型原发性胆汁性肝硬化(PBC)的特点,比较其与典型PBC患者的异同,探索影响疗效的危险因素。方法对60例2009年8月至2011年5月北京协和医院随诊1年以上的PBC患者,根据对熊去氧胆酸(UDCA)应答情况,应答良好患者为典型组(37例),应答不良者为难治型组(23例),分析初治时两组临床资料的异同。结果难治型PBC患者初治时瘙痒(73.9%比45.9%)、乏力(60.9%比40.5%)、黄疸(43.4%比18.9%)发生率高于典型PBC患者(P〈0.05);难治型PBC患者在初治时有较高的血清丙氨酸氨基转移酶(ALT)、门冬氨酸氨基转移酶(AST)、碱性磷酸酶(ALP)、,y-谷氨酰转肽酶(GGT)、总胆红素(TBIL)和直接胆红素(DBIL)水平,且IgM高于典型组,而IgG较低(P〈0.05);难治型和典型PBC患者在年龄、性别、抗核抗体(ANA)、抗线粒体抗体(AMA)及M:亚型(AMA-M:)、其他相关抗体(如抗GP210、抗SPl00等)以及肝脏病理分期方面无统计学差异。结论初治时有瘙痒、乏力、黄疸等临床表现的,AlJrr、AST、ALP、GGT、TBIL和DBIL、IgM水平较高的PBC患者可能对UDCA应答不良。 Objective To summarize the clinical characters of refractory primary biliary cirrhosis (PBC) versus typical ones and explore the risk factors of prognosis. Methods From 2009 to 2011,60 PBC patients on the therapy of ursodeoxycholic acid (UDCA) over 1 year at our clinic were recruited. According to the response to UDCA by the Paris criteria, they were divided into refractory group ( n = 23 ) and typical group (n = 37) to analyze the basic clinical conditions, biochemical markers, antibodies and liver biopsies. Results (1) Compared with the typical patients, the refractory ones had more fatigue (73.9% vs 45.9%), pruritus (60.9% vs 40. 5%) and jaundice (43.4% vs 18. 9%); (2)the serum level of biomarkers ( alanine aminotransferase ( ALT), aspartate aminotransferase ( AST), alkaline phosphatase (ALP), ~/-glutamyl transpeptidase (GGT), total bilirubin (TBIL), direct bilirubin (DBIL) and immunoglobulin M ( IgM ) ) were higher in the refractory group ( P 〈 0. 05 ) ; ( 3 ) no differences existed between two groups in age, gender, antibodies ( antinuclear antibody ( ANA), antimitochondrial antibody (AMA), AMA-M2, anti-GP210, anti-SP100 and anti-centromere antibody (ACA) ) or liver biopsies. Conclusion Some clinical severe manifestation (fatigue, pruritus and jaundice) and higher biochemical markers levels (ALT, AST, ALP, GGT, TBIL, DBIL and IgM) seem to predict a worse response to UDCA and a rapid progression of disease in PBC patients.
出处 《中华医学杂志》 CAS CSCD 北大核心 2012年第41期2918-2920,共3页 National Medical Journal of China
基金 国家“十一五”科技支撑计划(2008BAl59803) 卫生部临床重点课题
关键词 肝硬化 胆汁性 碱性磷酸酶 Liver cirrhosis, biliary Alkaline phosphatase
  • 相关文献

参考文献8

  • 1Poupon R. Primary biliary cirrhosis: a 2010 update. J Hepatol, 2010, 52: 745-758.
  • 2Corpechot C, Abenacoli L, Rabahi N, et al. Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis. Hepatology, 2008, 48 : 871-877.
  • 3Lindor KD, Gershwin ME, Poupon R. Primary biliary cirrhosis. Hepatology, 2009, 50:291-308.
  • 4Scheuer PJ. Primary biliary cirrhosis: diagnosis, pathology and pathogenesis. Postgrad Med J, 1983, 59: 106-115.
  • 5A1-Harthy N, Kumagi T, Cohescu C, et 81. The specificity of fatigue in primary biliary cirrhosis: evaluation of a large clinic practice. Hepatology, 2010, 52: 562-570.
  • 6Jones DE, A1-Rifai A, Frith J, et al. The independent effects of fatigue and UDCA therapy on mortality in primary biliary cirrhosis: results of a 9 year follow-up . J Hepatol, 2010, 53: 911-917.
  • 7Ozaslan E, Efe C, Akbulut S, et al. Therapy response and outcome of overlap syndromes: autoimmune hepatitis and primary biliary cirrhosis compared to autoimmune hepatitis and autoimmune cholangitis. Hepatogastroenterology, 2010, 57 : 441- 446.
  • 8Agmon-Levin N, Shapira Y, Selmi C, et al. A comprehensive evaluation of serum autoantibodies in primary bihary cirrhosis. J Autoimmun, 2010, 34: 55-58.

同被引文献29

引证文献3

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部