• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

熊去氧胆酸用于原发性胆汁性肝硬化的长期治疗。

Prolonged treatment with ursodeoxycholic acid for primary biliary cirrhosis.

作者信息

Crippa G, Cagnoni C, Castelli A, Concesi C, Girometta S, Pancotti D, Sverzellati E, Tacchini G, Pierfranceschi M G, Carrara G C

机构信息

Department of Internal Medicine, Hospital, Piacenza.

出版信息

Clin Ter. 1995 May;146(5):367-72.

PMID:7796569
Abstract

Eighteen patients affected with biopsy-proved primary biliary cirrhosis (PBC) (histological stage III and IV) received ursodeoxicholic acid (UDCA) 600 mg for 1 year. Signs and symptoms and biochemical tests (glutamic and oxalcetic transaminase, glutamic and pyruvic transaminase, bilirubine, gamma-glutamyl transpeptidase, alkaline phosphatase, leucine aminopeptidase, bile acids, plasma proteins electrophoresis, immunoglubulins A, G and M) and antimitochondrial antibodies were evaluated before the treatment and every four months during the treatment. The results were compared with those obtained in 8 untreated patients affected PBC. The control group of patients were comparable (as far as age, histological stage, biochemical tests are concerned) to the group who received UDCA. Bilirubine, ALP, gamma-GT and LAP decreased during the treatment with UDCA and remained lower than baseline values until the end of the observation (12 months), while no changes occurred in the untreated patients. Both in the treated and untreated group plasma protein electrophoresis, serum immunoglubulins A, G and M remained unchanged, as well as anti-mitochondrial antibody. A moderate reduction of transaminases and bile acids was observed in the group of patients receiving UDCA but it did not reach statistical significance. In 16 out of the 18 treated patients pruritus disappeared and resulted diminished in the remaining 2 patients. No significant amelioration of pruritus was observed in the patients who did not receive UDCA. In conclusion, our data show that prolonged treatment with UDCA drastically reduces pruritus and improves cholestasis biochemical tests in patients affected with symptomatic PBC.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

18例经活检证实为原发性胆汁性肝硬化(PBC)(组织学分期为III期和IV期)的患者接受了600毫克熊去氧胆酸(UDCA)治疗,为期1年。在治疗前以及治疗期间每四个月对患者的体征和症状、生化检查(谷草转氨酶、谷丙转氨酶、胆红素、γ-谷氨酰转肽酶、碱性磷酸酶、亮氨酸氨基肽酶、胆汁酸、血浆蛋白电泳、免疫球蛋白A、G和M)以及抗线粒体抗体进行评估。将结果与8例未经治疗的PBC患者的结果进行比较。对照组患者在年龄、组织学分期、生化检查方面与接受UDCA治疗的组具有可比性。在使用UDCA治疗期间,胆红素、碱性磷酸酶、γ-谷氨酰转肽酶和亮氨酸氨基肽酶下降,并且在观察期结束(12个月)时仍低于基线值,而未经治疗的患者则无变化。在治疗组和未治疗组中,血浆蛋白电泳、血清免疫球蛋白A、G和M以及抗线粒体抗体均保持不变。在接受UDCA治疗的患者组中观察到转氨酶和胆汁酸有适度降低,但未达到统计学意义。18例接受治疗的患者中有16例瘙痒消失,其余2例患者瘙痒减轻。在未接受UDCA治疗的患者中未观察到瘙痒有明显改善。总之,我们的数据表明,UDCA的长期治疗可显著减轻有症状PBC患者的瘙痒,并改善胆汁淤积的生化检查结果。(摘要截选至250字)

相似文献

1
Prolonged treatment with ursodeoxycholic acid for primary biliary cirrhosis.熊去氧胆酸用于原发性胆汁性肝硬化的长期治疗。
Clin Ter. 1995 May;146(5):367-72.
2
Improvement of biliary enzyme levels and itching as a result of long-term administration of ursodeoxycholic acid in primary biliary cirrhosis.原发性胆汁性肝硬化患者长期服用熊去氧胆酸后胆汁酶水平及瘙痒症状的改善
Am J Gastroenterol. 1990 Jan;85(1):15-23.
3
[Efficacy of combined administration of ursodeoxycholic acid and hepthral in the treatment of primary biliary cirrhosis].熊去氧胆酸与肝得健联合应用治疗原发性胆汁性肝硬化的疗效
Klin Med (Mosk). 2004;82(3):55-8.
4
Methotrexate therapy for the symptomatic treatment of primary biliary cirrhosis patients, who are biochemical incomplete responders to ursodeoxycholic acid therapy.甲氨蝶呤用于对熊去氧胆酸治疗生化反应不完全的原发性胆汁性肝硬化患者进行症状性治疗。
Aliment Pharmacol Ther. 2006 Sep 1;24(5):813-20. doi: 10.1111/j.1365-2036.2006.03048.x.
5
Clinical and biochemical features and therapy responses in primary biliary cirrhosis and primary biliary cirrhosis-autoimmune hepatitis overlap syndrome.原发性胆汁性肝硬化及原发性胆汁性肝硬化-自身免疫性肝炎重叠综合征的临床、生化特征及治疗反应
Hepatogastroenterology. 2002 Sep-Oct;49(47):1195-200.
6
A randomized trial comparing colchicine and ursodeoxycholic acid combination to ursodeoxycholic acid in primary biliary cirrhosis. UDCA-PBC Study Group.一项比较秋水仙碱与熊去氧胆酸联合用药和熊去氧胆酸治疗原发性胆汁性肝硬化的随机试验。熊去氧胆酸治疗原发性胆汁性肝硬化研究组。
Hepatology. 1996 Nov;24(5):1098-103. doi: 10.1002/hep.510240520.
7
Primary biliary cirrhosis-autoimmune hepatitis overlap syndrome: clinical features and response to therapy.原发性胆汁性肝硬化-自身免疫性肝炎重叠综合征:临床特征及对治疗的反应
Hepatology. 1998 Aug;28(2):296-301. doi: 10.1002/hep.510280203.
8
The Canadian Multicenter Double-blind Randomized Controlled Trial of ursodeoxycholic acid in primary biliary cirrhosis.熊去氧胆酸治疗原发性胆汁性肝硬化的加拿大多中心双盲随机对照试验
Hepatology. 1994 May;19(5):1149-56.
9
Ursodeoxycholic acid treatment in primary biliary cirrhosis with the emphasis on late stage disease.熊去氧胆酸治疗原发性胆汁性肝硬化,重点关注晚期疾病。
Neth J Med. 1992 Aug;41(1-2):11-6.
10
Bezafibrate treatment: a new medical approach for PBC patients?苯扎贝特治疗:原发性胆汁性胆管炎患者的一种新的医学治疗方法?
J Gastroenterol. 2003;38(6):573-8. doi: 10.1007/s00535-002-1102-7.

引用本文的文献

1
Ursodeoxycholic acid for primary biliary cirrhosis.熊去氧胆酸用于原发性胆汁性肝硬化。
Cochrane Database Syst Rev. 2012 Dec 12;12(12):CD000551. doi: 10.1002/14651858.CD000551.pub3.
2
Drug therapy of primary biliary diseases: classical and modern strategies.原发性胆汁性疾病的药物治疗:经典与现代策略
J Cell Mol Med. 2001 Jan-Mar;5(1):98-115. doi: 10.1111/j.1582-4934.2001.tb00144.x.