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熊去氧胆酸、泼尼松和硫唑嘌呤三联疗法治疗原发性胆汁性肝硬化:一项为期1年的随机、安慰剂对照研究。

Triple therapy with ursodeoxycholic acid, prednisone and azathioprine in primary biliary cirrhosis: a 1-year randomized, placebo-controlled study.

作者信息

Wolfhagen F H, van Hoogstraten H J, van Buuren H R, van Berge-Henegouwen G P, ten Kate F J, Hop W C, van der Hoek E W, Kerbert M J, van Lijf H H, den Ouden J W, Smit A M, de Vries R A, van Zanten R A, Schalm S W

机构信息

Department of Hepatogastroenterology, University Hospital Rotterdam, The Netherlands.

出版信息

J Hepatol. 1998 Nov;29(5):736-42. doi: 10.1016/s0168-8278(98)80254-7.

Abstract

BACKGROUND/AIMS: Treatment with ursodeoxycholic acid has been shown to decrease the rate of disease progression in patients with primary biliary cirrhosis, although the effect is modest. Since primary biliary cirrhosis has many features of an autoimmune disorder, immunosuppressives added to ursodeoxycholic acid may be of value in the treatment of primary biliary cirrhosis.

METHODS

A 1-year randomized, double-blind, placebo-controlled trial was carried out in 50 patients with primary biliary cirrhosis, who had already been treated with ursodeoxycholic acid for at least 1 year, but had not achieved complete disease remission. Patients were randomized to additional prednisone (30 mg per day initially, tapered to 10 mg daily after 8 weeks) and azathioprine (50 mg daily) or placebo. A subgroup of patients received cyclical etidronate and calcium. The principal aim of the study was to assess the short-term benefits and risks of the combined bile acid and low-dose immunosuppressive regimen. Primary endpoints were effects on symptoms, liver biochemistry, liver histology, bone mass and the occurrence of adverse events.

RESULTS

Pruritus (p=0.02), alkaline phosphatase, aspartate aminotransferase, IgM and procollagen-III-propeptide improved significantly (all p<0.002) in the combined treatment group as compared to the placebo group. Histological scores for disease activity and disease stage decreased significantly within the combination treatment group (p<0.001).

CONCLUSIONS

In patients with primary biliary cirrhosis receiving ursodeoxycholic acid, there is an additional beneficial effect of 1-year treatment with prednisone and azathioprine on symptoms and biochemical, fibrogenetic and histological parameters. These results strongly encourage the evaluation of this triple treatment regimen in long-term controlled trials of adequate size to document its effect on clinical events.

摘要

背景/目的:已表明用熊去氧胆酸治疗可降低原发性胆汁性肝硬化患者的疾病进展速率,尽管效果不显著。由于原发性胆汁性肝硬化具有自身免疫性疾病的许多特征,在熊去氧胆酸基础上加用免疫抑制剂可能对原发性胆汁性肝硬化的治疗有价值。

方法

对50例原发性胆汁性肝硬化患者进行了一项为期1年的随机、双盲、安慰剂对照试验,这些患者已接受熊去氧胆酸治疗至少1年,但疾病未完全缓解。患者被随机分配接受额外的泼尼松(初始每日30mg,8周后减至每日10mg)和硫唑嘌呤(每日50mg)或安慰剂。一组亚组患者接受周期性依替膦酸和钙剂治疗。该研究的主要目的是评估联合胆汁酸和低剂量免疫抑制方案的短期益处和风险。主要终点是对症状、肝脏生化指标、肝脏组织学、骨量和不良事件发生情况的影响。

结果

与安慰剂组相比,联合治疗组的瘙痒(p=0.02)、碱性磷酸酶、天冬氨酸转氨酶、IgM和前胶原III前肽均有显著改善(均p<0.002)。联合治疗组内疾病活动度和疾病分期的组织学评分显著降低(p<0.001)。

结论

在接受熊去氧胆酸治疗的原发性胆汁性肝硬化患者中,泼尼松和硫唑嘌呤1年治疗对症状以及生化、纤维生成和组织学参数有额外的有益作用。这些结果强烈鼓励在足够规模的长期对照试验中评估这种三联治疗方案,以记录其对临床事件的影响。

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