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熊去氧胆酸联合苯扎贝特治疗原发性胆汁性肝硬化的疗效:一项前瞻性、多中心研究。

The efficacy of ursodeoxycholic acid and bezafibrate combination therapy for primary biliary cirrhosis: A prospective, multicenter study.

机构信息

Department of Gastroenterology and Hepatology, Kochi Medical School, Kochi, Japan.

出版信息

Hepatol Res. 2008 Jun;38(6):557-64. doi: 10.1111/j.1872-034X.2007.00305.x.

Abstract

AIM

Treatment with ursodeoxycholic acid (UDCA) improves the survival of stage I and II primary biliary cirrhosis (PBC) patients. However, new therapeutic options are needed for patients who are refractory to UDCA and for those whose disease is at an advanced stage. Bezafibrate could be useful in PBC treatment, since it increases phospholipid output into the bile and reduces the cytotoxicity of hydrophobic bile acids, which are increased with cholestasis.

METHODS

We conducted two prospective, multicenter randomized open studies in non-cirrhotic patients with PBC to evaluate the efficacy of bezafibrate. One study compared UDCA and bezafibrate monotherapy (study 1: 45 patients [37 females], mean age 55.9 years), and the other evaluated the addition of bezafibrate to patients who were refractory to UDCA (study 2: 21 patients [18 females], mean age 54.1 years).

RESULTS

Study 1 demonstrated that bezafibrate monotherapy was as effective as UDCA and study 2 revealed that bezafibrate combined with UDCA was effective in improving and maintaining biliary enzymes where the ineffectiveness of long-term treatment with UDCA was confirmed.

CONCLUSION

This multicenter, randomized, open study revealed that combination therapy of bezafibrate and UDCA improved biliary enzymes in non-cirrhotic Japanese patients with PBC refractory to UDCA. Further studies are needed to evaluate whether combination therapy improves histological staging and prognosis.

摘要

目的

熊去氧胆酸(UDCA)的治疗可改善 I 期和 II 期原发性胆汁性肝硬化(PBC)患者的生存率。然而,对于 UDCA 耐药的患者和疾病处于晚期的患者,需要新的治疗选择。非诺贝特可能对 PBC 的治疗有用,因为它增加了磷脂向胆汁中的输出,并减少了疏水性胆汁酸的细胞毒性,疏水性胆汁酸在胆汁淤积时会增加。

方法

我们在非肝硬化 PBC 患者中进行了两项前瞻性、多中心、开放性随机研究,以评估非诺贝特的疗效。一项研究比较了 UDCA 和非诺贝特单药治疗(研究 1:45 例患者[37 例女性],平均年龄 55.9 岁),另一项研究评估了非诺贝特在 UDCA 耐药患者中的添加治疗(研究 2:21 例患者[18 例女性],平均年龄 54.1 岁)。

结果

研究 1 表明,非诺贝特单药治疗与 UDCA 一样有效,研究 2 表明,非诺贝特联合 UDCA 可有效改善和维持胆汁酶,证实了长期 UDCA 治疗无效。

结论

这项多中心、随机、开放性研究表明,非诺贝特联合 UDCA 治疗可改善对 UDCA 耐药的日本非肝硬化 PBC 患者的胆汁酶。需要进一步研究来评估联合治疗是否改善组织学分期和预后。

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