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非诺贝特是治疗原发性胆汁性肝硬化的有效辅助疗法:一项荟萃分析。

Fenofibrate is effective adjunctive therapy in the treatment of primary biliary cirrhosis: A meta-analysis.

作者信息

Grigorian Alla Y, Mardini Houssam E, Corpechot Christophe, Poupon Raoul, Levy Cynthia

机构信息

University of Kentucky College of Medicine, 800 Rose Street, Room MN649, Lexington, KY 40536, United States.

Service d'hépatologie, centre de référence des maladies inflammatoires des voies biliaires, hôpital Saint-Antoine, AP-HP, 75012 Paris, France; Inserm, UMR_S938, CDR Saint-Antoine, université Pierre-et-Marie-Curie Paris 6, 75012 Paris, France.

出版信息

Clin Res Hepatol Gastroenterol. 2015 Jun;39(3):296-306. doi: 10.1016/j.clinre.2015.02.011. Epub 2015 Apr 14.

Abstract

BACKGROUND AND AIM

Fenofibrate is a potential novel therapy for primary biliary cirrhosis (PBC). We performed a systematic review and a meta-analysis of studies of fenofibrate in PBC.

METHODS

Electronic database search was performed for relevant studies. A search of abstracts presented in the main scientific meetings in the field and articles in press was also performed. Random effect model was used to pool the effect size across studies for changes in alkaline phosphatase, GGT, bilirubin and IgM levels before and after treatment and the overall rate of complete response to fenofibrate therapy.

RESULTS

Six studies with 102 patients met the inclusion criteria. All studies were case series and in all, patients who had no or incomplete response to UDCA had fenofibrate added at a dose of 100-200mg daily. Treatment duration ranged from 8-100weeks. Treatment with fenofibrate was associated with a significant decrease in alkaline phosphatase (-114IU/L, 95% CI: -152 to -76, P<0.0001); a significant decrease in GGT level (-92IU/L, 95% CI: -149 to -43; P=0.0004); significant decrease in total bilirubin (-0.11mg/dL, 95% CI: -0.18 to -0.08; P=0.0008); and a significant decrease in IgM level (-88mg/dL, 95% CI: -119 to -58; P<0.0001). The complete response rate was 69% (95% CI: 53-82%) with an odds ratio of 82.8 (95% CI: 21.6-317.2; P=0.024) while on fenofibrate.

CONCLUSIONS

Fenofibrate at doses of 100-200mg daily appears to be effective adjunctive therapy in PBC patients who had no or incomplete response to UDCA. There is a critical need for larger scale randomized trials to determine its effect on liver-related morbidity and mortality (or progression towards end-stage disease).

摘要

背景与目的

非诺贝特是原发性胆汁性肝硬化(PBC)一种潜在的新型治疗方法。我们对非诺贝特治疗PBC的研究进行了系统评价和荟萃分析。

方法

对相关研究进行电子数据库检索。还检索了该领域主要科学会议上发表的摘要以及即将发表的文章。采用随机效应模型汇总各项研究中治疗前后碱性磷酸酶、γ-谷氨酰转肽酶(GGT)、胆红素和IgM水平变化的效应量以及非诺贝特治疗的完全缓解总率。

结果

6项研究共102例患者符合纳入标准。所有研究均为病例系列研究,总体而言,对熊去氧胆酸(UDCA)无反应或反应不完全的患者加用非诺贝特,剂量为每日100 - 200mg。治疗持续时间为8 - 100周。非诺贝特治疗与碱性磷酸酶显著降低(-114IU/L,95%CI:-152至-76,P<0.0001)、GGT水平显著降低(-92IU/L,95%CI:-149至-43;P = 0.0004)、总胆红素显著降低(-0.11mg/dL,95%CI:-0.18至-0.08;P = 0.0008)以及IgM水平显著降低(-88mg/dL,95%CI:-119至-58;P<0.0001)相关。非诺贝特治疗时完全缓解率为69%(95%CI:53 - 82%),优势比为82.8(95%CI:21.6 - 317.2;P = 0.024)。

结论

对于对UDCA无反应或反应不完全的PBC患者,每日剂量为100 - 200mg的非诺贝特似乎是有效的辅助治疗药物。迫切需要开展更大规模的随机试验以确定其对肝脏相关发病率和死亡率(或向终末期疾病进展)的影响。

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