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

被引:130
作者
Iwasaki, Shinji [1 ]
Ohira, Hiromasa [2 ]
Nishiguchi, Shuhei [3 ]
Zeniya, Mikio [4 ]
Kaneko, Shuichi [5 ]
Onji, Morikazu [6 ]
Ishibashi, Hiromi [7 ,8 ]
Sakaida, Isao [9 ]
Kuriyama, Shigeki [10 ]
Ichida, Takafumi [11 ]
Onishi, Saburo [1 ]
Toda, Gotaro [12 ]
机构
[1] Kochi Med Sch, Dept Gastroenterol & Hepatol, Nanko Ku, Kochi 7838505, Japan
[2] Fukushima Med Univ, Sch Med, Dept Internal Med 2, Fukushima, Japan
[3] Hyogo Coll Med, Div Hepatobiliary & Pancreat Med, Dept Internal Med, Nishinomiya, Hyogo, Japan
[4] Jikei Univ, Div Gastroenterol & Hepatol, Dept Internal Med, Sch Med, Tokyo, Japan
[5] Kanazawa Univ, Grad Sch Med Sci, Dept Dis Control & Homeostasis, Kanazawa, Ishikawa, Japan
[6] Ehime Univ, Grad Sch Med, Dept Gastroenterol & Metabol, Toon, Japan
[7] NHO Nagasaki Med Ctr, Dept Gen Internal Med, Omura, Japan
[8] NHO Nagasaki Med Ctr, Clin Res Ctr, Omura, Japan
[9] Yamaguchi Univ, Sch Med, Dept Gastroenterol & Hepatol, Ube, Yamaguchi 755, Japan
[10] Kagawa Univ, Fac Med, Dept Gastroenterol & Neurol, Kagawa, Japan
[11] Juntendo Univ, Sch Med, Shizuoka Hosp, Div Gastroenterol & Hepatol, Izunokuni, Japan
[12] Senpo Tokyo Takanawa Hosp, Tokyo, Japan
关键词
bezafibrate; primary biliary cirrhosis; ursodeoxycholic acid;
D O I
10.1111/j.1872-034X.2007.00305.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:557 / 564
页数:8
相关论文
共 22 条
[1]
Silymarin in the treatment of patients with primary biliary cirrhosis with a suboptimal response to ursodeoxycholic acid [J].
Angulo, P ;
Patel, T ;
Jorgensen, RA ;
Therneau, TM ;
Lindor, KD .
HEPATOLOGY, 2000, 32 (05) :897-900
[2]
Fibrates induce mdr2 gene expression and biliary phospholipid secretion in the mouse [J].
Chianale, J ;
Vollrath, V ;
Wielandt, AM ;
Amigo, L ;
Rigotti, A ;
Nervi, F ;
Gonzalez, S ;
Andrade, L ;
Pizarro, M ;
Accatino, L .
BIOCHEMICAL JOURNAL, 1996, 314 :781-786
[3]
Methotrexate (MTX) plus ursodeoxycholic acid (UDCA) in the treatment of primary biliary cirrhosis [J].
Combes, B ;
Emerson, SS ;
Flye, NL ;
Munoz, SJ ;
Luketic, VA ;
Mayo, MJ ;
McCashland, TM ;
Zetterman, RK ;
Peters, MG ;
Di Bisceglie, AM ;
Benner, KG ;
Kowdley, KV ;
Carithers, RL ;
Rosoff, L ;
Garcia-Tsao, G ;
Boyer, JL ;
Boyer, TD ;
Martinez, EJ ;
Bass, NM ;
Lake, JR ;
Barnes, DS ;
Bonacini, M ;
Lindsay, KL ;
Mills, AS ;
Markin, RS ;
Rubin, R ;
West, AB ;
Wheeler, DE ;
Contos, MJ ;
Hofmann, AF .
HEPATOLOGY, 2005, 42 (05) :1184-1193
[4]
Primary biliary cirrhosis: Incidence and predictive factors of cirrhosis development in ursodiol-treated patients [J].
Corpechot, C ;
Carrat, F ;
Poupon, R ;
Poupon, RE .
GASTROENTEROLOGY, 2002, 122 (03) :652-658
[5]
THE EFFECT OF BEZAFIBRATE TREATMENT ON SERUM ALKALINE-PHOSPHATASE ISOENZYME ACTIVITIES [J].
DAY, AP ;
FEHER, MD ;
CHOPRA, R ;
MAYNE, PD .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1993, 42 (07) :839-842
[6]
Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis [J].
De Vree, JML ;
Jacquemin, E ;
Sturm, E ;
Cresteil, D ;
Bosma, PJ ;
Aten, J ;
Deleuze, JF ;
Desrochers, M ;
Burdelski, M ;
Bernard, O ;
Elferink, RPJO ;
Hadchouel, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :282-287
[7]
Semiquantitation of intrahepatic MDR3 mRNA levels by reverse transcription competitive polymerase chain reaction [J].
Dumoulin, FL ;
Reichel, C ;
Sauerbruch, T ;
Spengler, U .
JOURNAL OF HEPATOLOGY, 1997, 26 (04) :852-856
[8]
Role of peroxisome proliferator-activated receptor-α (PPARα) in bezafibrate-induced hepatocarcinogenesis and cholestasis [J].
Hays, T ;
Rusyn, I ;
Burns, AM ;
Kennett, MJ ;
Ward, JM ;
Gonzalez, FJ ;
Peters, JM .
CARCINOGENESIS, 2005, 26 (01) :219-227
[9]
Farnesoid X receptor activates transcription of the phospholipid pump MDR3 [J].
Huang, L ;
Zhao, A ;
Lew, JL ;
Zhang, T ;
Hrywna, Y ;
Thompson, JR ;
de Pedro, N ;
Royo, I ;
Blevins, RA ;
Peláez, F ;
Wright, SD ;
Cui, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :51085-51090
[10]
Hepatoprotective bile acid 'ursodeoxycholic acid (UDCA)' Property and difference as bile acids [J].
Ishizaki, K ;
Imada, T ;
Tsurufuji, M .
HEPATOLOGY RESEARCH, 2005, 33 (02) :174-177