A meta-analysis of the role of p38 mitogen-activated protein kinase inhibitors in patients with active rheumatoid arthritis

被引:9
作者
Li, Lan [1 ]
Li, Guogang [2 ]
Yu, Chaohui [1 ]
Li, Youming [1 ]
机构
[1] Zhejiang Univ, Coll Med, Affiliated Hosp 1, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Univ, Coll Med, Affiliated Hosp 2, Hangzhou 310009, Zhejiang, Peoples R China
关键词
Meta-analysis; p38 Mitogen-activated protein kinase inhibitors; Rheumatoid arthritis; DOUBLE-BLIND; MAPK INHIBITOR; EFFICACY; PAMAPIMOD; PHARMACODYNAMICS; METHOTREXATE; SCIO-469; SAFETY;
D O I
10.1007/s10067-013-2340-1
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The role of p38 mitogen-activated protein kinase (MAPK) inhibitors for treating rheumatoid arthritis (RA) is debated. Therefore, we performed a meta-analysis of all published randomized controlled trials (RCTs) to evaluate the efficacy and safety of p38 MAPK inhibitors in patients with active RA. Searches were conducted in the databases PubMed, EMBASE, and Cochrane Library. We identified three articles including four RCTs with analysis on the efficacy and safety of p38 inhibitors for the treatment of RA. Our meta-analysis showed that a better American College of Rheumatology 20 % improvement (ACR20) was observed in the p38 inhibitors group compared with the placebo group, but there were no meaningful differences in ACR50, Disease Activity Score in 28 joints response, and CRP levels between two groups past week 12. The overall adverse events were similar between placebo and treatment groups. In conclusion, p38 MAPK inhibitors showed modest efficacy in patients with RA. However, this conclusion is based on the small number of available studies and inadequate sample size, and more well-designed RCTs will be necessary to determine the role of p38 MAPK inhibitors in RA.
引用
收藏
页码:1697 / 1702
页数:6
相关论文
共 19 条
[11]
A PROTEIN-KINASE INVOLVED IN THE REGULATION OF INFLAMMATORY CYTOKINE BIOSYNTHESIS [J].
LEE, JC ;
LAYDON, JT ;
MCDONNELL, PC ;
GALLAGHER, TF ;
KUMAR, S ;
GREEN, D ;
MCNULTY, D ;
BLUMENTHAL, MJ ;
HEYS, JR ;
LANDVATTER, SW ;
STRICKLER, JE ;
MCLAUGHLIN, MM ;
SIEMENS, IR ;
FISHER, SM ;
LIVI, GP ;
WHITE, JR ;
ADAMS, JL ;
YOUNG, PR .
NATURE, 1994, 372 (6508) :739-746
[12]
Pro-inflammatory cytokine-induced SAPK/MAPK and JAK/STAT in rheumatoid arthritis and the new anti-depression drugs [J].
Malemud, Charles J. ;
Miller, Andrew H. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2008, 12 (02) :171-183
[13]
Prevention of the onset and progression of collagen-induced arthritis in rats by the potent p38 mitogen-activated protein kinase inhibitor FR167653 [J].
Nishikawa, M ;
Myoui, A ;
Tomita, T ;
Takahi, K ;
Nampei, A ;
Yoshikawa, H .
ARTHRITIS AND RHEUMATISM, 2003, 48 (09) :2670-2681
[14]
Oral p38 mitogen-activated protein kinase inhibition with BIRB 796 for active Crohn's disease: A randomized, double-blind, placebo-controlled trial [J].
Schreiber, S ;
Feagan, B ;
D'Haens, G ;
Colombel, JF ;
Geboes, K ;
Yurcov, M ;
Isakov, V ;
Golovenko, O ;
Bernstein, CN ;
Ludwig, D ;
Winter, T ;
Meier, U ;
Yong, C ;
Steffgen, J .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2006, 4 (03) :325-334
[15]
Thalhamer T, 2008, RHEUMATOLOGY, V47, P409, DOI 10.1093/rheumatology/kem297
[16]
SCIO-469, a novel p38a MAPK inhibitor, provides efficacy in acute post-surgical dental pain. [J].
Tong, SE ;
Daniels, SE ;
Montano, T ;
Chang, S ;
Desjardins, P .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2004, 75 (02) :P3-P3
[17]
Pre-ERCP infusion of semapimod, a mitogen-activated protein kinases inhibitor, lowers post-ERCP hyperamylasemia but not pancreatitis incidence [J].
van Westerloo, David J. ;
Rauws, Erik A. ;
Hommes, Daan ;
de Vos, Alex F. ;
van der Poll, Tom ;
Powers, Barbara L. ;
Fockens, Paul ;
Dijkgraaf, Marcel G. W. ;
Bruno, Marco J. .
GASTROINTESTINAL ENDOSCOPY, 2008, 68 (02) :246-254
[18]
Weisman M, 2002, 2002 ANN EUR C RHEUM
[19]
A Proof-of-Concept and Drug-Drug Interaction Study of Pamapimod, a Novel p38 MAP Kinase Inhibitor, With Methotrexate in Patients With Rheumatoid Arthritis [J].
Zhang, Xiaoping ;
Huang, Yue ;
Navarro, Mercidita T. ;
Hisoire, Grace ;
Caulfield, John P. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2010, 50 (09) :1031-1038