Serum MMP-3 Level as a Biomarker for Monitoring and Predicting Response to Etanercept Treatment in Ankylosing Spondylitis

被引:45
作者
Arends, Suzanne [1 ]
van der Veer, Eveline [2 ]
Groen, Henk [3 ]
Houtman, Pieternella M.
Jansen, Tim L. T. A. [4 ]
Leijsma, Martha K. [1 ]
Bijzet, Johan [1 ]
Limburg, Pieter C. [1 ,2 ]
Kallenberg, Cees G. M. [1 ]
Spoorenberg, Anneke [4 ]
Brouwer, Elisabeth [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Rheumatol & Clin Immunol, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Lab Med, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, NL-9700 RB Groningen, Netherlands
[4] Med Ctr Leeuwarden, Dept Rheumatol, Leeuwarden, Netherlands
关键词
ANKYLOSING SPONDYLITIS; SERUM MMP-3 LEVELS; BIOMARKERS; PREDICTORS; ETANERCEPT TREATMENT; ERYTHROCYTE SEDIMENTATION-RATE; NECROSIS-FACTOR-ALPHA; C-REACTIVE PROTEIN; MATRIX-METALLOPROTEINASE EXPRESSION; EARLY RHEUMATOID-ARTHRITIS; DISEASE-ACTIVITY; STRUCTURAL DAMAGE; TRIAL; MATRIX-METALLOPROTEINASE-3; DESTRUCTION;
D O I
10.3899/jrheum.101128
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective. To investigate whether level of serum matrix metalloproteinase-3 (MMP-3) can serve as a biomarker for monitoring and predicting response to etanercept treatment in patients with ankylosing spondylitis (AS) in daily clinical practice. Methods. Ninety-two consecutive AS outpatients with active disease who started etanercept treatment were included in this longitudinal observational study. Clinical data were collected prospectively at baseline and after 3 and 12 months of treatment. At the same timepoints, serum MMP-3 levels were measured retrospectively by ELISA. Results. Since baseline serum MMP-3 levels were significantly higher in male compared to female patients with AS, data analysis was split for gender. Changes in serum MMP-3 levels after etanercept treatment correlated positively with changes in clinical assessments of disease activity and physical function in both male and female patients. Receiver operating characteristic analysis in male patients showed that baseline serum MMP-3 levels had poor accuracy (AUC < 0.7) to discriminate between Assessments in Ankylosing Spondylitis 20 (ASAS20) or ASAS40 responders and nonresponders after 3 or 12 months of treatment. The accuracy of change in serum MMP-3 levels from baseline to 3 months in predicting response after 3 or 12 months of treatment was poor for ASAS40 (AUC < 0.7) or moderate for ASAS20 (AUC = 0.752 and 0.744, respectively), and was not superior to the accuracy of change in the currently used objective biomarkers, erythrocyte sedimentation rate and C-reactive protein. Conclusion. Although significant changes in serum MMP-3 levels were found after etanercept treatment, data analysis indicates that serum MMP-3 levels are not very useful for monitoring and predicting response to etanercept treatment in patients with AS in daily clinical practice. (First Release June 1 2011; J Rheumatol 2011;38:1644-50; doi :10.3899/jrheum.101128)
引用
收藏
页码:1644 / 1650
页数:7
相关论文
共 35 条
[1]
Appel H, 2009, ANN RHEUM DIS S, V68, P641
[2]
Serum levels of biomarkers of bone and cartilage destruction and new bone formation in different cohorts of patients with axial spondyloarthritis with and without tumor necrosis factor-alpha blocker treatment [J].
Appel, Heiner ;
Janssen, Louise ;
Listing, Joachim ;
Heydrich, Rene ;
Rudwaleit, Martin ;
Sieper, Joachim .
ARTHRITIS RESEARCH & THERAPY, 2008, 10 (05)
[3]
ARENDS S, 2010, OSTEOPOROS INT 0706
[4]
First update of the international ASAS consensus statement for the use of anti-TNF agents in patients with ankylosing spondylitis [J].
Braun, J ;
Davis, J ;
Dougados, M ;
Sieper, J ;
van der Linden, S ;
van der Heijde, D .
ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (03) :316-320
[5]
Ankylosing spondylitis [J].
Braun, Juergen ;
Sieper, Joachim .
LANCET, 2007, 369 (9570) :1379-1390
[6]
Outcomes of a multicentre randomised clinical trial of etanercept to treat ankylosing spondylitis [J].
Calin, A ;
Dijkmans, BAC ;
Emery, P ;
Hakala, M ;
Kalden, J ;
Leirisalo-Repo, M ;
Mola, EM ;
Salvarani, C ;
Sanmartí, R ;
Sany, J ;
Sibilia, J ;
Sieper, J ;
van der Linden, S ;
Veys, E ;
Appel, AM ;
Fatenejad, S .
ANNALS OF THE RHEUMATIC DISEASES, 2004, 63 (12) :1594-1600
[7]
CALIN A, 1994, J RHEUMATOL, V21, P2281
[8]
Serum matrix metalloproteinases and tissue inhibitors of metalloproteinases in ankylosing spondylitis: MMP-3 is a reproducibly sensitive and specific biomarker of disease activity [J].
Chen, CH ;
Lin, KC ;
Yu, DTY ;
Yang, C ;
Huang, F ;
Chen, HA ;
Liang, TH ;
Liao, HT ;
Tsai, CY ;
Wei, JCC ;
Chou, CT .
RHEUMATOLOGY, 2006, 45 (04) :414-420
[9]
Erythrocyte Sedimentation Rate, C-Reactive Protein Level, and Serum Amyloid A Protein for Patient Selection and Monitoring of Anti-Tumor Necrosis Factor Treatment in Ankylosing Spondylitis [J].
de Vries, Mirjam K. ;
van Eijk, Izhar C. ;
van der Horst-Bruinsma, Irene E. ;
Peters, Mike J. L. ;
Nurmohamed, Michael T. ;
Dijkmans, Ben A. C. ;
Hazenberg, Bouke P. C. ;
Wolbink, Gerrit J. .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2009, 61 (11) :1484-1490
[10]
GARRETT S, 1994, J RHEUMATOL, V21, P2286