- Research article
- Open Access
Association of circulating levels of MMP-8 with mortality from respiratory disease in patients with rheumatoid arthritis
Arthritis Research & Therapy volume 14, Article number: R204 (2012)
Matrix metalloproteinases (MMPs) are implicated in the destruction of the joint and have been shown to be strongly associated with inflammation in rheumatoid arthritis (RA). Circulating MMPs have also been associated with cardiovascular disease in the general population, and are predictive of cardiovascular mortality. The purpose of the present study was to determine whether circulating levels of MMPs are predictive of mortality in RA.
A multiplex suspension array system (Luminex®) was used to measure levels of MMPs (1, 2, 3, 8 and 9) in sera taken at recruitment of RA patients (n = 487) in a study of factors associated with mortality in RA. Patients were tracked on the National Health Service Central Register for notification of death, and the relationship between baseline MMP levels and mortality was analysed using Cox proportional hazards regression analysis.
At the time of follow-up, 204/486 patients had died, of which 94 (46.1%) had died of circulatory diseases, 49 of malignancy (24.0%), and 42 (20.6%) of respiratory diseases. In a stepwise analysis which included all MMPs, only MMP-8 was significantly associated with all cause mortality (P = 0.0007, 0.6% hazard ratio increase per ng/ml). No association was found between MMP levels and mortality due to circulatory disease or malignancy. However MMP-8 levels were strongly associated with mortality due to respiratory disease (P < 0.0001, 1.3% hazard ratio increase per ng/ml). The association with respiratory disease related mortality remained highly significant in multivariate models which included smoking as well as markers of severity and disease activity such as rheumatoid factor, nodular disease, and C-reactive protein (CRP).
The serum level of MMP-8 is a strong predictor of mortality in RA, especially that due to respiratory disease. This finding is consistent with increased activation of neutrophils in RA and identifies serum MMP-8 as a useful marker for increased risk of premature death.
Many studies have shown that the mortality rate is increased in patients with rheumatoid arthritis (RA) compared with the general population [1–6]. Causes of death in RA are similar to those in the general population but there is an increased risk of death due to cardiovascular disease (CVD), and an excess of deaths due to infection, much of which is due to lower respiratory tract infections [1, 2, 7–12].
Markers of inflammation such as erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) and soluble tumour necrosis factor receptors have been shown to be predictive of mortality in RA [2, 3, 5, 7–9, 13], but many other markers associated with the disease process have not been investigated. Some of these may provide alternative or better predictors of early mortality. One such group of markers are the matrix metalloproteinases (MMPs). These are implicated in the destruction of the joint and have been shown to be strongly associated with inflammation and disease activity in RA [14–18]. Circulating MMPs have also been associated with CVD and atherosclerotic plaque instability in non-RA patients [19–25], and have been shown to be predictive of cardiovascular mortality [20, 25].
We postulated that elevated levels of circulating MMPs in RA patients may be associated not only with increased rheumatoid disease activity and severity, but may also predict premature mortality. We have thus investigated the relationship of circulating levels of MMPs with all-cause, and cause-specific mortality, and determined whether any relationship between mortality and MMP levels was independent of traditional risk factors and other markers of inflammation and disease severity.
Materials and methods
This was a follow up study of a cohort of RA patients from North Staffordshire, England, recruited between 1993 and 1998 to investigate long-term outcome and mortality in patients attending a hospital-based clinic at the Haywood Rheumatology Centre. Consecutive cases were selected from clinics of confirmed RA patients who satisfied the 1987 American College of Rheumatology criteria for RA . Baseline assessments included the disability index of the Stanford health assessment questionnaire (HAQ) , presence of erosions, CRP and ESR levels, IgM rheumatoid factor (RF), and presence or absence of nodular disease. Age, sex, disease duration at recruitment, and history of current or past cigarette smoking was also recorded. As an indication of pre-existing CVD at the time of recruitment, patients were stratified according to whether or not they were taking any drugs for cardiovascular problems. This included patients taking drugs for cardiac and non-cardiac conditions, the latter including cerebrovascular disease and peripheral vascular disease. Patients taking drugs for hypertension alone were not included in this group. The study was approved by the North Staffordshire local research ethics committee.
The treatment of patients at baseline reflected standard UK practice for management of hospital-based RA patients as outlined in published guidelines . Patients were receiving anti-inflammatory and/or anti-rheumatic therapy, with the majority of patients (> 90%) being treated with one or more disease modifying anti-rheumatic drugs (DMARDs). DMARDs were chosen according to physician's preference, using the standard practice at the time of sequential monotherapy and combination therapy for more severe disease. The most common combination was methotrexate and sulphasalazine. Steroids and cytotoxic drugs such as azathioprine or cyclophosphamide were received by a small minority of individuals (< 5%). A number of patients (8%) were treated with anti-TNF agents during the latter years of the study (from 2002). These patients all fulfilled the United Kingdom National Institute of Clinical Excellence (NICE) criteria for use of anti-TNF therapy.
Survival follow up
All patients were registered on the NHS Central Register (NHSCR), a computerised registry of the records of all patients registered with a general practitioner in England and Wales. Access to this registry was obtained via the Office for National Statistics (ONS), General Register Office, Southport, UK. Patients were tracked on the NHSCR, and notification of patient deaths was obtained from the ONS within 1 month of death. Causes of death were coded by the ONS, using the International Classification of Diseases Ninth Revision (ICD-9)  up until 31 December 2000, and ICD-10 after this date. Patients were followed up to 31 December 2011.
Multiplex MMP assays
Sera were separated from bloods collected in plain glass Becton Dickinson (BD) (Becton Dickinson, Oxford, Oxfordshire, UK) Vacutainer® tubes at study entry. Bloods were allowed to clot for 60 minutes at room temperature before serum separation and storage at -70o C until required. Measurement of MMP-1, 2, 3, 8 and 9 levels was performed on the serum samples using Fluorokine MAP multiplex kits (R&D Systems, Minneapolis, MN, USA) and was read on a Luminex® suspension array system (Bio-Plex 200™, Bio-Rad (Bio-Rad Laboratories, Hemel Hempstead, Hertfordshire, UK)). Sample preparation and assay procedure were followed according to the manufacturer's recommendation. Heteroblock (Omega Biologicals, Bozeman, MT, USA) was added at a concentration of 150 ug/ml into the sample diluent prior to assay, to block any non-specific binding to RF . All samples were run in duplicate with the appropriate standards on 96-well microplates. The limit of detection for each of the MMPs was as follows: MMP-1, 0.04 ng/ml; MMP-2, 0.03 ng/ml; MMP-3, 0.01 ng/ml; MMP-8, 0.04 ng/ml; MMP-9, 0.74 ng/ml. The intra- and inter-assay coefficients of variation for each of the MMPs were between 1.5 and 9.2%, and 6.2 and 15.2% respectively.
Spearman's rank correlation was used to assess the relationship between MMP levels and measures of disease activity and severity. The Mann-Whitney U-test was used to determine baseline differences in MMP levels between patients with and without nodular or erosive disease, between smokers and non-smokers and between surviving and non-surviving patients. The association between serum MMP levels and mortality risk was investigated using Cox proportional hazard regression analyses adjusted for age, sex and disease duration at baseline. The time intervals for those patients who were alive at the end of the study period and those who were lost to follow up were censored. The censoring date was the date of the last hospital visit. Since mortality data are recorded centrally in the UK, we were able to collect mortality data on all patients entered into the study, and patients lost to follow up without a documented death could be censored with some degree of certainty. Multivariate stepwise models were used to assess the predictive value of MMP levels compared with other potential baseline risk factors (such as, RF, nodules, CRP, ESR, HAQ, taking CVD drugs, smoking status). Separate analyses were carried out on the risk of mortality related to each of the major causes of death in RA, namely circulatory, malignant and respiratory diseases. In these analyses the data on subjects who died of other causes, and the data on those who were still alive at last follow up were censored.
Kaplan-Meier curves were plotted to illustrate survival in relation to median MMP levels at baseline. All data were analysed using Number Cruncher Statistical Software package for Windows (NCSS 2000, NCSS Statistical Software, Kaysville, UT, USA), and GraphPad Prism software (version 1.03, GraphPad Software Incorporated, San Diego, CA, USA).
Characteristics of RA patients
The baseline clinical features of the cohort are summarised in Table 1. Of the 487 patients recruited there were 204 deaths (41.9%), of which 86 were men and 118 were women. For patients who died the median survival time from study baseline was 6.9 years (interquartile range (IQR) 3.6 to 12.1). For survivors the median follow up period from baseline was 16.2 years (IQR 5.9 to 17.2).
Main causes of death
The three major causes of death were due to circulatory disease (94/204, 46.1%), neoplasia (49/204, 24.0%) and respiratory diseases (42/204, 20.6%). Of the 94 patients who died from circulatory disease, 62 were due to heart disease (mainly ischaemic heart disease, congestive heart failure, or left ventricular failure), and 19 were due to cerebrovascular disease. The main cause of respiratory disease related mortality was pneumonia (29/42). In this group, pneumonia was recorded as the only cause of death, or the only cause with RA as a contributing cause in 23/29 patients. Of the remaining six patients with pneumonia, three also had longstanding chronic obstructive pulmonary disease (COPD), one had pulmonary fibrosis, one had CVD and one was associated with sepsis.
Relationship between MMP levels and patient characteristics at baseline
There was a positive correlation between the levels of all the MMPs apart from MMP-2 (Additional file 1). Comparison of MMP levels in men and women showed a significantly higher median level of MMP-3 (28.1 v 21.2 ng/ml, P = 0.00008), MMP-8 (23.37 v 17.96 ng/ml, P = 0.0008) and MMP-9 (435.5 v 363.5 ng/ml, P = 0.001) in men. The levels of MMP-1, MMP-2 and MMP-3 showed a significant increase with age (Rs ≥ 0.106, P ≤ 0.01), independent of disease duration (Additional file 2). Most measures of disease activity and severity (ESR, CRP, HAQ, Larsen score, visual analogue (VAS) pain score) were positively correlated with levels of all MMPs apart from MMP-2 (Additional file 2). The latter showed a negative correlation with CRP and the VAS pain score. No correlation was found between IgM RF titres and MMP levels. Patients with erosive disease had significantly higher levels of MMP-3 than those with non-erosive disease (25.46 v 15.35 ng/ml, P = 0.006), but no difference was found for other MMPs. The association with MMP-3 remained significant after adjusting for age, sex and disease duration (data not shown). No difference in MMP levels was found between patients with or without nodular disease. Patients who were taking one or more drugs for CVD at baseline had significantly higher levels of MMP-2, MMP-8 and MMP-9 than patients not taking these drugs (146.3 v 131.1 ng/ml, P = 0.007, 26.67 v 20.32 ng/ml, P = 0.02, and 471.5 v 413.7, P = 0.049 respectively). However, in a stepwise analysis adjusted for age, sex and disease duration, there was only an association with MMP-9 levels (data not shown). Patients that had ever smoked also had higher levels of MMP-8 and MMP-9 than those who had never smoked (22.05 v 17.46 ng/ml, P = 0.015, and 411.2 v 344.8 ng/ml, P = 0.004 respectively).
Relationship between MMP levels and mortality
Compared with surviving patients, baseline levels of MMP-2 were significantly higher in patients who died during follow up (Table 2). Stratification by causes of death also demonstrated that higher levels of MMP-2 were found in patients who later died from circulatory disease, but higher levels of MMP-8 were found in patients who died from respiratory disease. Baseline MMP-1 levels were lower in patients who later died from malignant disease, but this association disappeared after adjusting for age, sex and disease duration (data not shown). The association of high baseline MMP-2 levels with patients who later died also disappeared after adjusting for age, sex and disease duration. However, the association of high MMP-8 levels with patients later dying of respiratory disease remained after such adjustment (P = 0.01).
We next investigated whether the mortality risk increased with increasing levels of MMPs. Separate Cox analysis for each MMP, with adjustment for age, sex and disease duration demonstrated significant increases in the hazard ratio (HR) with increasing levels of MMP-8 and MMP-9 (Table 3). No association with MMP-2 levels was seen in Cox models adjusted for age. Analyses of cause-specific mortality demonstrated significant associations of MMP-8 and MMP-9 with mortality due to respiratory disease (Table 4). No associations were found with any MMPs for deaths due to circulatory disease or neoplasia.
Multivariate survival analysis
In stepwise Cox proportional hazards regression models that included all MMPs, only MMP-8 was found to be significantly associated with all-cause mortality (HR = 1.006 per ng/ml, 95% CI 1.002, 1.01, P = 0.003). Further multivariate analyses including other risk factors revealed that MMP-8 level was predictive of mortality independently of age, smoking at baseline, nodular disease, and taking CVD drugs at baseline, all of which were associated with all-cause mortality (Table 5). Other disease activity and severity markers (CRP, ESR, HAQ, RF, Larsen score) were excluded due to non-significance in stepwise analysis (Table 5).
Mortality due to circulatory diseases was not associated with levels of any MMP, although when mortality due to heart disease alone was analysed a significant association with baseline MMP-9 levels was found (HR 1.0013 per ng/ml, P = 0.01). This remained significant (P = 0.01) after adjusting for smoking at baseline and nodular disease, but significance was lost when adjusted for patients taking CVD drugs at baseline. The latter association was highly significant (HR 4.60, 95% CI 2.39, 8.94, P < 0.0001). As in the case of all-cause mortality, we found that age, smoking at baseline and nodular disease were all significantly associated, with or without adjustment for taking CVD drugs.
Mortality due to neoplasia was not associated with levels of any MMP. The most significant predictors were older age, and smoking at baseline (data not shown). Multivariate analysis of mortality due to respiratory disease showed that MMP-8 level was a highly significant predictor along with age, nodular disease and presence of RF (Table 5). Although significant in univariate analysis, MMP-9 levels were not significantly associated in a model that also included MMP-8 levels. Smoking and measures of inflammation were not associated. Separate analyses of patients who had died from pneumonia or from other causes of respiratory disease demonstrated a significant association with MMP-8 levels in both cases, although the number of patients who had died from causes other than pneumonia was small (n = 13) (Table 6).
Figure 1 illustrates the survival of patients in relation to the median cutoff level for MMP-8 (20.07 ng/ml) at baseline using Kaplan-Meier analysis to generate survival curves based on mortality due to respiratory disease (Figure 1A) or pneumonia alone (Figure 1B). Levels equal to and above the median were associated with significantly worse survival (HR 2.63, 95% CI 1.38, 5.05, P = 0.003 and HR 4.44, 95% CI 1.86, 10.59, P = 0.0007 respectively, after adjustment for age, sex and disease duration at baseline).
Our data indicate that the serum level of MMP-8 (neutrophil collagenase) is a strong predictor of mortality in RA, especially that due to respiratory disease. As far as we are aware, this is the first study to identify a biomarker that is predictive of respiratory disease-related mortality in RA. Age, nodular disease and presence of RF were also predictive but the MMP-8 association was independent of these. Although the majority of deaths in this group of patients were due to pneumonia, separate cause-specific analyses revealed that MMP-8 levels were associated with mortality from both pneumonia and other forms of respiratory disease. The latter included pulmonary fibrosis, COPD, bronchitis, and bronchiectasis, but these were analysed as a single group since the numbers were too small to investigate specific sub-groups. Further research on larger cohorts of patients will be needed to determine whether MMP-8 levels are predictive of mortality from specific respiratory diseases other than pneumonia.
Apart from MMP-8 and age, the other baseline parameters most strongly associated with mortality in this study were smoking, (all-cause mortality, cancer mortality), taking CVD drugs (all cause-mortality, cardiovascular mortality), nodular disease (all-cause mortality, respiratory disease mortality), and RF (all-cause mortality, respiratory disease mortality). The findings on all-cause mortality are consistent with previous studies in RA. Although we and others have shown that higher levels of MMP-8 are associated with smoking in RA and other conditions [31, 32], our results suggest that the association of MMP-8 with all-cause and respiratory disease mortality is independent of smoking.
It is interesting that none of the other MMPs examined here were associated with mortality after adjusting for MMP-8 levels or age, sex and disease duration, even though all of the MMPs, apart from MMP-2, showed significant correlations with inflammatory and disease severity markers, and the literature on non-RA populations has reported associations of MMP-2, MMP-3 and MMP-9 levels with CVD [19–24]. In this study we found that the baseline levels of MMP-2 were significantly higher in patients who subsequently died in the follow up period, but the association disappeared after adjusting for age. This can be explained by the significant association between age and MMP-2 levels seen in the correlation analyses. Although we found no association of MMP levels with mortality from circulatory diseases in general, we did find that MMP-9 levels were associated with mortality specifically due to heart disease. This association disappeared after adjusting for patients taking CVD drugs at baseline. This can probably be explained by our data showing that these particular patients had significantly higher levels of MMP-9, and is consistent with previous studies in no-RA populations showing higher levels of MMP-9 in heart disease [19–21, 24].
The mechanisms behind the association of MMP-8 levels with mortality from respiratory disease are likely to involve the tissue destructive effects of this MMP. Several cell types may contribute towards the levels of MMP-8 but the major source is most likely to be activated neutrophils. Many previous studies have demonstrated the likely role of neutrophil-derived MMPs in the pathogenesis of respiratory diseases, including acute respiratory distress syndrome or acute lung injury [33, 34], COPD [35, 36], cystic fibrosis , interstitial lung disease , idiopathic pulmonary fibrosis  and bronchiectasis [40, 41]. Furthermore, pulmonary MMP concentrations have been shown to be elevated in patients with hospital-acquired pneumonia [42, 43]. All of these conditions are characterized by an influx of neutrophils into sites of inflammation and subsequent pulmonary tissue injury, the severity of which is associated with MMP levels [39, 40, 42, 43].
It is interesting in this study that measurement of MMP-8 levels at a single time point was predictive of long-term mortality, even though in many cases the levels were measured years before death. One possibility is that elevated MMP-8 levels may reflect chronic ongoing neutrophil activation, which may persist for many years in RA. Peripheral blood neutrophils in RA patients have been reported to be primed but show functional impairment in Fc-mediated generation of reactive oxygen species . This has been suggested to account for the increased susceptibility to bacterial infection in patients with severe RA and may explain the increase in respiratory diseases such as pneumonia. The presence of high-risk bacteria in patients with hospital-acquired pneumonia has been shown to be associated with significantly higher MMP-8 and MMP-9 levels and activity in the bronchoalveolar lavage fluid [42, 43]. It has also been reported that artificial ventilation may further promote protease activation [43, 45].
There are a number of possible limitations to the present study. Apart from determining which patients were taking CVD drugs, other comorbidities were not recorded at baseline. Various comorbid conditions may be associated with elevated levels of MMPs, so these may represent unmeasured confounders. The information on patients taking drugs for CVD problems allowed us to provide an estimate of patients suffering from cardiovascular morbidity at the time of recruitment . However, this may have been and under- or overestimate of the amount of cardiovascular morbidity present since some patients with CVD may not be taking any specific CVD drugs or may have stopped them (for example after myocardial infarction. Others may have been taking certain drugs as a preventative measure because of increased cardiovascular risk. Nonetheless our data show that patients on CVD drugs at baseline were significantly more likely to die from all-cause mortality, and heart disease in particular, than patients not on these drugs. Our data also show that patients taking CVD drugs at baseline had higher levels of MMP-2, 8 and 9 than patients not taking these drugs. However this does not explain the increased risk associated with elevated MMP-8 level, since this was associated with all-cause mortality independent of taking CVD drugs, and the latter were not associated with mortality from respiratory disease in models in which MMP-8 levels were highly significant.
A second possible limitation is the generalisability of the findings to the wider RA community since the patients studied were hospital-recruited and the study population was likely to include patients with more severe disease. The treatment of patients at baseline and during the follow up period also underwent changes in standard UK practice for treatment of hospital-based RA patients over the period 1993 to 2011. This would invariably have led to different treatment regimes based on the severity of disease at baseline, and during follow up. It is possible that different treatments may have resulted in different effects on MMP levels, but it was not possible to control for this in this study. Previous studies have indicated that the use of oral steroids is associated with increased morbidity and mortality from lower respiratory tract infections [12, 47], and we have found in a separate, previously described population of well-characterised RA patients  that those taking oral steroids have significantly higher levels of MMP-8 and MMP-9 than those not taking these drugs (unpublished observations). We have also confirmed in this second population that MMP-8 levels are associated with mortality from pneumonia, but this was independent of steroid use, which did not demonstrate a significant association (unpublished observations).
The interpretation of death certificate data is another potential limitation to the current study, especially with regard to deaths from pneumonia or chest infections when the associated or contributing cause (for example, stroke) may in fact be the main cause. However, in the current study the majority of patients dying from pneumonia (n = 23/29) had this as the only cause, or the primary cause alongside RA as an associated cause. These patients also demonstrated a highly significant association of MMP-8 levels with mortality, similar to the total group who died from pneumonia (data not shown).
Another possible limitation was the measurement of MMP levels at a single time point, and cumulative measures of MMP-8 levels during follow up may possibly have provided better predictive information. Importantly the association of MMP-8 levels with mortality was independent of traditional measures of inflammation. In the present study, single measurements of ESR and CRP at study entry were not generally predictive of mortality in models that also contained MMP-8 levels.
Our results indicate that in patients with established RA, high serum levels of MMP-8 are predictive of respiratory disease-related mortality, and provide additional predictive information on mortality in RA, which is not provided by traditional measures. These results also point to MMP-8 as a possible therapeutic target to reduce protease-mediated damage in pneumonia and other respiratory diseases in patients with RA.
chronic obstructive pulmonary disease
disease modifying anti-rheumatic drug
erythrocyte sedimentation rate
health assessment questionnaire
International Classification of Diseases
Number Cruncher Statistical System
National Health Service; National Health Service
NHS Central Register
Office for National Statistics
visual analogue score.
Symmons DP: Mortality in rheumatoid arthritis. Br J Rheumatol. 1988, 27 (Suppl I): 44-54.
Wolfe F, Mitchell DM, Sibley JT, Fries JF, Bloch DA, Williams CA, Spitz PW, Haga M, Kleinheksel SM, Cathey MA: The mortality of rheumatoid arthritis. Arthritis Rheum. 1994, 37: 481-494. 10.1002/art.1780370408.
Chehata JC, Hassell AB, Clarke SA, Mattey DL, Jones MA, Jones PW, Dawes PT: Mortality in rheumatoid arthritis: Relationship to single and composite measures of disease activity. Rheumatology. 2001, 40: 447-452. 10.1093/rheumatology/40.4.447.
Mikuls TR, Saag KG, Criswell LA, Merlino LA, Kaslow RA, Shelton BJ, Cerhan JR: Mortality risk associated with rheumatoid arthritis in a prospective cohort of older women: results from the IOWA Women's Health Study. Ann Rheum Dis. 2002, 61: 994-999. 10.1136/ard.61.11.994.
Book C, Saxne T, Jacobsson LT: Prediction of mortality in rheumatoid arthritis based on disease activity markers. J Rheumatol. 2005, 32: 430-434.
Gonzalez A, Maradit Kremers H, Crowson CS, Nicola PJ, Davis JM, Therneau TM, Roger VL, Gabriel SE: The widening mortality gap between rheumatoid arthritis patients and the general population. Arthritis Rheum. 2007, 56: 3583-3587. 10.1002/art.22979.
Wallberg Jonsson S, Ohman M-L, Johansson H, Rantapaa Dahlqvist S: Extent of inflammation predicts cardiovascular disease and overall mortality in seropositive rheumatoid arthritis. J Rheumatol. 1999, 26: 2562-2570.
Maradit-Kremers H, Nicla PJ, Crowson CS, Ballman KV, Gabriel SE: Cardiovascular death in rheumatoid arthritis: a population-based study. Arthritis Rheum. 2005, 52: 722-732. 10.1002/art.20878.
Goodson NJ, Symmons DP, Scott DGI, Bunn D, Lunt M, Silman AJ: Baseline levels of C-reactive protein and prediction of death from cardiovascular disease in patients with inflammatory polyarthritis. A ten year followup study of a primary care-based inception cohort. Arthritis Rheum. 2005, 52: 2293-2299. 10.1002/art.21204.
Solomon DH, Karlson EW, Rimm EB, Cannuscio CC, Mandl LA, Manson JE, Stampfer MJ, Curhan GC: Cardiovascular morbidity and mortality in women diagnosed with rheumatoid arthritis. Circulation. 2003, 107: 1303-1307. 10.1161/01.CIR.0000054612.26458.B2.
del Rincon I, Williams K, Stern MP, Freeman GL, Escalante A: High incidence of cardiovascular events in a rheumatoid arthritis cohort not explained by traditional cardiac risk factors. Arthritis Rheum. 2001, 44: 2737-2745. 10.1002/1529-0131(200112)44:12<2737::AID-ART460>3.0.CO;2-#.
Coyne P, Hamilton J, Heycock C, Saravanan V, Coulson E, Kelly CA: Acute lower respiratory tract infections in patients with rheumatoid arthritis. J Rheumatol. 2007, 34: 1832-1836.
Mattey DL, Glossop JR, Nixon NB, Dawes PT: Circulating levels of tumor necrosis factor receptors are highly predictive of mortality in patients with rheumatoid arthritis. Arthritis Rheum. 2007, 56: 3940-48. 10.1002/art.23075.
Cunnane G, FitzGerald O, Hummel KM, Youssef PP, Gay RE, Gay S, Bresnihan B: Synovial tissue protease gene expression and joint erosions in early rheumatoid arthritis. Arthritis Rheum. 2001, 44: 1744-1753. 10.1002/1529-0131(200108)44:8<1744::AID-ART309>3.0.CO;2-K.
Keyszer G, Lambiri I, Nagel R, Keysser C, Keysser M, Gromnica-Ihle E, Franz J, Burmester GR, Jung K: Circulating levels of matrix metalloproteinases MMP-3 and MMP-1, tissue inhibitor of metalloproteinases 1 (TIMP-1) and MMP-1/TIMP-1 complex in rheumatic disease. Correlations with clinical activity of rheumatoid arthritis versus other surrogate markers. J Rheumatol. 1999, 26: 251-258.
Cheung NT, Dawes PT, Poulton KV, Ollier WE, Taylor DJ, Mattey DL: High serum levels of pro-matrix metalloproteinase-3 are associated with greater radiographic damage and the presence of the shared epitope in patients with rheumatoid arthritis. J Rheumatol. 2000, 27: 882-887.
Yamanaka H, Matsuda Y, Tanaka M, Sendo W, Nakajima H, Taniguchi A, Kamatani N: Serum matrix metalloproteinase 3 as a predictor of the degree of joint destruction during the six months after measurement, in patients with early rheumatoid arthritis. Arthritis Rheum. 2000, 43: 852-858. 10.1002/1529-0131(200004)43:4<852::AID-ANR16>3.0.CO;2-7.
Chen Y, Nixon NB, Dawes PT, Mattey DL: Influence of variations across the MMP1 and 3 genes on the serum level of MMP-1 and -3 and disease activity in rheumatoid arthritis. Genes and Immunity. 2012, 13: 29-37. 10.1038/gene.2011.46. 14. doi: 10.1038/gene. 2011.46 Jul 14
Kalela A, Koivu TA, Sisto T, Kanervisto J, Höyhtyä M, Sillanaukee P, Lehtimäki T, Nikkari ST: Serum matrix metalloproteinase-9 concentration in angiographically assessed coronary artery disease. Scand J Clin Lab Invest. 2002, 62: 337-342. 10.1080/00365510260296483.
Blankenberg S, Rupprecht HJ, Poirier O, Bickel C, Smieja M, Hafner G, Meyer J, Cambien F, Tiret L, for the AtheroGene Investigators: Plasma concentrations and genetic variation of matrix metalloproteinase 9 and prognosis of patients with cardiovascular disease. Circulation. 2003, 107: 1579-1585. 10.1161/01.CIR.0000058700.41738.12.
Squire IB, Evans J, Ng LL, Loftus IM, Thompson MM: Plasma MMP-9 and MMP-2 following acute myocardial infarction in man: Correlation with echocardiographic and neurohumoral parameters of left ventricular dysfunction. J Card Fail. 2004, 10: 328-333. 10.1016/j.cardfail.2003.11.003.
Wu TC, Leu HB, Lin WT, Lin CP, Lin SJ, Chen JW: Plasma matrix metalloproteinase-3 level is an independent prognostic factor in stable coronary artery disease. Eur J Clin Invest. 2005, 35: 37-45.
Samnegård A, Silveira A, Lundman P, Boquist S, Odeberg J, Hulthe J, McPheat W, Tornvall P, Bergstrand L, Ericsson CG, Hamsten A, Eriksson P: Serum matrix metalloproteinase-3 concentration is influenced by MMP-3 - 1612 5A/6A promoter genotype and associated with myocardial infarction. J Intern Med. 2005, 258: 411-419. 10.1111/j.1365-2796.2005.01561.x.
Fukuda D, Shimada K, Tanaka A, Kusuyama T, Yamashita H, Ehara S, Nakamura Y, Kawarabayashi T, Iida H, Yoshiyama M, Yoshikawa J: Comparison of levels of serum matrix metalloproteinase-9 in patients with acute myocardial infarction versus unstable angina pectoris versus stable angina. Am J Cardiol. 2006, 97: 175-180. 10.1016/j.amjcard.2005.08.020.
Tuomainen AM, Nyyssonen K, Laukkanen JA, Tervahartiala T, Tuomainen T-P, Salonen JT, Sorsa T, Pussinen PJ: Serum matrix metalloproteinase-8 concentrations are associated with cardiovascular outcome in men. Arterioscler Thromb Vasc Biol. 2007, 27: 2722-2728. 10.1161/ATVBAHA.107.154831.
Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR, Liang MH, Luthra HS, Medsger TA, Mitchell DM, Neustadt DH, Pinals RS, Schaller JG, Sharp JT, Wilder RL, Hunder GG: The ARA 1987 revised criteria for classification of rheumatoid arthritis. Arthritis Rheum. 1988, 31: 315-324. 10.1002/art.1780310302.
Fries J, Spitz P, Young D: Dimensions of health outcomes: the health assessment questionnaire, disability and pain scales. J Rheumatol. 1982, 9: 789-793.
Joint Working Group of the British Society for Rheumatology and Royal College of Physicians: Guidelines and audit measures for the specialist supervision of patients with rheumatoid arthritis. J R Coll Physicians Lond. 1992, 26: 76-82.
International classification of diseases, ninth revision. 1977, Geneva: World Health Organisation
Todd DJ, Knowlton N, Amato M, Frank MB, Schur PH, Izmailova ES, Roubenoff R, Shadick NA, Weinblatt ME, Centola M, Lee DM: Erroneous augmentation of multiplex assay measurements in patients with rheumatoid arthritis due to heterophilic binding by serum rheumatoid factor. Arthritis Rheum. 2011, 63: 894-903. 10.1002/art.30213.
Aquilante CL, Beitelshees AL, Zineh I: Correlates of serum matrix metalloproteinase-8 (MMP-8) concentrations in nondiabetic subjects with cardiovascular disease. Clin Chim Acta. 2007, 379: 48-52. 10.1016/j.cca.2006.12.006.
Mattey DL, Packham JC, Nixon NB, Coates L, Creamer P, Hailwood S, Taylor GJ, Bhalla AK: Association of cytokine and matrix metalloproteinase profiles with disease activity and function in ankylosing spondylitis. Arthritis Res Ther. 2012, 14: R127-10.1186/ar3857.
Torii K, Iida K, Miyazaki Y, Saga S, Kondoh Y, Taniguchi H, Taki F, Takagi K, Matsuyama M, Suzuki R: Higher concentrations of matrix metalloproteinases in broncheolar lavage fluid of patients with adult respiratory distress syndrome. Am J Respir Crit Care Med. 1997, 155: 43-46.
Fligiel SE, Standiford T, Fligiel HM, Tashkin D, Strieter RM, Warner RL, Johnson KJ, Varani J: Matrix metalloproteianses and matrix metalloproteinase inhibitors in acute lung injury. Hum Pathol. 2006, 37: 422-430. 10.1016/j.humpath.2005.11.023.
Segura-Valdez L, Pardo A, Gaxiola M, Uhal BD, Becerril C, Selman M: Upregulation of gelatinase A and B, collagenases 1 and 2, and increased parenchymal cell death in COPD. Chest. 2000, 117: 684-694. 10.1378/chest.117.3.684.
Ilumets H, Rytilä P, Demedts I, Brusselle GG, Sovijärvi A, Myllärniemi M, Sorsa T, Kinnula VL: Matrix metalloproteianses-8, -9, and -12 in smokers and patients with stage 0 COPD. Int J Chron Obstruct Pulmon Dis. 2007, 2: 369-379.
Delacourt C, Le Boureois M, D'Ortho MP, Doit C, Scheinmann P, Navarro J, Harf A, Hartmann DJ, Lafuma C: Imbalance between 95kDa type IV collagenase and tissue inhibitor of metalloproteinases in sputum of patients with cystic fibrosis. Am J Respir Crit Care Med. 1995, 152: 765-774.
Choi KH, Lee HB, Jeong MY, Rhee YK, Chung MJ, Kwak YG, Lee YC: The role of matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in cryptogenic organizing pneumonia. Chest. 2002, 121: 1478-1485. 10.1378/chest.121.5.1478.
McKeown S, Richter AG, O'Kane C, McAuley DF, Thickett DR: MMP expression and abnormal lung permeability are important determinants of outcome in IPF. Eur Respir J. 2009, 33: 77-84. 10.1183/09031936.00060708.
Sepper R, Konttinen YT, Ding Y, Tagaki M, Sorsa T: Human neutrophil collagenase (MMP-8), identified in bronchiectasis BAL fluid, correlates with severity of disease. Chest. 1995, 107: 1641-1647. 10.1378/chest.107.6.1641.
Zheng L, Lam WK, Tipoe GL, Shum IH, Yan C, Leung R, Sun J, Ooi GC, Tsang KW: Overexpression of matrix metalloproteinase-8 and -9 in bronchiectatic airways in vivo. Eur Respir J. 2002, 20: 170-176. 10.1183/09031936.02.00282402.
Hartog CM, Wermelt JA, Sommerfeld CO, Eichler W, Dalhoff K, Braun J: Pulmonary matrix metalloproteinase excess in hospital-acquired pneumonia. Am J Respir Crit Care Med. 2003, 167: 593-598. 10.1164/rccm.200203-258OC.
Schaaf B, Liebau C, Kurowski V, Droemann D, Dalhoff K: Hospital acquired pneumonia with high-risk bacteria is associated with increased pulmonary matrix metalloproteinase activity. BMC Pulm Med. 2008, 8: 12-10.1186/1471-2466-8-12. doi:10.1186/1471-2466-8-12
Fairhurst AM, Wallace PK, Jawad AS, Goulding NJ: Rheumatoid peripheral blood phagocytes are primed for activation but have impaired Fc-mediated generation of reactive oxygen species. Arthritis Res Ther. 2007, 9: R29-10.1186/ar2144.
Albaiceta GM, Gutierrez-Fernandez A, Garcia-Prieto E, Puente XS, Parra D, Astudillo A, Campestre C, Cabrera S, Gonzalez-Lopez A, Fueyo A, Taboada F, López-Otin C: Absence or inhibition of matrix metalloproteinase-8 decreases ventilator-induced lung injury. Am J Respir Cell Mol Biol. 2010, 43: 555-563. 10.1165/rcmb.2009-0034OC.
Cannon PJ, Connell PA, Stockley IH, Garner ST, Hampton JR: Prevalence of angina as assessed by a survey of prescriptions for nitrates. Lancet. 1988, 64: 979-981.
Housden MM, Bell G, Heycock CR, Hamilton J, Saravanan V, Kelly CA: How to reduce morbidity and mortality from chest infections in rheumatoid arthritis. Clin Med. 2010, 10: 326-329.
Chen Y, Dawes PT, Packham JC, Mattey DL: Interaction between smoking and polymorphism in the promoter region of the VEGFA gene is associated with ischemic heart disease and myocardial infarction in rheumatoid arthritis. J Rheumatol. 2011, 38: 802-809. 10.3899/jrheum.101095.
We wish to thank Mrs June Fisher and Mrs Sheila Clarke (metrologists) for their help with data collection. This work was supported by the Haywood Rheumatism Research and Development Foundation.
The authors declare that they have no competing interests.
DLM and NBN carried out the biomarker measurements. DLM carried out the statistical analysis. NBN and PTD participated in the design of the study, and recruitment of patients. DLM conceived the study, participated in its design and coordination, carried out analysis and interpretation of data, and drafted the final manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Table presenting correlations between levels of matrix metalloproteinases in patients with rheumatoid arthritis at baseline. (PDF 4 KB)
Additional file 2: Table presenting correlations between clinical measures and levels of matrix metalloproteinases in patients with rheumatoid arthritis at baseline. (PDF 4 KB)
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Mattey, D.L., Nixon, N.B. & Dawes, P.T. Association of circulating levels of MMP-8 with mortality from respiratory disease in patients with rheumatoid arthritis. Arthritis Res Ther 14, R204 (2012). https://doi.org/10.1186/ar4042
- Rheumatoid Arthritis
- Chronic Obstructive Pulmonary Disease
- Rheumatoid Arthritis Patient
- Idiopathic Pulmonary Fibrosis
- Health Assessment Questionnaire