Objectives To investigate the complex relationship between inflammation, mechanical stress and radiographic progression in patients with ankylosing spondylitis (AS), using job type as a proxy for continuous mechanical stress.
Methods Patients from the Outcome in Ankylosing Spondylitis International Study were followed up for 12 years, with 2-yearly assessments. Two readers independently scored the X-rays according to the modified Stoke Ankylosing Spondylitis Spine Score (mSASSS). Disease activity was assessed by the AS Disease Activity Score C reactive protein (ASDAS-CRP). The relationship between ASDAS and spinal radiographic progression was investigated with longitudinal analysis, with job type at baseline (physically demanding (‘blue-collar’) versus sedentary (‘white-collar’) labour) as a potential factor influencing this relationship. The effects of smoking status and socioeconomic factors were also investigated.
Results In total, 184 patients were included in the analyses (70% males, 83% human leucocyte antigen-B27 positive, 39% smokers, 48% blue-collar workers (65/136 patients in whom data on job type were available)). The relationship between disease activity and radiographic progression was significantly and independently modified by job type: In ‘blue-collar’ workers versus ‘white-collar’ workers, every additional unit of ASDAS resulted in an increase of 1.2 versus 0.2 mSASSS-units/2-years (p=0.014 for the difference between blue-collar and white-collar workers). In smokers versus non-smokers, every additional unit of ASDAS resulted in an increase of 1.9 versus 0.4 mSASSS-units/2-years.
Conclusions Physically demanding jobs may amplify the potentiating effects of inflammation on bone formation in AS. Smoking and socioeconomic factors most likely confound this relationship and may have separate effects on bone formation.
- Ankylosing Spondylitis
- Disease Activity
- Outcomes research
- Received July 16, 2015.
- Revision received August 18, 2015.
- Accepted August 22, 2015.
- Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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What is already known about this subject?
Higher disease activity leads to radiographic progression in ankylosing spondylitis (AS).
What does this study add?
Physically demanding jobs may amplify the potentiating effects of inflammation on bone formation in AS.
Smoking and socioeconomic factors confound this relationship and may have separate effects on bone formation.
How might this impact on clinical practice?
More research is needed, specifically into the type of physical activity that may be deleterious and lead to radiographic progression, before these findings can have an impact on clinical practice.
In ankylosing spondylitis (AS), radiographic progression of the spine is faster in males, in human leucocyte antigen (HLA)-B27-positive patients, in patients with active disease and in those who already have signs of damage.1–5 We have recently shown that disease activity is longitudinally associated with radiographic progression.5 This effect is amplified in males and in patients with shorter symptom duration.5 Part of syndesmophyte formation was ‘constitutive’: even in the absence of disease activity patients had some progression.5 A clear and overarching biological explanation of syndesmophyte formation in AS is still lacking, but, in analogy with osteophyte formation in osteoarthritis,6 there may be a contributory role for mechanical stress.
Mice that were tail suspended, so that mechanical loading on paws was low, showed less bone formation than those kept in regular cages,7 which is a proof of concept for the proposition that mechanical strain drives new bone formation in spondyloarthritis (SpA). In addition, sparse data have suggested that jobs with physically demanding activities are associated with more radiographic damage.8
A detailed analysis of how mechanical stress and inflammation may interact in explaining radiographic progression has never been conducted, because the idea of lifetime mechanical stress is difficult to quantify and because the contribution of inflammation to syndesmophyte formation has long been obscure. However, it is rational to postulate that radiographic progression is the result of a combination of different factors (among which are disease activity and mechanical stress), rather than the sole consequence of one factor.
We have recently established the potential contribution of inflammation to radiographic progression in the Outcome in Ankylosing Spondylitis International Study (OASIS cohort), using the AS Disease Activity Score (ASDAS) as a proxy for inflammation; we have also formulated the idea of ‘constitutive progression’ (independent of inflammation).5 We think the OASIS cohort may be the appropriate template to study the interplay between inflammation and mechanical stress. In the light of the problem to quantify ‘long-term mechanical stress’, and in the absence of appropriate direct data, we have chosen ‘job type’ (physically demanding vs sedentary) as a proxy for ‘lifetime mechanical stress’ on the spine.
We have also taken potential confounders into consideration: smoking was shown to be predictive of radiographic progression in patients with axial SpA.3 It is easy to hypothesise that smoking is associated with ‘job type’, but smoking may also have an independent effect on radiographic progression. Likewise, socioeconomic factors such as personal income may interfere because they may be associated with ‘job type’.9–11
We have performed a detailed aggregated analysis focusing on the effects of ‘job type’, smoking and factors reflecting socioeconomic status on radiographic progression in AS.
Data from OASIS were used. OASIS is a prevalence cohort starting (1996) with 217 consecutive patients with AS from the Netherlands, Belgium and France.12 Clinical and radiographic (cervical and lumbar spine) data were collected every 2 years during a period of 12 years. Patients were included in the present study if they had at least two subsequent radiographs and data on disease activity as well as on occupational activities and/or smoking status and/or socioeconomic factors (educational level, personal income and/or family income) were available. All patients gave informed consent and the ethics committee from all participating hospitals approved the study.
Radiographs were scored using the modified Stoke Ankylosing Spondylitis Spine Score (mSASSS), which ranges from 0 (no damage) to 72 (maximal damage).13 Two well-trained readers (SR and CS) independently scored all available radiographs per patient, blinded to demographic and clinical data, but with known chronology.14 Mean reader scores were used. Details of the reading methodology have been reported elsewhere.1
Disease activity and occupational activity, smoking status and socioeconomic factors
Patient-reported information about occupation (collected at baseline by an open question) was used as a proxy for unmeasured lifetime mechanical stress on the spine. ‘Job type’ was determined by consensus, without knowledge of disease activity and/or radiographic damage. Two job types were distinguished: ‘blue-collar’ and ‘white-collar’ jobs, which are common circumscriptions for manual jobs (that imply more physical labour) and more sedentary jobs (that imply less physical activities), respectively.16 ,17 Examples of ‘blue-collar workers’ are craftworkers, labourers and transportation operatives. Examples of ‘white-collar workers’ are managers, administrative workers, teachers and engineers. The analyses were performed under the assumptions that (1) ‘job type’ at baseline reflects ‘lifetime job type’; and (2) ‘blue-collar jobs’ are associated with more mechanical stress on the spine than ‘white-collar jobs’.
Smokers versus non-smokers were distinguished based on baseline smoking status. If baseline information was not available, patients were retrospectively questioned in order to minimise missing data.
Socioeconomic factors were collected at baseline and included (1) educational level (collected in seven categories and dichotomised into higher professional and university education vs any other level of education; (2) baseline gross monthly personal income and family income (collected in 10 categories and dichotomised at €1588 (personal income) and €3176 (family income), respectively. These amounts demarcate income classes 1–4 versus 5–10.
The template for the analysis of the effects of ‘job type’ on radiographic progression was based on the longitudinal analysis that has been presented in detail elsewhere.5 In brief, mSASSS over time (t) (mSASSSt) was longitudinally modelled using generalised estimating equations (GEE), assuming an exchangeable working correlation structure for mSASSS in order to adjust for within-patient correlation.5
In the first model (referred to as the DIRECT model since we investigated the direct effect of ‘job type’ on radiographic progression), ‘job type’ was introduced by testing the interaction of ‘job type’ and ‘time’ on mSASSSt. Using similar methodology, we investigated the effects of smoking and the socioeconomic factors, separately and in combination with ‘job type’.
Second, the potential of the ‘job type’ to modify the established relationship between disease activity and mSASSSt5 (referred to as the INDIRECT model, as we investigated the effect of ‘job type’ on the relationship between ASDAS and radiographic progression) was analysed in our autoregressive model with 2-year time lags as proposed previously.5 Briefly, a ‘2-year time-lag’ here means that disease activity at the start of a 2-year interval (ASDASt) is associated with radiographic progression during the subsequent 2-year interval (or: mSASSSt was modelled by ASDASt−1 and by mSASSSt−1 (autoregressive component)). ‘Job type’ was tested in interaction with the longitudinal variable ‘ASDASt’. Similar INDIRECT models were run for the lifestyle factors smoking and socioeconomic factors. In the presence of relevant interactions (arbitrarily defined as interactions with p<0.1), analyses were repeated in subgroups.
Figure 1 represents graphically the DIRECT and INDIRECT models that were conducted to investigate the effects that the ‘exposure’ (eg, occupational activity) could have on radiographic damage. Note that the consequences of both models are fundamentally different.
Goodness-of-fit statistics (Quasi-likelihood under the Independence model Criterion (QIC)), with lower QICs reflecting better data fit, were used to select the best models. Owing to missing information regarding occupational activity, smoking status and the different socioeconomic factors, analyses were first conducted in all patients with each of the variables available. Next, sensitivity analysis in patients with complete data (missing family income was allowed) was conducted. None of the other measured variables in OASIS appeared to be confounders of the relationship between disease activity and radiographic progression as shown in previous analyses5 and were omitted from this analysis.
Analyses were performed using Stata SE V.12 (Statacorp, College Station, Texas, USA).
In total, 184 patients (70% males, 83% HLA-B27 positive) were included in the analyses (table 1). These patients had similar baseline characteristics as those included in the entire OASIS cohort, and patients who were followed up until year 12 were similar to those initially included in the study,5 just as those included in the sensitivity analysis (N=85; table 2). Of the 136 patients with baseline occupational activity available, 65 (48%) were assigned a ‘blue-collar’ job.
Expectedly, ‘blue-collar’ workers (86%) were more often of male gender than ‘white-collar’ workers (63%), and men (82%) were more often smokers than women (63%). Importantly, ‘blue-collar’ workers had a higher level of ASDAS than ‘white-collar’ workers, as well as a higher mSASSS at baseline (table 1). ‘White-collar’ workers had a higher level of education and a higher personal income. At baseline, none of the patients were treated with tumour necrosis factor inhibitors and 68% of the patients were treated with non-steroidal anti-inflammatory drugs. More details on this study population can be found in our previous publication.5 Information of job type over time was available for 92 patients, of whom only 1 patient had a change in job type (from blue to white collar), and even this was a temporary change; the others remained stable in their job type throughout the entire follow-up.
The DIRECT model: effects of ‘job type’ on radiographic progression
Radiographic progression was slightly but significantly higher in ‘blue-collar’ than in ‘white-collar’ workers: 2.18 mSASSS-units/2 years (95% CI 1.52 to 2.84) versus 1.82 mSASSS-units/2 years (95% CI 1.54 to 2.11) (p=0.05 for the difference between blue and white-collar workers). When investigating the effect of job type on radiographic progression in subgroups of males and females, statistical significance was lost.
Smoking (p=0.22), education (p=0.44), personal income (p=0.99) and family income (p=0.80) were not associated with radiographic progression.
The INDIRECT model: modification of the relationship between disease activity and radiographic progression by ‘job type’
The relationship between ASDAS and radiographic progression was significantly dependent on job type (p=0.014): an increase of one ASDAS-unit led to an increase of 1.2 mSASSS-units per 2 years in ‘blue-collar’ workers but only of 0.2 mSASSS units per 2 years in ‘white-collar’ workers (table 3). Similar effects were found when the analysis was performed with ‘smoking’ or ‘personal income’ instead of ‘job types’ as explanatory factors, but not with ‘educational level’ or ‘family income’. Note that the effects of ‘job type’ on this relationship (but also the effects of smoking and personal income) are seen only in men but not in women: an association between ASDAS and radiographic progression in women was almost absent.5
In a subsequent analysis, we have tried to disentangle the presumed effects of ‘job type’ and ‘smoking’ on the relationship between disease activity and radiographic progression. In the subgroup of smokers, 2-year progression per additional ASDAS-unit in ‘blue-collar’ workers (1.52 (95% CI 0.29 to 2.74) mSASSS-units) was slightly higher but not significantly different from that in ‘white-collar’ workers (1.24 (95% CI 0.09 to 2.40) mSASSS-units). In the subgroup of non-smokers, ‘blue-collar’ workers had a 2-year progression of 0.61 (95% CI 0.18 to 1.05) mSASSS progression per additional ASDAS unit increase. Unfortunately, the model did not reach convergence for ‘white-collar’ workers (35 patients). Further subgroup analyses (in gender and/or personal income strata) were impossible because of the small numbers.
When comparing the fit of the models (with each of the interaction terms included), the model with ‘smoking status’ had the best fit (QIC 4484), followed by the model with ‘job type’ (QIC 4565), personal income (QIC 5486) and finally education (QIC 5714). Note that the influence of smoking on the association between ASDAS and radiographic progression was statistically stronger than the effect of ‘job type’ on this relationship. Sensitivity analysis in patients with all variables available (except for family income due to the higher number of missing values) provided similar results (table 4).
In this study, we have proposed scientific arguments for the hypothesis that long-term physically demanding activities, here operationalised by ‘blue-collar job type’, amplify the effects of inflammation on bone (syndesmophyte) formation in AS.
We reiterate that the effect of ‘job type’ on radiographic progression was investigated in two different ways (figure 1): First, we have investigated whether ‘job type’ was associated with the course of radiographic progression itself (the DIRECT model). In fact, this turned out to be not the case: While progression was initially found to be higher in ‘blue-collar’ than in ‘white-collar’ workers, this contrast disappeared when repeating the analysis separately in males and females. We have already reported that radiographic progression was higher in men1 and ‘blue-collar’ work is primarily performed by men. The conclusion of this analysis is therefore that strenuous physical activities most likely do not have a strong DIRECT effect on radiographic progression. An intriguing alternative explanation could be that it is physical activity rather than gender that determines radiographic progression in AS, under the assumption that the intensity of physical labour is overall higher in men than in women regardless of ‘job type’. However, our study will not give further resolution.
The second type of analyses (the INDIRECT models), however, showed an effect of ‘job type’ on the reported association of ASDAS and radiographic progression:5 ‘Blue-collar’ work amplified the effect of ASDAS on radiographic progression in comparison with ‘white-collar’ work. This means that lifetime strenuous physical activities may increase the detrimental effects of inflammation on radiographic progression. If these findings are confirmed, the implications could be far stretching: the commonly given advice to patients with AS to regularly exercise in order to optimise mobility and quality of life (which is supported by a Cochrane review18 and implemented in guidelines19) may eventually need to be revised, as at least certain types of exercises or mechanical stress on the spine seem to amplify progression of structural damage. If confirmed, this would ultimately imply that (specific types of) physically demanding labour should be discouraged. In what concerns physical exercise in broader terms than professional activity, future research will need to focus on the specific types of physical activity that eventually lead to radiographic progression, to the detriment of others that are more beneficial, especially when taking all the effects of physical activity on health into account. There is some argumentation in the literature to support our findings: The amplifying effects of ‘blue-collar’ job type on the association between disease activity and radiographic progression can be a consequence of increased strenuous mechanical forces exerted on the spine. This is in concordance with what has recently been shown in animal models, in which mechanical strain has led to new bone formation.7
Unfortunately, this study does not provide sufficient explanation for several reasons. First, mechanical strain has also been shown to directly result in inflammation in animal models.7 It is plausible that physically demanding jobs in patients with AS may lead to more ‘true’ inflammation of the spine, and therefore to truly higher ASDAS levels, which in turn may explain more progression. The higher ASDAS levels we found in patients with ‘blue-collar’ jobs are concordant with such a hypothesis.
Second, we have found similar (or even stronger) interactions with other lifestyle factors such as ‘smoking’, and also with ‘socioeconomic determinants’ with regard to the association between ASDAS and radiographic progression. On the other hand, ‘job type’, ‘smoking’ and ‘socioeconomic status’ are strongly related. ‘Blue-collar’ workers, for example, are more often smokers than ‘white-collar’ workers,20 and ‘blue-collar’ workers have on average less income than ‘white-collar’ workers. The model with ‘smoking’ had a better data fit (lower QIC) than the model with ‘job type’. This raises the question of ‘what is the determinant and what is the confounder’? Is it ‘job type’ that eventually results in more progression, and is ‘smoking’ an epidemiological confounder; is it ‘smoking’ that is the primary cause of progression, and is ‘job type’ the confounder; or do both factors independently convey certain effects (figure 2)? In the appreciation that this study will not give a final verdict, biological plausibility may give some resolution: smoking has been associated in rheumatic diseases with worse outcomes, particularly in rheumatoid arthritis, where it provides an attractive explanation in the debate of citrullinisation of peptides.21 While smoking has been associated with several factors of SpA, such as early onset of back pain, more disease activity and more MRI inflammation,22–24 and it has also been associated with spinal damage in AS in one study,3 an attractive biological explanation is still lacking or at least unproven.3 Mechanical stress, on the other hand, has been brought into relation with inappropriate bone formation in several conditions such as SpA7 and osteoarthritis.6 It is therefore much more attractive and plausible to suggest that mechanical stress (here somewhat artificially operationalised as ‘blue-collar’ vs ‘white-collar’ jobs) is the causative provoking factor, and ‘smoking’—known to be associated with ‘blue-collar’ work— the confounder, rather than vice versa. An explanation that cannot be excluded is that both ‘job type’ and ‘smoking’ are independently contributory. In this discussion, we propose that ‘personal income’ and, to a lesser extent, ‘education’ and ‘family income’, while being proven modifiers of the relationship between ASDAS and radiographic progression, do not have biological plausibility and should be considered as confounders, id est: ‘personal income’ and others are subordinate to ‘job type’. In analogy with many rheumatic diseases, the association of socioeconomic variables with outcome of disease also is intriguingly present here.25–28
As far as we know, the role of occupational activities, smoking or socioeconomic factors on the course of radiographic progression over the long term has not been investigated previously and we cannot compare our findings with others.
This study has several additional limitations worth mentioning. The sample size of this observational study is not large enough to allow subtle but complex relationships in critically relevant subgroups (eg, smokers vs non-smokers and men vs women). On the other hand, larger cohorts without biological treatment but a more meticulous follow-up than this one will most likely never be conducted.
An important limitation is that we assumed the dichotomy of ‘blue-collar’ versus ‘white-collar’ jobs as being representative of a high versus low level of mechanical stress on the spine. We cannot exclude the possibility that ‘white-collar’ workers follow more thoroughly the physicians’ recommendations to intensively exercise and thus compensate lower levels of physical activity during working hours with higher levels of exercise. However, regardless of what epidemiological mechanism may have worked against the effects of ‘job type’, the effects are significant and relevant.
Another limitation of this study is that we have modelled ‘job type’ at baseline as being representative of ‘job type’ during follow-up. However, from the patients with data on job type over time available, only one patient changed his job type, which confirms that people tend to practise the same type of profession over several years. Moreover, since OASIS is not an inception cohort but symptom duration was on average 20 years at the start, it is most likely that changes due to the onset of back pain are made before the inclusion in the cohort.
What impact do the findings in this study and the previous one5 have with regard to explaining syndesmophyte formation in AS? We have previously identified important determinants of syndesmophyte formation in patients with AS: it occurs primarily in HLA-B27-positive male patients, reiterating the constitutive (genetic) component.1 Disease activity (inflammation) does have an influence on the rate of progression, but primarily in (genetically) susceptible (male) patients.5 In addition, we have now made likely that—among other factors still to be identified—lifetime physical activities during working hours may amplify the detrimental effects of inflammation on radiographic progression. Whether smoking is an independent modifier of this relationship or only a confounder still needs to be elucidated.
- Received July 16, 2015.
- Revision received August 18, 2015.
- Accepted August 22, 2015.
Contributors SR, RL, AvT, AB and DvdH designed the study. SR, RL, AvT, AB, CS, FvdB, MD and DvdH collected the data. SR and CS read the radiographs. AvT was the adjudicator. SR, RL, AvT, AB and DvdH analysed the data and critically interpreted the results. SR prepared the first version of the manuscript. All authors reviewed the draft versions and gave their approval of the final version of the manuscript.
Funding SR was supported by the Fundação para a Ciência e Tecnologia (FCT) grant SFRH/BD/68684/2010
Competing interests None declared.
Patient consent Obtained.
Ethics approval The ethics committee from all participating hospitals approved the study (Paris, Maastricht, Ghent).
Provenance and peer review Not commissioned; externally peer reviewed.
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