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Ankylosing spondylitis: recent breakthroughs in diagnosis and treatment.


Ankylosing spondylitis (AS) is the prototype disease within the spondyloarthropathies (SpA), a group of diseases presenting mainly with inflammation of the axial skeleton, peripheral arthritis and enthesitis (inflammation at insertion sites of bone to tendons, ligaments, and joint capsules). This disorder is in fact a systemic disease, causing numerous extraskeletal manifestations that have a significant influence on patient prognosis. Included among these accompanying features are inflammatory bowel disease, acute anterior uveitis (iritis), and psoriasis. In addition, there is a strong association with the HLA-B27 antigen and a familial aggregation.

It is estimated that AS affects about 0.5% of the population and male to female ratio is roughly 2:1. (1-3) In comparison, rheumatoid arthritis is seen in about 1% of most populations. (4) Ankylosing spondylitis most commonly has its onset while a patient is in their twenties, although late teenage years are also relatively common for initial symptoms. (5) The disease onset is at a younger age and acute iritis is more common in B27 positive as compared to B27 negative patients. (6) In a study of 1080 patients (90% HLA-B27 positive), the average age of onset in B27 positive patients was 24.8 years, whereas in those that were B27 negative it was 27.7 years. (5) It is very unusual to have a patient present with this disorder beyond forty-five years old. A common diagnosis that is mistaken for AS in the more advanced aged groups would be diffuse idiopathic skeletal hyperostosis (DISH). In this condition, the sacroiliac joints are typically spared and there is usually a more flowing and bulky ossification of the anterior longitudinal ligament, rather than the syndesmophytes of AS that bridge between the vertebral body corners and include the annular fibers of the intervertebral discs.

The objectives of this paper will be to provide rationale for more early and accurate diagnosis of AS, despite the difficulties associated with radiographs and the lack of a single pathognomonic clinical feature or laboratory test. In addition, updates in management, including the newer anti-tumor necrosis factor (TNF) agents, will be discussed.


Inflammatory back pain

The main symptom of AS is inflammatory back pain (IBP). There are several features that can help differentiate IBP from mechanical low back pain (MLBP). The value of the clinical history in differentiating IBP from MLBP has been investigated and refined by Rudwaleit and colleagues, by comparing the clinical history of 213 patients (101 with AS and 112 with MLBP) younger than 50 years who had chronic back pain. (7) The features that are most helpful in differentiating IBP from MLBP are outlined in Figure 1.

This analysis yielded a sensitivity of 70.3% and a specificity of 81.2% if 2 of these 4 parameters were fulfilled (positive likelihood ratio 3.7). If 3 of the 4 parameters were fulfilled, the positive likelihood ratio increased to 12.4.7 Importantly, none of the single parameters alone sufficiently differentiated AS from MLBP. In contrast, several sets of combined parameters proved to be well balanced between sensitivity and specificity.
Figure 1 Features in the clinical history differentiating inflammatory
back pain from mechanical low back pain.

1. morning stiffness of >30 minutes' duration

2. improvement in back pain with exercise but not with rest

3. awakening because of back pain during the second half of the night

4. alternating buttock pain

Apart from affecting the complete axial skeleton, AS can also involve peripheral joints. Often the ribcage joints such as the costovertebral and costotransverse articulations and less often the manubriosternal and costochondral junctions may be involved, and this can result in pain with coughing or sneezing as well as local tenderness. The more common joints affected include the hips and shoulders. Patients with concomitant psoriasis tend to get more peripheral joint involvement.


The concept of enthesitis has emerged as an important contributor to the inflammatory process involved in AS. Inflammatory cell infiltrates invading the adjacent bone at the enthesis (bony sites of ligamentous attachments) have been well described. (8) Bone marrow changes have also been observed in the vertebrae of some AS patient. (9) Magnetic resonance imaging (MRI) using fat suppression techniques has confirmed that the extracapsular changes taking place in inflamed synovial joints of patients with AS commonly involve the entheses. (10) In the spine, enthesitis occurs at capsular and ligamentous attachments at discovertebral, costovertebral, costotransverse, and facet joints. Involvement can also be present at the bony attachments of interspinous and supraspinous ligaments. Some of the more common peripheral entheseal sites that can be affected are located around the shoulders, hips, and the plantar fascia and Achilles insertions on the calcaneus.

Extraarticular manifestations

Acute anterior uveitis (also referred to as iritis) is a well recognized feature associated with AS and one or more attacks are seen in 20-40% of AS patients. (11-12) The typi cal presentation is a sudden onset of eye pain, redness, visual blurriness, and photophobia. Some cases can be chronic and lead to permanent visual impairment. Psoriasis is seen in about 9% and inflammatory bowel disease (Crohn's disease and ulcerative colitis) in up to 6% of those with AS. (13-14) Both of these co-morbidities seem to be associated with more severe AS disease activity and poorer functioning. (15) There are also several associated cardiovascular features, such as aortic insufficiency, conduction abnormalities, and an increased risk of myocardial infarction. (16-18) Patients with AS are at an increased risk of sustaining vertebral compression fractures because of a heightened incidence of osteoporosis, spinal rigidity, and kyphosis. A population-based study in Minnesota found that the prevalence of thoracolumbar compression fractures in AS sufferers was 7.6 times higher compared with the population rates. (19) Another study revealed that 47% of the vertebral compression fractures in AS patients resulted in some form of neurological complication ranging from transient paresthesia to loss of strength in a limb. (20)

Disease burden

In addition to the obvious deleterious effects on quality of life, there is also a substantial economic burden associated with AS. When looked at in a large Canadian study, the mean annual overall costs associated with the disease was CDN$9,008, with indirect cost accounting for 38% of the total. Total costs increased with diminishing physical function as measured by the Bath Ankylosing Spondylitis Functional Index (BASFI). For example, a BASFI >7 resulted in mean annual costs of CDN$23,300. (21) Longer disease duration, increased age, and smoking have been shown to be associated with decreased functioning. (22) The indirect costs related to AS are mostly from disability payments due to withdrawal from the workforce in addition to early retirement. (23) Contrary to previous beliefs, the condition doesn't 'burn out' over time, but instead typically continues to be active for decades. (24) However, the majority of loss of function occurs in the first ten years from disease onset. (24) The burden of this disease in terms of reduced quality of life, risk of unemployment, and overall direct and indirect healthcare costs are similar to rheumatoid arthritis. (25) However, since AS usually starts in early adulthood, there is a longer overall disease duration when compared to aged-matched patients with rheumatoid arthritis. Therefore, AS patients have to adjust to their disease for most of their lives.

Making the diagnosis earlier where chiropractors can make a difference

Back pain is the predominant reason for a referral to a chiropractor. The prevalence of sacroiliac joint disease in lumbar spine and AP pelvis x-rays taken at the Canadian Memorial Chiropractic College has been studied. (26) Findings showed that 23.2% of the cohort had degenerative changes in the sacroiliac joints compared to 3.8% having definite criteria for sacroiliitis consistent with AS. Another 4.1% had possible inflammatory changes (<Grade II bilateral sacroiliitis). The inflammatory changes were more prevalent in male patients and those with a younger mean age. (26)

Making a diagnosis of AS can be challenging. (27) It is quite common for the diagnosis of AS to be missed or markedly delayed, (28) particularly in the primary care setting.(29) On average, there is a 7-10 year delay in the diagnosis of this disease from the onset of symptoms. (5) There are a number of factors that contribute to the delay in diagnosis. First, the majority of back pain sufferers do not seek care from healthcare providers. Young men tend to be the segment of the population that are the least likely to do so. When care is sought, the most common source is a general practitioner or chiropractor. (30) Since AS has a predilection to affect young males, these findings would suggest that a substantial amount of sufferers do not even get assessed. Second, the existing criteria, namely the modified New York Criteria, requires advanced radiographic changes to be present in the sacroiliac joints. (31) Unequivocal sacroiliitis of at least grade 2 bilaterally or grade 3 unilaterally plus clinical symptoms is required before a diagnosis of ankylosing spondylitis can be made. These changes usually lag several years after the onset of axial pain and stiff ness, despite the presence of inflammation as detected by MRI. Thus, the established classification criteria for AS is more suited for picking up advanced disease.

In order for chiropractors or other practitioners to make a more accurate diagnosis of axial SpA in its early stages (pre-radiographic AS), there are certain clinical features that have been proven to increase the disease likelihood. These features have been assigned probabilities and a diagnostic algorithm has been devised by Rudwaleit, et al. (28) As a starting point, a 5% prevalence of axial SpA among patients with chronic LBP presenting to their primary care provider was used. Apart from radiographic sacroiliitis, some of the clinical features that increased the likelihood of axial SpA were: positive MRI (likelihood ratio [LR] of 9.0), positive HLA-B27 (LR = 9.0), history of acute iritis (uveitis) (LR = 7.3), positive family history (LR = 6.4), and a positive response to NSAIDs (LR = 5.1). (28) In the assessment it would be important for the chiropractor to assess for characteristics of inflammatory back pain (see Figure 1) and clinical features such as uveitis, positive family history of SpA, response to NSAIDs, peripheral joint swelling, or presence of inflammatory bowel disease or psoriasis.

The role of MRI in diagnosis

Recent use of MRI has confirmed that active inflammation is present in the spine and/or sacroiliac joints long before the appearance of unequivocal changes of sacroiliitis on plain radiographs. (32) Therefore the absence of radiologic sacroiliitis should not rule out the diagnosis of AS. Magnetic resonance imaging is now clearly established as a sensitive and specific tool to detect sacroiliitis. (33-34) MRI findings include a decrease in signal intensity in the subchondral marrow on T1-weighted images, whereas an increase in signal intensity is seen on T2-weighted images. These changes represent inflammation of edematous tissue. Blum and colleagues demonstrated that when used to detect active sacroiliitis, MRI was 95% (20 out of 21) sensitive and 100% (43 out of 43) specific, whereas plain radiography was only 19% (4 out of 21) sensitive and 47% (20 out of 43) specific. (33) MRI has also helped define the role of enthesitis in the evolution of the pathology in the early stages of SpAs. (35) Fat-suppressed MRI techniques have detected an inflammatory response involving the soft tissues and underlying bone marrow in an extensive area around the enthesis. MRI has also provided in formation to suggest the observed synovial and cartilage changes in SpAs are mainly due to an entheseal rather than synovial-based pathology. (35) The main use for MRI in the management of AS is in establishing early diagnosis and with distinguishing active inflammatory axial disease from non-inflammatory causes. An example would be the patient with inflammatory back pain who does not have definite radiologic sacroiliitis. An MRI can show inflammation, bone marrow edema, and pre-radiographic erosions at the sacroiliac joints. The short-tau inversion recovery (STIR) technique is able to show these changes well without having to use the addition of the added cost of gadolinium enhancement. (36) Computerized tomography is more accurate than plain radiography for morpho logical changes in the sacroiliac joints but cannot differentiate active from inactive disease. (37-38)



Until recently treatment options for AS have been limited. Physical therapy techniques and non-steroidal anti-inflammatory drugs (NSAIDs) have been the mainstay of therapy in these patients. No real disease modifying antirheumatic treatment was previously available. There are multiple therapies such as methotrexate, sulfasalazine, and leflunomide that have proven efficacious in rheumatoid arthritis. However, all of these have failed to provide substantial benefit from the often disabling axial symptoms and signs of AS. (39-41) Therefore, a previous delayed diagnosis did not have the same perceived adverse consequences because of the lack of highly effective therapeutic choices.

Some patients with milder forms of the disease can achieve success with exercise and physical therapy. (42-45) There is consistent evidence in the form of randomized, placebo controlled trials to show that NSAIDs and cyclooxygenase-2 specific inhibitors (coxibs) are superior to placebo in improving spinal pain. (46-51) In addition, NSAIDs may have a protective effect on structural damage when taken on a regular basis. (52) Safety concerns, particularly with gastrointestinal (GI) bleeding and cardiovascular toxicity limit the use of these agents in many patients. (53-55) These side effects appear to be dosedependent. (56) Despite traditional management approaches (education, exercise, physical therapy, and NSAIDs) remaining important, there are a sizeable proportion of patients that will continue to do poorly. In a German study conducted in 2000, there were 1080 AS patients who replied through questionnaires. Seventy-eight percent had regularly taken NSAIDs for their disease 12 months prior to the study. 19.1% reported complete pain control, 26.8% reported pain reduction to one quarter, and a further 34.4% reported pain reduction to one half. However, over 20% of patients taking NSAIDs still reported insufficient pain control and more than 40% changed the NSAID due to lack of efficacy. One quarter of AS patients reported severe side effects from their treatment, most commonly abdominal pain, headache, dizziness, and nausea. The percentage of AS patients reporting changing their NSAID due to side effects ranged from 10.5% for celecoxib to 31.4% for indomethacin. (57) Another study, from the United Kingdom, involving 246 participants with AS, revealed that 64% of the respondants had a Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) score greater than 4 out of 10. The group of patients with BASDAI scores above 4 correlated with greater pain scores (assessed with a 0-10 cm VAS composite score), higher BASFI scores (worse functioning) and poorer quality of life scores compared to those AS patients with a BASDAI below 4. (58) These studies underscore the need for more effective treatments. Apart from being ineffective or poorly tolerated many of the above modalities offer little help in arresting or delaying the progression of the disease. (59) Consequences of poor disease control may include diminished quality of life, which extends into the context of work disability and early retirement.

New treatment approaches

Since 2000 considerable progress has taken place in the therapeutic approach to SpA. This progress is due in large part to the development of effective biologic therapies and to improved clinical trial design and implementation. TNF-alpha blocking agents (monoclonal antibodies or soluble receptors) are the first representative drugs, of which the indication has recently been expanded to also encompass patients with AS. TNF-alpha is a pro-inflammatory cytokine that is involved in the pathogenesis of AS and related SpA, in addition to psoriasis, and inflammatory bowel disease. (60) It appears to be key in the inflammatory response observed in AS. The detection of an abundance of TNF messenger RNA has been documented in synovial biopsies from sacroiliac joints in patients with AS (Figure 3). (61)

Most recently, it has been convincingly demonstrated that the TNF-alpha blocking agents infliximab, etanercept, and adalimumab have a strong and prompt effect on almost all features of AS. All three of these medications have demonstrated their benefits in large-scale randomized, double-blind, placebo-controlled trials. (62-64) These agents now make it possible to suppress disease activity, improve physical function, and slow disease progression. It is worthwhile noting that the AS patients that have been studied in these large-scale studies were those whose disease was refractory to NSAIDs and physical therapy. In addition, the studied patients in these trials were required to have active disease, demonstrated by a BASDAI (Bath Ankylosing Spondylitis Disease Activity Index) greater than 4.
   Infliximab is given as an intravenous infusion every six to eight
   weeks. In addition to the benefits on the axial and peripheral
   joint symptoms, there are also beneficial effects on those with
   concomitant inflammatory bowel disease (IBD), uveitis, and
   psoriasis. (65-67)

   Etanercept is given as a subcutaneous injection, weekly or
   biweekly. It also is highly effective for the signs and symptoms of
   AS. There is the added benefit of it being effective in psoriasis,
   however it is less useful for the symptoms of IBD and uveitis.

   Adalimumab is dosed every other week in the form of a subcutaneous
   injection. Like Infliximab, it is effective in psoriasis and IBD.
   (68) At the moment, insufficient information is available regarding


There is now long term evidence to support anti-TNF treatment. Infliximab has demonstrated efficacy and safety for up to five years in an open-label study of patients with moderate to severe AS. (69) In this study, a durable sustained response was observed, with the mean BASDAI score prior to treatment being 6.4 and after five years it was 2.5. Impressively, 34% of the patients were in clinical remission. In the placebo-controlled studies, there is two year evidence for infliximab and etanercept and one year for adalimumab. (70-72)

In addition, to spinal pain and stiffness, there is also notable improvement with peripheral arthritis and enthesitis. Clinical indicators of disease activity, such as juxta-articular bony inflammation that can be seen by MRI, can be suppressed quite dramatically by TNF-alpha blockers. (73-75) (see Figure 4) Less radiographic progression after 2 and 4 years of continuous treatment with infliximab compared to conventional therapy has been suggested in a small continuous study. (76,77) The erythro cyte sedimentation rate (ESR) and C-reactive protein (CRP) are acute phase reactants in blood serum that may be raised in patients with AS when the disease is more active. Both the ESR and CRP also tend to be lowered with this class of medications. (61-63)

There is some data that suggests that AS patients with a short disease duration and younger age are more likely to respond to TNF-alpha blocking agents. (78) Thus, underscoring that an early and reliable diagnosis of AS has now become an important and very relevant issue. In all of the larger studies, major side effects were low and minor side effects were mostly in the form of mild infections, although opportunistic infection such as the reactivation of tuberculosis can be more common. (79) Infasion and injection site reactions can also occur but are generally quite manageable. Patients with a history of a solid organ malignancy or melanoma may not be appropriate candidates for TNF blockers because of a lack of information on experience with these subgroups.

Patient access to the anti-TNF therapies is somewhat restrictive, mostly because of the associated high costs of the medications. It is common practice to file applications with private health insurance plans or with provin cial health ministries in Canada to obtain anti-TNF agents. This process usually requires the cooperation and know-how of a rheumatologist.



Now that there are medications that are highly effective in treating AS, it is more of a priority to diagnose this condition earlier. There are now proposed clinical path ways to make an earlier diagnosis prior to established radiographic changes becoming present. (28) It is important to differentiate inflammatory from mechanical back pain symptoms. Moreover, consideration should be given to some of the extraskeletal manifestations, such as uveitis, inflammatory bowel disease, and psoriasis that when present can be helpful in determining the likelihood of a person having AS. MRI of the sacroiliac joints and spine also has a role in diagnosis in earlier stages of the disease when inflammation can be detected at a time when radiographs usually appear normal or equivocal.

The AS patient that fails conservative measures and NSAIDs, is the one that needs to be identified and considered for anti-TNF therapies as second-line treatments. The evidence shows that, unlike RA, the so-called "disease modifying" drugs like methotrexate, sulfasalazine, and leflunomide have proven to be ineffective in AS. The TNF blocking agents currently available, infliximab (Remicade), etanercept (Enbrel), and adalimumab (Humira), are approved for the treatment of AS in Canada. We are now in an era where not only symptoms can be targeted, but slowing down and possibly achieving clinical remission of a disease is possible. The implementation and follow up care should be undertaken by an experienced healthcare provider such as a rheumatologist specialized in their use, because of the specifics involved with drug access, tools to measure response to therapy, and the monitoring of potential side effects.

Chiropractors have a significant role to play in Canada's health care system in addressing the burdens of disease related to back pain, particularly with respect to AS. This includes the primary care setting where chiropractors, in making an earlier diagnosis differentiating inflammatory back pain from mechanical back pain are able to facilitate the AS patient's best interest.

For review of this manuscript, special acknowledgement is made to Muhammad Asim Khan, MD, FACP, FRCP, Professor of Medicine, Case Western Reserve University School of Medicine, MetroHealth Medical Center, Cleveland, Ohio 44109, USA.


(1) van der Linden S, Valkenburg HA, de Jongh BM, Cats A. The risk of developing ankylosing spondylitis in HLA-B27 positive individuals: a comparison of relatives of spondylitis patients with the general population. Arthritis Rheum 1984; 27:241-9.

(2) Gran JT, Husby G, Hordvik M. Prevalence of ankylosing spondylitis in males and females in a young middle-aged population in Troms0, northern Norway. Ann Rheum Dis 1985; 44:359-67.

(3) Braun J, Bollow M, Remlinger G, Eggens U, Rudwaleit M, Distler A, et al. Prevalence of spondylarthropathies in HLA-B27 positive and negative blood donors. Arthritis Rheum 1998; 41:58-67.

(4) Sieper J, Rudwaleit M, Khan MA, Braun J. Concepts and epidemiology of spondyloarthritis. Best Pract Res Clin Rheumatol 2006; Jun;20(3):401-17.

(5) Feldtkeller E, Khan MA, van der Heijde D, van der Linden S, Braun J. Age at disease onset and diagnosis delay in HLA-B27negative vs. positive patients with ankylosing spondylitis. Rheumatol Int 2003; 23:61-6.

(6) Khan MA, Kushner I, Braun WE. Comparison of clinical features of HLA-B27 positive and negative patients with ankylosing spondylitis. Arthritis Rheum 1977; 20:909-12.

(7) Rudwaleit M, Metter A, Listing J, Sieper J, Braun J. Inflammatory back pain in ankylosing spondylitis: a reassessment of the clinical history for application as classification and diagnostic criteria. Arthritis Rheum. 2006 Feb; 54(2):569-78.

(8) Ball J. Enthesopathy in rheumatoid ankylosing spondylitis. Ann Rheum Dis 1971; 30:213-23.

(9) Cawley MID, Chalmers TM, Kellgren JH, et al. Destructive lesions of the vertebral bodies in ankylosing spondylitis. Ann Rheum Dis 1972; 31:345-58.

(10) McGonagle D, Khan MA, Marzo-Ortega H, et al. Enthesitis in spondyloarthropathy. Curr Opin Rheumatol 1999; 11:244-50.

(11) Khan MA. Spondyloarthropathies. In: Hunder GG, editor. Atlas of rheumatology. Philadelphia: Current Medicine, 2002: 141-67.

(12) Banares A, Hernandez-Garcia C, Fernandez-Gutierrez B, Jover JA. Eye involvement in the spondyloarthropathies. Rheum Dis Clin North Am 1998; 24:771-84, ix.

(13) Edmunds L, Elswood J, Kennedy LG, Calin A. Primary ankylosing spondylitis, psoriatic and enteropathic spondyloarthropathy: a controlled analysis. J Rheumatol 1991; 18:696-8.

(14) Baetan D, De Keyser F, Mielants H, Veys EM. Ankylosing spondylitis and bowel disease. Best Pract Res Clin Rheumatol 2002; 16:537-49.

(15) Brophy S, Pavy S, Lewis P, et al. Inflammatory eye, skin, and bowel disease in spondyloarthritis: genetic, phenotypic, and environmental factors. J Rheumatol 2001; 28:2667-73.

(16) Khan MA, Khan MK, Kushner I. Survival among patients with ankylosing spondylitis: a life- table analysis. J Rheumatol 1981; 8:86-90.

(17) Sun JP, Khan MA, Farhat AZ, Bahler RC. Alterations in cardiac diastolic function in patients with ankylosing spondylitis. Int J Cardiol 1992; 37:65-72.

(18) Peters MJ, van der Horst-Bruinsma IE, Dijkmans BA, Nurmohamed MT. Cardiovascular risk profile of patients with spodyloarthropathies, particularly ankylosing spondylitis and psoriatic arthritis. Semin Arthritis Rheum 2004; 34:585-92.

(19) Cooper C, Carbone L, Michet CJ, Atkinson EJ, O'Fallon WM, Melton LJ 3rd. Fracture risk in patients with ankylosing spondylitis: a population based study. J Rheumatol 1994; 21:1877-82.

(20) Vosse D, Feldtkeller E, Erlendsson J, Gausens P, van der Linden S. Prevalence and annual incidence of vertebral fractures in patients with ankylosing spondylitis. J Rheumatol 2004; 31:1981-5.

(21) Kobelt G, Andlin-Sobocki P, Maksymowych WP. Costs and quality of life of patients with ankylosing spondylitis in Canada. J Rheumatol 2006 Feb; 33(2):289-95.

(22) Ward MM. Predictors of the progression of functional disability in patients with ankylosing spondylitis. J Rheumatol 2002; 29:1420-5.

(23) Boonen A, Chorus A, Miedema H, van der Heijde D, van der tempel H, van der Linden S. Employment work disability, and work days lost in patients with ankylosing spondylitis: a cross sectional study of Dutch patients. Ann Rheum Dis 2001; 60:353-8.

(24) Gran JT, Skomsvoll JF. The outcome of ankylosing spondylitis: A study of 100 patients. Br J Rheumatol 1997; 36:766-771.

(25) Braun J, Pincus T. Mortality, course of disease and prognosis of patients with ankylosing spondylitis. Clin Exp Rheumatol 2002;Nov-Dec; 20(6 Suppl 28):S16-22.

(26) O'Shea FD, Salonen D, Ammendolia C, Hsu W, Peterson C, Inman RD. Front line back pain: The prevalence of sacroiliac joint disease in a primary back pain cohort. Arthritis Rheum 2006; 54(9): suppl.

(27) Elyan M, Khan MA. Diagnosing ankylosing spondylitis. J Rheumatol 2006; 33 Suppl 78:12-23.

(28) Rudwaleit M, Khan MA, Sieper J. The challenge of diagnosis and classification in early ankylosing spondylitis: do we need new criteria? Arthritis Rheum 2005 Apr; 52(4):1000-8.

(29) Boyer GS, Templin DW, Bowler A, et al. A comparison of patients with spondyloarthropathy seen in specialty clinics with those identified in a communitywide epidemiological study. Has the classic case misled us? Arch Intern Med 1997; 157:2111-7.

(30) Walker BF, Muller R, Grant WD. Low back pain in Australian adults, health provider utilization and care seeking. J Manipulative Physiol Ther 2004 Jun; 27(5):327-35.

(31) van der Linden S, Valkenburg HA, Cats A. Evaluation of diagnostic criteria for ankylosing spondylitis. Arthritis Rheum 1984; 27:361-368.

(32) Oostveen J, Prevo R, den Boer J, van de Laar M. Early detection of sacroiliitis on magnetic resonance imaging and subsequent development of sacroiliitis on plain radiography. A prospective, longitudinal study. J Rheumatol 1999; 26:1953-8.

(33) Blum U, Buitrago-Tellez C, Mundinger A, et al. Magnetic resonance imaging (MRI) for detection of active sacroiliitis -- a prospective study comparing conventional radiography, scintigraphy, and contrast enhanced MRI. J Rheumatol 1996; 23:2107-2115.

(34) Khan MA. Spondyloarthropathies - editorial review. Curr Opin Rheumatol 1999; 11:233-234.

(35) McGonagle D, Gibbon W, O'Connor P, et al. Characteristic MRI entheseal changes of knee synovitis in spondyloarthropathy. Arthritis Rheum 1998; 41:694-700.

(36) Baraliakos X, Hermann KG, Landewe R, et al. Assessment of acute spinal inflammation in patients with ankylosing spondylitis by magnetic resonance imaging: a comparison between contrast enhanced T1 and short tau inversion recovery (STIR) sequences. Ann Rheum Dis 2005; 64:1141-4.

(37) Borlaza GS, Siegel R, Kuhns LR, et al. Computed tomography in the evaluation of sacroiliitis. Am J Rheumatol 1982; 139:577-581.

(38) Battafarano DF, West SD, Rak KM, et al. Comparison of bone scan, computed tomography and magnetic resonance imaging in the diagnosis of acute sacroiliitis. Semin Arthritis Rheum 1993; 23:161-176.

(39) Chen J, Liu C. Methotrexate for ankylosing spondylitis. Cochrane Database Syst Rev 2004;3:CD004524.

(40) Braun J, Alten R, Burmester G, Ebner W, Gomor B, Grasedyck K, et al. Efficacy of sulfasalazine in undifferentiated spondyloarthritis and early ankylosing spondylitis: a multicenter randomized controlled trial. Ann Rheum Dis 2006 Sep; 65(9):1147-53.

(41) Van Denderen JC, van der Paardt M, Nurmohamed MT, de Ryck YM, Dijkmans BA, van der Horst-Bruinsma IE. Double-blind, randomised, placebo-controlled study of leflunomide in the treatment of active ankylosing spondylitis. Ann Rheum Dis 2005 Dec; 64(12):1761-4.

(42) Kraag G, Stokes B, Groh J, Helewa A, Goldsmith CH. The effects of comprehensive home physiotherapy and supervision on patients with ankylosing spondylitis-an 8 month follow up. J Rheumatol 1994; 21:261-3.

(43) Hidding A, van der Linden S, Boers M, Gielen X, de Witte L, Kester A, et al. Is group pysical therapy superior to individualized therapy in ankylosing spondylitis? A randomized controlled trial. Arthritis Care Res 1993; 6:117-125.

(44) Helliwel PS, Abbott CA, Chamberlain MA. A randomized trial of three different physiotherapy regimes in ankylosing spondylitis. Physiotherapy 1996; 82:85-90.

(45) Sweeney S, Taylor G, Calin A. The effect of a home based exercise intervention package on outcome in ankylosing spondylitis: a randomized controlled trial. J Rheumatol 2002; 29:763-766.

(46) Dougados M, Nguyen M, Caporal R, Legeais J, BouxinSauzet A, Pellegri-Geugnault B, et al. Ximoprofen in ankylosing spondylitis. A double blind placebo controlled dose ranging study. Scand J Rheumatol 1994; 23:243-248.

(47) Dougados M, Caporal R, Doury P, Thiesce A, Pattin S, Laffez B, et al. A double blind crossover trial of ximoprofen in ankylosing spondylitis. J Rheumatol 1989; 16:1167-1169.

(48) Sturrock RD, Hart FD. Double-blind cross-over comparison of indomethacin, flubiprofen, and placebo in ankylosing spondylitis. Ann Rheum Dis 1974; 33:129-131.

(49) Dougados M, Gueguen A, Nakache JP, Velicitat P, Veys EM, Zeidler H, et al. Ankylosing Spondylitis: what is the optimum duration of a clinical study? A one year versus a 6 weeks non-steroidal anti-inflammatory drug trial. Rheumatology (Oxford) 1999; 38:235-244.

(50) Dougados M, Behier JM, Jolchine I, Calin A, van der Heijde D, Olivieri I, et al. Efficacy of celecoxib, a cyclooxygenase-2 specific inhibitor, in the treatment of ankylosing spondylitis: a 6 week controlled study with comparison against placebo and against conventional nonsteroidal anti-inflammatory drug. Arthritis Rheum 2001; 44:180-185.

(51) van der Heijde D, Baraf HSB, Ramos-Remus C, Calin A, Weaver AL, Schiff M, et al. Evaluation of the efficacy of etoricoxib in ankylosing spondylitis: results of a 52-week randomized controlled study. Arthritis Rheum 2005; 52:1205-1215.

(52) Wanders A, van der Heijde D, Landewe R, et al. Nonsteroidal anti-inflammatory drugs reduce radiographic progression in patients with ankylosing spondylitis: a randomized clinical trial. Arthritis Rheum 2005; 52:1756-65.

(53) Gabriel SE, Jaakkimainen L, Bombardier C. Risk for serious gastrointestinal complications related to use of nonsteroidal antiinflammatory drugs. A meta-analysis. Ann Intern Med 1991; 115:787-796.

(54) Ofman JJ, MacLean CH, Straus WL, Morton SC, Berger ML, Roth EA, et al. A metanalysis of severe upper gastrointestinal complications of nonsteroidal antiinflammatory drugs. J Rheumatol 2002; 29:804-812.

(55) McGettigan P, Henry D. Cardiovascular Risk and Inhibition of Cyclooxygenase: A Systematic Review of the Observational Studies of Selective and Nonselective Inhibitors of Cyclooxygenase 2. JAMA 2006 Oct 4; 296(13):1633-44.

(56) Lewis SC, Langman MJ, Laporte JR, Matthews JN, Rawlins MD, Wilholm BE. Dose-response relationships between individual nonaspirin nonsteroidal antiinflammatory drugs (NANSAIDs) and serious upper gastrointestinal bleeding: a meta-analysis based on individual patient data. Br J Clin Pharmacol 2002; 54:320326.

(57) Zochling J, Bohl-Buhler MH, Baraliakos X, Feldtkeller E, Braun J. Nonsteroidal anti-inflammatory drug use in ankylosing spondylitis-a population-based survey. Clin Rheumatol 2006 Nov; 25(6):794-800.

(58) Barkham N, Kong KO, Tennant A, Fraser A, Hensor E, Keenan AM, Emery P. The unmet need for anti-tumour necrosis factor (anti-TNF) therapy in ankylosing spondylitis. Rheumatology (Oxford) 2005 Oct; 44(10):1277-81.

(59) Dougados M, Dijkmans B, Khan M, Maksymowych W, van der Linden S, Brandt J. Conventional treatments for ankylosing spondylitis. Ann Rheum Dis 2002; 61 Suppl 3:iii40-50.

(60) Veale DJ, Ritchlin C, Fitzgerald O. Immunopathology of psoriasis and psoriatic arthritis. Ann Rheum Dis 2005; 64 Supp12:ii26-9.

(61) Braun J, Bollow M, Neure L, et al. Use of immunohistologic and in situ hybridization techniques in the examination of sacroiliac joint biopsy specimens from patients with ankylosing spondylitis. Arthritis Rheum 1995; 38:499-505.

(62) van der Heijde D, Dijkmans B, Geusens P, Sieper J, DeWoody K, Williamson P, Braun J. Ankylosing Spondylitis Study for the Evaluation of Recombinant Infliximab Therapy Study Group. Efficacy and safety of infliximab in patients with ankylosing spondylitis: results of a randomized, placebo-controlled trial (ASSERT). Arthritis Rheum 2005; 52:582-91.

(63) Davis JC, van der Heijde D, Braun J, Dougados M, Cush J, Clegg DO, et al. Recombinant human tumor necrosis factor receptor (etanercept) for treating ankylosing spondylitis: a randomized, controlled trial. Arthritis Rheum 2003; 48:3230-6.

(64) van der Heijde D, Kivitz A, Schiff M, Sieper J, Dijkmans B, Braun J, et al. Efficacy and safety of adalimumab in patients with ankylosing spondylitis: results of a multicenter, randomized, double-blind, placebo-controlled trial. Arthritis Rheum 2006; 54:2136-46.

(65) Rudwaleit M, Baeten D. Ankylosing spondylitis and bowel disease. Best Pract Res Clin Rheumatol 2006 Jun; 20(3):451-71.

(66) Braun J, Baraliakos X, Listing J, Sieper J. Decreased incidence of anterior uveitis in patients with ankylosing spondylitis treated with the anti-tumor necrosis factor agents infliximab and etanercept. Arthritis Rheum. 2005 Aug; 52(8):2447-51.

(67) Voulgari PV, Venetsanopoulou AI, Epagelis EK, Alamanos Y, Takalou I, Drosos AA. Infliximab in refractory psoriatic arthritis with severe psoriasis. A two-year experience. Ann Rheum Dis. 2006 Oct 26; [Epub ahead of print].

(68) Hanauer SB, Sandborn WJ, Rutgeerts P, Fedorak RN, Lukas M, MacIntosh D, Panaccione R, Wolf D, Pollack P. Human anti-tumor necrosis factor monoclonal antibody (adalimumab) in Crohn's disease: the CLASSIC-I trial. Gastroenterology. 2006 Feb; 130(2):323-33.

(69) Baraliakos X, Listing J, Brandt J, Alten R, et al. Persistent clinical efficacy and excellent safety over 5 years of treatment with the anti-TNFa agent infliximab in patients with ankylosing spondtlitis. Ann Rheum Dis 2006; 65 Supplii:206.

(70) Braun J, Sieper J, Geusens P, Dijkmans B, et al. Efficacy and safety on infliximab in patients with ankylosing spondylitis: 102 week results of the ASSERT trial. Ann Rheum Dis 2006; 65 Supplii:87.

(71) Davis JC, van der Heijde D, Braun J, et al. Sustained efficacy of etanercept in ankylosing spondylitis for up to 2 years. Ann Rheum Dis 2005; 64 Supplii.

(72) van der Heijde D, Kivitz A, Schiff M, Sieper J, Dijkmans B, Braun J, et al. Long-term adalimumab treatment reduces signs and symptoms in ankylosing spondylitis (AS) patients: results from the ATLAS trial. Ann Rheum Dis 2006; 65 Supplii:86

(73) Baraliakos X, Brandt J, Listing J, Haibel H, Sorensen H, Rudwaleit M, Sieper J, Braun J. Outcome of patients with active ankylosing spondylitis after two years of therapy with etanercept: clinical and magnetic resonance imaging data. Arthritis Rheum. 2005 Dec 15; 53(6):856-63.

(74) Sieper J, Baraliakos X, Listing J, Brandt J, Haibel H, Rudwaleit M, Braun J. Persistent reduction of spinal inflammation as assessed by magnetic resonance imaging in patients with ankylosing spondylitis after 2 yrs of treatment with the anti-tumour necrosis factor agent infliximab. Rheumatology (Oxford). 2005 Dec; 44(12):1525-30.

(75) Braun J, Landewe R, Hermann KG, Han J, Yan S, Williamson P, van der Heijde D; ASSERT Study Group. Major reduction in spinal inflammation in patients with ankylosing spondylitis after treatment with infliximab: results of a multicenter, randomized, double-blind, placebo-controlled magnetic resonance imaging study. Arthritis Rheum 2006 May; 54(5):1646-52

(76) Baraliakos X, Listing J, Rudwaleit M, Brandt J, Sieper J, Braun J. Radiographic progression in patients with ankylosing spondylitis after 2 years of treatment with the tumour necrosis factor alpha antibody infliximab. Ann Rheum Dis 2005; 64(10):1462-6.

(77) Baraliakos X, Listing J, Brandt J, Rudwaleit M, Sieper J, Braun J. Influence of Infliximab Therapy on Radiographic Progression in Patients with Ankylosing Spondylitis Results after 4 Years of Treatment. Arthritis Rheum 2005 Sep; 52(9): suppl.

(78) Rudwaleit M, Listing J, Brandt J, Braun J, Sieper J. Prediction of a major clinical response (BASDAI 50) to tumour necrosis factor alpha blockers in ankylosing spondylitis. Ann Rheum Dis 2004; 63:655-70.

(79) Keystone EC, safety issues related to emerging therapies for rheumatoid arthritis. Clin Exp Rheumatol 2004; 22:S148-50.

Saeed A. Shaikh, md, frcpc, facp *

* Assistant Professor, Department of Medicine, Division of Rheumatology, McMaster University, Hamilton, ON, Canada.

Contact information: Saeed A. Shaikh, 589 Lake Street, suite 204, St. Catharines, ON L2N 7L6, Tel: 905-937-2220, Fax: 905-937-4404.

Disclosures: the author has received consulting fees in the form of honouraria from Scherring, Abbott, and Amgen pharmaceuticals. The author has been involved in clinical studies with Scherring and Abbott pharmaceuticals. A grant was provided from Scherring for the preparation of this manuscript.
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Author:Shaikh, Saeed A.
Publication:Journal of the Canadian Chiropractic Association
Article Type:Report
Geographic Code:1CANA
Date:Oct 1, 2007
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