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 Table of Contents  
REVIEW ARTICLE
Year : 2020  |  Volume : 15  |  Issue : 5  |  Page : 34-39

Spectrum of spondyloarthritis


1 Department of Rheumatology, Tricolour Hospitals, Vadodara, Gujarat, India
2 Department of Rheumatology, Norfolk and Norwich University Hospital, Norwich, UK

Date of Web Publication23-May-2020

Correspondence Address:
Prof. Karl Gaffney
Consultant Rheumatologist, Norfolk and Norwich University Hospital, Norwich
UK
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0973-3698.284749

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  Abstract 


Spondyloarthritis (SpA) comprises a group of related diseases which share similar pathogenesis and clinical manifestations. Although the occurrence of SpA spectrum disorders has been known for some time, it was only in the latter half of the twentieth century that the concept of SpA was formally defined. Advances in radiography and magnetic resonance imaging techniques have led to the development of classification criteria which have aided early diagnosis and effective management. This narrative review summaries the latest developments in our understanding of the concept of SpA.

Keywords: Ankylosing spondylitis, axial spondyloarthritis, human leucocyte antigen-B27, nonradiographic axial spondyloarthritis, peripheral spondyloarthritis, psoriatic arthritis, reactive arthritis


How to cite this article:
Pathak H, Gaffney K. Spectrum of spondyloarthritis. Indian J Rheumatol 2020;15, Suppl S1:34-9

How to cite this URL:
Pathak H, Gaffney K. Spectrum of spondyloarthritis. Indian J Rheumatol [serial online] 2020 [cited 2020 Jun 3];15, Suppl S1:34-9. Available from: http://www.indianjrheumatol.com/text.asp?2020/15/5/34/284749




  Introduction Top


The concept of spondyloarthritis (SpA) and related conditions was first defined by Wright and Moll in 1976.[1] Our understanding of the SpA spectrum disorders has advanced significantly in the last decade, largely due to the availability of magnetic resonance imaging (MRI) and publication of the Assessment of Spondyloarthritis International Society (ASAS) classification criteria.[2],[3] SpA is an “umbrella term” for a heterogeneous group of diseases with shared genetic predisposition, pathogenic mechanisms, and clinical manifestations. Sacroiliitis, peripheral arthritis, enthesitis, dactylitis and extra-articular manifestations (EAMs) including acute anterior uveitis (AAU), psoriasis (Pso), and inflammatory bowel diseases (IBDs) are prototypical manifestations of SpA. Late recognition of these features in the disease course contributes to delayed diagnosis, resulting in worse functional outcomes, spinal and peripheral joint damage, and an attenuated response to biological therapy.[4]


  Pathogenesis of Spondyloarthritis Top


The pathological hallmarks of SpA are enthesitis and osteitis, and there is a strong genetic association with inheritance of the human leukocyte antigen (HLA)-B27 gene, an allele of the major histocompatibility (MHC) gene complex. HLA-B27 is a surface antigen encoded by the B-locus of MHC class I gene (class I HLA in humans). The prevalence of HLA-B27 in the general population is approximately 6%–10%; however, it is present in between 74% and 89% of SpA patients – the highest association being in ankylosing spondylitis (AS).[5] The function of MHC class I molecules is to present endogenous peptides to the cytotoxic CD8+ T-cell through T-cell receptors on the cell surface. Dysregulation of antigen presentation through HLA-B27 leads to impaired T-cell responses, alteration of regulatory T-cell function, and enhanced apoptotic death. Immune dysregulation at entheseal and intestinal barrier membranes is considered to be the primary site of activation of the immune cascade. In a mouse model, it has been shown that entheseal CD4+ and CD8+ T-cells, in association with interleukin (IL)-23, produce pro-inflammatory cytokines including IL-17. These along with non-MHC dysfunctions of molecules such as endoplasmic reticulum aminopeptidase (ERAP)-1 result in pro-inflammatory cytokines generation, leading to enthesopathy, joint erosions, and osteoproliferation.[5],[6]


  Spectrum of Spondyloarthritis Top


SpA encompasses the following disorders [Figure 1]:
Figure 1: Unified concept of spondyloarthritis

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  • Axial SpA (AS [also known as radiographic SpA] and nonradiographic SpA)
  • Psoriatic arthritis
  • IBD-related arthritis
  • Reactive arthritis (ReA)
  • Peripheral SpA.


There may be patient subsets who cannot be clearly categorized within this spectrum. These patients might be early in the course of disease evolution and develop a typical spectrum in later years. However, some patients remain unclassifiable and therefore may be labeled as undifferentiated SpA.


  Axial Spondyloarthritis Top


The term axial spondyloarthritis (axSpA) comprises a heterogeneous group of diseases with AS as its prototype but also includes nonradiographic axSpA (nr-axSpA). Patients with axSpA typically describe inflammatory back pain (IBP) which is usually characterized by at least four of the following features: age of onset <45 years; duration >3 months; morning back stiffness ≥30 min and pain which improves with exercise but not with rest; and second half of nighttime awakening due to back pain and alternating buttock pain.[7]

The diagnosis of AS requires an evidence of bilateral grade 2 or unilateral grade 3 or 4 sacroiliitis on radiograph.[8] We know that the disease starts long before structural changes including sclerosis, erosions, and ankylosis is visible on radiographs of the spine and sacroiliac joints. Our understanding of axSpA has improved significantly in the past two decades, driven by advances in imaging, development of new classification criteria, and the availability of new effective biological therapies. It has long been recognized that there are a cohort of patients with the AS clinical phenotype, but in whom radiographs may be normal, resulting in a considerably delayed or incorrect diagnosis.[9] In 2009, the concept of nr-axSpA was proposed by ASAS, enabling patients to be classified with axSpA without the requirement for X-ray evidence of structural damage.[2] Utilizing these criteria, patients can be classified utilizing MRI and/or a number of clinical criteria if they are positive for HLA-B27. Although these classification criteria were originally intended for epidemiology and clinical research purposes, they facilitate earlier diagnosis and inform treatment decisions [Figure 2]. Research during the past two decades has repeatedly validated the concept of nr-axSpA as a part of the SpA spectrum, and it can be expected that between 23% and 80% patients may have nr-axSpA at the time of new diagnosis of axSpA.[8] Similarly, radiographic sacroiliitis may be present in 20%–30% axSpA at the time of diagnosis with 2–3 years of symptoms.[10]
Figure 2: Assessment of Spondyloarthritis International Society Classification Criteria for axial spondyloarthritis

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Comparison between AS and nr-axSpA is discussed in [Table 1].[11],[12] AS is more common in men and more strongly associated with HLA-B-27. Not all patients with nr-axSpA progress to AS. It is been postulated that about 10% of nr-axSpA patients, diagnosed by clinical and radiographical criteria, will progress into radiographic axSpA within 2 years.[12] The presence of a raised baseline CRP and active sacroiliitis on MRI increases this risk. This suggests that the progression from the nonradiographic phase to radiographic is not linear or indeed inevitable.[12]
Table 1: Comparison between nonradiographic axial spondyloarthritis and ankylosing spondylitis

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Peripheral musculoskeletal manifestations include arthritis, enthesitis, and dactylitis. Peripheral arthritis predominantly involves the lower limb joints: ankles, hips, and knees; however, the shoulders and sternoclavicular joints can also be affected. In a meta-analysis of eight studies of axSpA patients, the pooled prevalences of peripheral arthritis, enthesitis, and dactylitis were 29.7%, 28.8%, and 6%, respectively, and occurrence was similar in AS and nr-axSpA.[11] In the DESIR cohort, the presence of AAU, smoking, and HLA-B27 positivity was associated with less peripheral arthritis among patients with axSpA.[12] Common sites of entheseal inflammation include the Achilles tendon, plantar fascia, lateral and medial epicondyles, shoulders, iliac crest, costochondral joints, costovertebral joints, and vertebras. Dactylitis is present in approximately 6% of axSpA patients.[11]

AAU, Pso, and IBD are referred to as EAM of SpA. The occurrence of EAMs is influenced by genetic predisposition and environmental factors. AAU is the most common EAM of axSpA and its prevalence increases with disease duration. Undiagnosed AAU can cause visual loss in SpA patients. The prevalence of AAU is higher in AS (23.0%) than nr-axSpA (15.9%); however, other peripheral articular and EAMs were similar in AS and nr-axSpA.[11],[13] AAU can also be seen in with PsA (7%–19%) and IBD (2%).[14] Approximately 50% of AAU patients are HLA-B27 positive, and unilateral uveitis is the more common presentation.[14] Increased expression of HLA-B27 and vascular adhesion molecules on uveal connective tissues, mechanical stress on intraocular entheses, endoplasmic reticulum dysregulation, and increased propensity to infections are a few of the proposed mechanisms for AAU in SpA.[14]


  Psoriatic Arthritis Top


Psoriatic arthritis was considered to be a subset of rheumatoid arthritis in the earlier part of the 20th century; however, epidemiological studies have shown that PsA is a distinct clinical entity. The American College of Rheumatology first included PsA in the classification of rheumatic diseases in 1963. In 1973, Moll and Wright described five clinical subtypes of PsA: predominant distal interphalangeal joint disease, asymmetrical oligoarthritis, symmetrical polyarthritis (resembling rheumatoid arthritis in appearance), spondylitis, and arthritis mutilans. They also proposed criteria for establishing a diagnosis of PsA, based on the presence of inflammatory arthritis in a Pso patient who had a negative rheumatoid factor.[15] Although these criteria were capable of recognizing PsA in patients with established Pso and arthritis, this classification of PsA could exclude patients with Pso and predominant enthesitis and dactylitis. In 2006, an international collaborative effort led to the development off the CASPAR criteria, which are highly sensitive (91.4%) and highly specific (98.7%) for a diagnosis of PsA [Table 2].[16] PsA is associated with class I MHC alleles. The IL-17/23 and tumor necrosis factor pathways play a key role in pathogenesis. HLA-B*08, B*27, B*38, and B*39 have been associated with PsA. The prevalence of HLA-B27 in PsA is between 45% and 50%.[17],[18],[19]
Table 2: CASPER criteria

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Peripheral arthritis is more common in PsA with axial involvement than in AS.[20],[21] Enthesitis can manifest in approximately 80% of PsA patients. Dactylitis is seen in up to 30% and is most common in the toes but can occur in any digit. Between 30% and 50% of patients have oligoarthritis, and in approximately 15% of cases, arthritis can precede Pso.[17],[18] Younger age of disease onset, male, HLA-B27 positivity, nail dystrophy, raised inflammatory markers, and peripheral joint damage are risk factors for the development of axial disease in PsA patients.[19] Axial involvement in PsA has long been recognized and manifests on MRI and/or X-ray as sacroiliitis and/or spinal involvement. Typical spinal lesions include vertebral corner lesions, squaring of vertebrae, sclerosis, syndesmophytes (marginal and para-marginal), discitis, facet joint arthritis, atlantoaxial subluxation, and paravertebral ossification.[20],[21]

IBP is reported in 15%–19% of PsA cohorts and about one-third of patients with PsA may have asymptomatic sacroiliitis on imaging which is more common in women.[20] The presence of HLA-B27 in PsA is associated with bilateral sacroiliitis and AS like vertebral changes. However, there are some significant radiographic differences in spinal disease between axSpA and PsA. Psoriatic sacroiliitis is asymmetrical/unilateral; syndesmophytes are less common but bulkier, may not exactly follow the course of the anterior longitudinal ligament and affect vertebrae intermittently rather than in a stepwise fashion. Due to less apophyseal joint involvement, spinal movements are less restricted in PsA.[20],[21] This information suggests that axial PsA is a different disease than AS with Pso.[21]


  Reactive Arthritis Top


ReA is defined as arthritis developing after extra-articular infection where a pathogen cannot be isolated from the affected joints. ReA is characterized by asymmetrical oligoarthritis, predominantly affecting the lower limb joints, unilateral or bilateral sacroiliitis, dactylitis, and enthesitis. The characteristic EAMs are elucidated in [Table 3]. Reiter's syndrome is a variant of ReA, first described by Hans Reiter as a triad of oligoarthritis, urethritis, and conjunctivitis in a young officer with “treponema arthritides.”[22] Aphthous ulcers in the mouth, erythema nodosum, conjunctivitis, and keratoderma blennorrhagica are EAMs associated with ReA. Keratoderma blennorrhagica, a distinctive skin rash presents on the soles and palms, is the characteristic dermatological manifestation of ReA. Clinically and histopathologically, the rash is similar to Pso. In uncircumcised males, circinate balanitis may also be seen on the glans penis.[23]
Table 3: Clinical manifestations of reactive arthritis

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Often, it can be difficult to differentiate ReA from other members of the SpA spectrum; however, early recognition of the association with recent genitourinary or gastrointestinal infections in ReA usually helps to establish the correct diagnosis. Diarrhea or urethritis for at least 1-day, 3 days to 6 weeks prior to arthritis development is considered significant.[23] The infection activates the local immune response at the site (synovial membranes). The main bacteria involved are Campylobacter, Chlamydia,  Salmonella More Details, Shigella, and  Yersinia More Details [Table 4]. Although causative bacteria are not cultured from the joints, lipopolysachhride and heat shock protein antigens from the enteric bacterial membrane coating have been found in the affected joints of ReA patients. Chlamydial DNA has also been found from synovial fluids of ReA patients' posturethrogenital infections.[23]
Table 4: Causative organisms associated with reactive arthritis

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The prevalence of ReA in HLA-B27 positive patients is five times higher than the general population, and in HLA-B27 positive relatives of ReA patients, the prevalence is another ten times higher.[24] Poststreptococcal, Lyme, and viral arthritis are different entities, not HLA-B27 associated, and should be described as distinct entities under the general heading of infection-related arthritis.[23]


  Inflammatory Bowel Disease-related Arthritis Top


The prevalence of asymptomatic sacroiliitis in IBD (Crohn's diseases and ulcerative colitis) is between 11% and 52%, and approximately 10% of patients develop typical AS.[25] Conversely, approximately 6.5% of AS patients can develop IBD as an EAMs.[26] IBD-related arthritis is more common in Crohn's disease, and usually, its course is independent of IBD disease activity status. The pathogenesis of IBD related arthritis is a complex interaction between host genetic predisposition (HLA B27, ERAP1, and other non-MHC factors), and the gut microbiome leading to decreased Treg cells and activation of T helper 17 cells and the IL-17/23 pathway.[25],[26] Increased intestinal permeability and immune cell migration with activated intestinal lymphocytes mediating peripheral synovitis are other proposed models of the gut-joint inflammatory axis. This is the subject of considerable ongoing research.[14],[26]

Arthropathy in IBD is divided into peripheral and axial arthritis. Peripheral arthritis can be oligo-articular (<5 joints) asymmetrical arthritis (Type 1) involving the large joints of upper and lower limbs or bilaterally symmetrical small joint arthritis (>5 joints, Type 2). The Type 1 arthritis is usually transient, migratory, and self-limiting without deformity in 6–10 weeks. Type 2 arthritis can be symptomatic for months to years.[26] Other SpA features including enthesitis and dactylitis can be seen in 2%–10% of IBD patients.[14] Axial disease can present as IBP, isolated sacroiliitis, or AS.[25]


  Peripheral Spondyloarthritis Top


Patients having predominant asymmetrical lower limb arthritis or enthesitis or dactylitis who do not fulfil criteria of any of the other SpA spectrum of diseases can be classified as peripheral SpA in the presence of other pertinent SpA features [Figure 3].[3] The presence of Pso, absence of HLA-B27, and older age were associated with more peripheral SpA.[27] It is important to understand that patients with predominant axial involvement (AS and nr-axSpA) with few peripheral features should not be categorized as peripheral SpA [Figure 4]. It should be emphasized that classification criteria are intended to increase the homogeneity of patient cohorts in clinical trials and epidemiology studies. There may be considerable overlap of peripheral SpA with other SpA spectrum conditions in real-life scenarios. In those situations, authors recommend modifying management strategies according to the manifestations present at the time of clinical review.
Figure 3: Classification of peripheral spondyloarthritis

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Figure 4: Axial spondyloarthritis vs peripheral spondyloarthritis

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  Conclusion Top


Recent research has improved our understanding of SpA spectrum disorders. The insight into immunopathogenic mechanisms and the development of validated disease classification criteria have facilitated a successful clinical trial program, which has helped establish new and effective therapies. There is an urgent need to increase awareness of SpA spectrum disorders among primary care physicians and other medical specialties to shorten the time to diagnosis and allow access to effective therapy.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Wright V, Moll JM, editors. Seronegative Polyarthritis. Amsterdam: North Holland Publishing; 1976.  Back to cited text no. 1
    
2.
Rudwaleit M, van der Heijde D, Landewé R, Listing J, Akkoc N, Brandt J, et al. The development of Assessment of SpondyloArthritis international Society classification criteria for axial spondyloarthritis (part II): Validation and final selection. Ann Rheum Dis 2009;68:777-83.  Back to cited text no. 2
    
3.
Rudwaleit M, van der Heijde D, Landewé R, Akkoc N, Brandt J, Chou CT, et al. The Assessment of SpondyloArthritis International Society classification criteria for peripheral spondyloarthritis and for spondyloarthritis in general. Ann Rheum Dis 2011;70:25-31.  Back to cited text no. 3
    
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van Tubergen A, Weber U. Diagnosis and classification in spondyloarthritis: Identifying a chameleon. Nat Rev Rheumatol 2012;8:253-61.  Back to cited text no. 4
    
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Taurog JD, Chhabra A, Colbert RA. Ankylosing spondylitis and axial spondyloarthritis. N Engl J Med 2016;374:2563-74.  Back to cited text no. 5
    
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Furst DE, Louie JS. Targeting inflammatory pathways in axial spondyloarthritis. Arthritis Res Ther 2019;21:135.  Back to cited text no. 6
    
7.
Sieper J, van der Heijde D, Landewé R, Brandt J, Burgos-Vagas R, Collantes-Estevez E, et al. New criteria for inflammatory back pain in patients with chronic back pain: A real patient exercise by experts from the Assessment of SpondyloArthritis international Society (ASAS). Ann Rheum Dis 2009;68:784-8.  Back to cited text no. 7
    
8.
van der Linden S, Valkenburg HA, Cats A. Evaluation of diagnostic criteria for ankylosing spondylitis. A proposal for modification of the New York criteria. Arthritis Rheum 1984;27:361-8.  Back to cited text no. 8
    
9.
Rudwaleit M, Khan MA, Sieper J. The challenge of diagnosis and classification in early ankylosing spondylitis: Do we need new criteria? Arthritis Rheum 2005;52:1000-8.  Back to cited text no. 9
    
10.
Sieper J, van der Heijde D. Review: Nonradiographic axial spondyloarthritis: New definition of an old disease? Arthritis Rheum 2013;65:543-51.  Back to cited text no. 10
    
11.
de Winter JJ, van Mens LJ, van der Heijde D, Landewé R, Baeten DL. Prevalence of peripheral and extra-articular disease in ankylosing spondylitis versus non-radiographic axial spondyloarthritis: A meta-analysis. Arthritis Res Ther 2016;18:196.  Back to cited text no. 11
    
12.
López-Medina C, Dougados M, Ruyssen-Witrand A, Moltó A. Evaluation of concomitant peripheral arthritis in patients with recent onset axial spondyloarthritis: 5-year results from the DESIR cohort. Arthritis Res Ther 2019;21:139.  Back to cited text no. 12
    
13.
Baraliakos X, Braun J. Non-radiographic axial spondyloarthritis and ankylosing spondylitis: What are the similarities and differences? RMD Open 2015;1:e000053.  Back to cited text no. 13
    
14.
Rosenbaum JT, Asquith M. The microbiome and HLA-B27-associated acute anterior uveitis. Nat Rev Rheumatol 2018;14:704-13.  Back to cited text no. 14
    
15.
Moll JM, Wright V. Psoriatic arthritis. Semin Arthritis Rheum 1973;3:55-78.  Back to cited text no. 15
    
16.
Taylor W, Gladman D, Helliwell P, Marchesoni A, Mease P, Mielants H, et al. Classification criteria for psoriatic arthritis: Development of new criteria from a large international study. Arthritis Rheum 2006;54:2665-73.  Back to cited text no. 16
    
17.
FitzGerald O, Haroon M, Giles JT, Winchester R. Concepts of pathogenesis in psoriatic arthritis: Genotype determines clinical phenotype. Arthritis Res Ther 2015;17:115.  Back to cited text no. 17
    
18.
Coates LC, FitzGerald O, Helliwell PS, Paul C. Psoriasis, psoriatic arthritis, and rheumatoid arthritis: Is all inflammation the same? Semin Arthritis Rheum 2016;46:291-304.  Back to cited text no. 18
    
19.
Ritchlin CT, Colbert RA, Gladman DD. Psoriatic Arthritis. N Engl J Med 2017;376:957-70.  Back to cited text no. 19
    
20.
Baraliakos X, Coates LC, Braun J. The involvement of the spine in psoriatic arthritis. Clin Exp Rheumatol 2015;33:S31-5.  Back to cited text no. 20
    
21.
Feld J, Ye JY, Chandran V, Inman RD, Haroon N, Cook R, et al. Is axial psoriatic arthritis distinct from ankylosing spondylitis with and without concomitant psoriasis? Rheumatology (Oxford, England). 2019. DOI: 10.1093/rheumatology/kez457.  Back to cited text no. 21
    
22.
Reiter H. Uber eine bisher unerkannte spirochaten infection. Dtsch Med Wochenschr 1916;42:1535-6.   Back to cited text no. 22
    
23.
Selmi C, Gershwin ME. Diagnosis and classification of reactive arthritis. Autoimmun Rev 2014;13:546-9.  Back to cited text no. 23
    
24.
Colmegna I, Cuchacovich R, Espinoza LR. HLA-B27-associated reactive arthritis: Pathogenetic and clinical considerations. Clin Microbiol Rev 2004;17:348-69.  Back to cited text no. 24
    
25.
Jacques P, Van Praet L, Carron P, Van den Bosch F, Elewaut D. Pathophysiology and role of the gastrointestinal system in spondyloarthritides. Rheum Dis Clin North Am 2012;38:569-82.  Back to cited text no. 25
    
26.
Brakenhoff LK, van der Heijde DM, Hommes DW, Huizinga TW, Fidder HH. The joint-gut axis in inflammatory bowel diseases. J Crohns Colitis 2010;4:257-68.  Back to cited text no. 26
    
27.
López-Medina C, Moltó A, Dougados M. Peripheral manifestations in spondyloarthritis and their effect: an ancillary analysis of the ASAS-COMOSPA study. The Journal of Rheumatology 2020;47:211-7.  Back to cited text no. 27
    


    Figures

  [Figure 1], [Figure 2], [Figure 3], [Figure 4]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]



 

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Abstract
Introduction
Pathogenesis of ...
Spectrum of Spon...
Axial Spondyloar...
Psoriatic Arthritis
Reactive Arthritis
Inflammatory Bow...
Peripheral Spond...
Conclusion
References
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