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Irene van der Horst-Bruinsma, Mirjam de Vries,
Filip Van den Bosch
A previous version was co-authored by Joachim Sieper, Hildrun Haibel, Herman
Mielants and Philippe Carron
IN-DEPTH DISCUSSION II
Choice of TNF blocking agents in relation to extra-
articular manifestations in Spondyloarthritis
Management of
spondyloarthritides
EULAR on-line course on Rheumatic Diseases
Management of spondyloarthritides – Module 7
Spondyloarthritis (SpA) is a chronic inflammatory disease with either predominant axial symptoms of the spine
and sacroiliac joints (axial SpA, including ankylosing spondylitis) or predominant peripheral manifestations,
such as arthritis, enthesitis, or dactylitis (peripheral SpA). Next to these spinal and articular symptoms, many
patients with SpA also suffer from extra-articular manifestations (EAMs).
Spondyloarthritis-concept related EAMs include anterior uveitis (25-30%), psoriasis (10-25%) or inflammatory
bowel disease (IBD) (5-10%). The treatments, used for the rheumatological manifestations of the disease, such
as NSAIDs, DMARDs and TNF-blocking agents may have a differential effect on these EAMs, and therefore the
presence of these manifestations should be taken into account when taking therapeutic decisions.
Uveitis.
Acute anterior uveitis is an acute attack with inflammation of the uvea and can be the first presenting
symptom of the disease. In a study among 433 patients with different types of uveitis, 44 cases (almost 10%)
of SpA were detected, whereas others showed a percentage up to 50% of previously undiagnosed cases of SpA
among uveitis patients (1-3).
The occurrence of acute anterior uveitis is increased in the HLA-B27 positive population, with a lifetime
cumulative incidence of 0.2 % in the general population compared with 1% in the HLA-B27 positive population
(4).
The attacks of uveitis are usually recurrent and unilateral. The symptoms are sudden ocular pain with redness
and photophobia. Inflammation can lead to debris, which accumulates in the anterior chamber and may cause
papillary and lens dysfunction with blurring of vision. In some cases glaucoma and severe visual impairment
occurs if adequate treatment is delayed, but most of the time, with local treatment, the uveitis subsides
spontaneously within 3 months. In SpA patients with sudden symptoms of a painful, red eye, it is
recommended to refer the patient to the ophthalmologist as soon as possible.
In most cases acute uveitis can be successfully treated by the ophthalmologist with local corticosteroids and
mydriatics. Sometimes high oral dosage of prednisone (up to 60 mg daily) is necessary to control
inflammation. In most cases there is no residual visual impairment.
Some data suggest that continuous use of NSAID’s show efficacy for uveitis flares. There is some evidence that
the use of sulfasalazine reduces the recurrence rate of uveitis (5, 6). Other immunosuppressive drugs used by
the ophthalmologists to treat refractory uveitis, such as azathioprine and methotrexate, do not have much
efficacy on the disease activity of SpA.
Some TNF-blocking agents, can be used for both indications, active disease of SpA as well as refractory uveitis.
Infliximab is an adequate treatment of SpA, decreases the recurrence rate of uveitis and is effective in
2©2007-2014 EULAR
Management of spondyloarthritides – Module 7
refractory uveitis (7, 8). The efficacy of etanercept, on uveitis is doubted, as etanercept does not seem to
prevent a relapse in combination with methotrexate (9) and it was suggested that etanercept might even
trigger an attack of uveitis (10). However, a comparison of three randomised studies with etanercept in AS
showed a lower number of cases with uveitis in the etanercept-treated patients compared with placebo (11)
indicating that etanercept inhibits the recurrence of uveitis.
An analysis of 4 placebo-controlled studies and 3 open-label studies with TNF agents in AS showed a frequency
of flares of anterior uveitis in the placebo-group of 15.6 per 100 patient-years, compared with 7.9 per 100
patient-years in etanercept group and 3.4 per 100 patient-years in the infliximab treated patients (8). The
attacks of uveitis during these studies were reported by the patients and no follow up studies or
ophthalmologic controls were performed.
Reports on the efficacy of adalimumab on uveitis are mainly based on retrospective analysis of placebo
controlled trials which show beneficial results (12). In a prospective study, AS patients were treated with
adalimumab because of their high disease activity and screened by an ophthalmologist on uveitis as well. This
study demonstrates a significant decrease (73%) of the recurrence rate of uveitis (13) during adalimumab
treatment.
Data on the efficacy of golimumab and certolizumab on the recurrence rate of anterior uveitis are lacking so
far.
It can be concluded that in most cases, attacks of anterior uveitis respond very well to (local) treatment by the
ophthalmologist. In cases with refractory uveitis or a high uveitis recurrence rate, treatment with TNF blocking
agents can be successful, especially if the treatment is indicated for high disease activity of SpA. Adalimumab
and infliximab seem to be more effective in lowering the recurrence rate of uveitis compared to etanercept.
Psoriasis
Psoriasis is a common skin disease with plaque lesions and nail deformities and is primarily treated by the
dermatologist. Psoriatic arthritis occurs in 5-20% of the people with psoriasis and can present as a symmetrical
polyarthritis, resembling rheumatoid arthritis, but with additional involvement of the DIP-joints (14). Axial
disease occurs in about 5% of the psoriasis patients with asymmetrical sacroiliitis in one-third of the cases and
spondylitis without sacroiliitis in the rest. Enthesitis and dactylitis are common, especially in the oligoarticular
form of the disease. In SpA, patients with psoriatic arthritis excluded, psoriasis occurs in approximately 5-10%.
In case of scaling skin lesions or nail changes suspicious for psoriasis in SpA it is recommended to refer the
patients to a dermatologist.
Skin manifestations of psoriasis usually respond very well to local corticosteroids or PUVA therapy.
3©2007-2014 EULAR
Management of spondyloarthritides – Module 7
In case of psoriatic arthritis, NSAID’s and intra-articular injections with corticosteroid are effective in mono-or
oligoarthritis (15). Methotrexate is proven to be effective in daily clinical practice for treating the skin and
oligo- and polyarthritis, despite the lack of randomized controlled trails to support this (15, 30).). Leflunomide
is also effective in both psoriasis and peripheral arthritis, but not on the axial manifestations of SpA (16).
TNF alfa blockers, such as infliximab, etanercept, adalimumab, certolizumab and golimumab are efficacious on
the skin and nail lesions of psoriasis (15). In some cases treatment of SpA with TNF blocking agents can result
in a new manifestations of psoriasis, such as palmoplantarpustulosis (17).
Inflammatory Bowel Disease
Inflammatory Bowel disease includes Crohn’s disease and ulcerative colitis and is primarily treated by the
gastro-enterologist. Approximately 10% of the IBD patients develop SpA. On the other hand, the chance of SpA
patients to develop IBD is 5-10%. Asymptomatic inflammatory bowel disease is described in a high percentage
of SpA patients (60%) and can be detected by endoscopy of the colon and terminal ileum (18). During follow
up studies it appeared that up to 20% of the SpA patients with chronic gut inflammation eventually develop
Crohn’s disease (19).
Another indication that diseases as SpA and IBD show some overlap is a study on serological markers of IBD. In
this study, a high percentage (55%) of AS patients without abdominal complaints had a positive tests for
pANCA, ANCA or Omp-C ASCA antibodies (20).
In case of persistent or frequently recurring diarrhoea and/or blood or mucus production with the stools it is
advised to refer the SpA patients to the gastro-enterologist in order to perform a colonoscopy.
Treatment of IBD by the gastro-enterologist is based on immunosuppressive drugs and anti-TNF. The use of
NSAID’s can worsen the colitis manifestations, therefore it is advised to minimise the use of these drugs by
SpA patients with IBD, except for celecoxib which does not seem to increase the risk at exacerbation of the IBD
(21). The use of sulfasalazine can be beneficial for both SpA as well as IBD. The efficacy of other
immunosuppressive drugs often used in IBD however, have in most cases not proven efficacy in SpA (22). Of
the TNF blocking agents only infliximab and adalimumab are effective in SpA as well as IBD and golimumab is
not yet registered for IBD but shows efficacy in ulcerative colitis (23-28). Certolizumab is also effective in IBD
but not yet registered in all countries for this indication.
Etanercept works well for spinal symptoms in SpA but not on IBD and new manifestations of IBD might even
occur during etanercept treatment (28, 29).
4©2007-2014 EULAR
Management of spondyloarthritides – Module 7
Therefore, in SpA patients with IBD the use of NSAID’s should be minimised, except for celecoxib, sulfasalazine
might show some improvement for both indications and the first choice of anti-TNF is infliximab or
adalimumab.
Conclusions
In SpA physical exercises and NSAID’s are the choice of treatment. In case of peripheral arthritis,
sulphasalazine can be added as a useful DMARD.
In case of insufficient response at NSAID’s TNF blockers are very effective in SpA, especially infliximab,
etanercept, adalimumab, certolizumab and golimumab. These drugs all work very well on the axial
manifestations as well as on arthritis, enthesitis and psoriasis.
Concerning the treatment of other extra spinal manifestations, anterior uveitis can be treated adequately by
the ophthalmologist with local treatment. In refractory uveitis or a high recurrence rate, treatment with
adalimumab and infliximab seem to be more effective for this indication compared to etanercept.
In case of IBD in SpA, the use of NSAID’s should be minimized but celecoxib can be used if needed. The choice
of anti-TNF therapy inSpA with IBD is in favour of infliximab and adalimumab instead of etanercept.
Overall, it is important to realize that in SpA extra-articular manifestations do occur frequently and should be
taken into account in the choice of treatment,
5©2007-2014 EULAR
Management of spondyloarthritides – Module 7
References
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Rheumatol. 2004 Nov;31(11):2226-9.
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extraocular manifestations in patients with HLA-B27 uveitis: a study of 175 cases. Ophthalmology.
2004;111(4):802-9.
3. Pato E, Banares A, Jover JA, Fernandez-Gutierrez B, Godoy F, Morado C, Mendez R, Hernandez-Garcia
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4. Linssen A, Rothova A, Valkenburg HA, Dekker-Saeys AJ, et al.The lifetime cumulative incidence of acute
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interim analysis. ClinExp Rheumatology 2010;28:630
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Weinblatt ME Weisman MH. Mosby, Edinburg. 2003, vol 2.1161-1181
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Management of spondyloarthritides – Module 7
15. Gossec L, Smolen JS, Gaujoux-Viala C, Ash Z, Marzo-Ortega H, van der Heijde D, FitzGerald O, Aletaha
D, Balint P, Boumpas D, Braun J, Breedveld FC, Burmester G, Cañete JD, de Wit M, Dagfinrud H, de Vlam K,
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McInnes IB, Ritchlin C, Sieper J, Tak PP, Valesini G, Vencovsky J, Winthrop KL, Zink A, Emery P; European
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psoriatic arthritis: an in-depth analysis of data from the TOPAS study. Dermatology. 2006;212(3):238-49
17. Kary S, Worm M, Audring H, Huscher D, Renelt M, Sorensen H, Stander E, Maass U, Lee H, Sterry W,
Burmester GR. New onset or exacerbation of psoriatic skin lesions in patients with definite rheumatoid
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spondyloarthropathies: clinical, radiologic, biologic, and genetic features in relation to the type of histology. A
prospective study. J Rheumatol. 1991;18(10):1542-51
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Ratnawati H, Dijkmans B. pANCA, ASCA, and OmpC antibodies in patients with ankylosing spondylitis without
inflammatory bowel disease. J Rheumatol. 2010 Nov;37(11):2340-4.
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celecoxib in patients with ulcerative colitis in remission: a randomized, placebo-controlled, pilot study.
ClinGastroenterolHepatol. 2006 Feb;4(2):203-11
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modifying antirheumatic drugs. ClinExp Rheumatology 2002;20:S67-S70.
23. Braun J, Baraliakos X, Listing J, Davis J, van der Heijde D, Haibel H, Rudwaleit M, Sieper J. Differences in
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exposed to therapy with anti-tumor necrosis factor alpha agents.Arthritis Rheum. 2007 May 15;57(4):639-47.
24. Hanauer SB, Feagan BG, Lichtenstein GR, Mayer LF, Schreiber S, Colombel JF, Rachmilewitz D, Wolf DC,
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randomised trial. Lancet. 2002 May 4;359(9317):1541-9.
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7©2007-2014 EULAR
Management of spondyloarthritides – Module 7
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Kent JD, Bittle B, Li J, Pollack PF. Adalimumab for maintenance treatment of Crohn's disease: results of the
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8©2007-2014 EULAR

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Choice of TNF b. for extra-articular manifestations in SpA

  • 1. Irene van der Horst-Bruinsma, Mirjam de Vries, Filip Van den Bosch A previous version was co-authored by Joachim Sieper, Hildrun Haibel, Herman Mielants and Philippe Carron IN-DEPTH DISCUSSION II Choice of TNF blocking agents in relation to extra- articular manifestations in Spondyloarthritis Management of spondyloarthritides EULAR on-line course on Rheumatic Diseases
  • 2. Management of spondyloarthritides – Module 7 Spondyloarthritis (SpA) is a chronic inflammatory disease with either predominant axial symptoms of the spine and sacroiliac joints (axial SpA, including ankylosing spondylitis) or predominant peripheral manifestations, such as arthritis, enthesitis, or dactylitis (peripheral SpA). Next to these spinal and articular symptoms, many patients with SpA also suffer from extra-articular manifestations (EAMs). Spondyloarthritis-concept related EAMs include anterior uveitis (25-30%), psoriasis (10-25%) or inflammatory bowel disease (IBD) (5-10%). The treatments, used for the rheumatological manifestations of the disease, such as NSAIDs, DMARDs and TNF-blocking agents may have a differential effect on these EAMs, and therefore the presence of these manifestations should be taken into account when taking therapeutic decisions. Uveitis. Acute anterior uveitis is an acute attack with inflammation of the uvea and can be the first presenting symptom of the disease. In a study among 433 patients with different types of uveitis, 44 cases (almost 10%) of SpA were detected, whereas others showed a percentage up to 50% of previously undiagnosed cases of SpA among uveitis patients (1-3). The occurrence of acute anterior uveitis is increased in the HLA-B27 positive population, with a lifetime cumulative incidence of 0.2 % in the general population compared with 1% in the HLA-B27 positive population (4). The attacks of uveitis are usually recurrent and unilateral. The symptoms are sudden ocular pain with redness and photophobia. Inflammation can lead to debris, which accumulates in the anterior chamber and may cause papillary and lens dysfunction with blurring of vision. In some cases glaucoma and severe visual impairment occurs if adequate treatment is delayed, but most of the time, with local treatment, the uveitis subsides spontaneously within 3 months. In SpA patients with sudden symptoms of a painful, red eye, it is recommended to refer the patient to the ophthalmologist as soon as possible. In most cases acute uveitis can be successfully treated by the ophthalmologist with local corticosteroids and mydriatics. Sometimes high oral dosage of prednisone (up to 60 mg daily) is necessary to control inflammation. In most cases there is no residual visual impairment. Some data suggest that continuous use of NSAID’s show efficacy for uveitis flares. There is some evidence that the use of sulfasalazine reduces the recurrence rate of uveitis (5, 6). Other immunosuppressive drugs used by the ophthalmologists to treat refractory uveitis, such as azathioprine and methotrexate, do not have much efficacy on the disease activity of SpA. Some TNF-blocking agents, can be used for both indications, active disease of SpA as well as refractory uveitis. Infliximab is an adequate treatment of SpA, decreases the recurrence rate of uveitis and is effective in 2©2007-2014 EULAR
  • 3. Management of spondyloarthritides – Module 7 refractory uveitis (7, 8). The efficacy of etanercept, on uveitis is doubted, as etanercept does not seem to prevent a relapse in combination with methotrexate (9) and it was suggested that etanercept might even trigger an attack of uveitis (10). However, a comparison of three randomised studies with etanercept in AS showed a lower number of cases with uveitis in the etanercept-treated patients compared with placebo (11) indicating that etanercept inhibits the recurrence of uveitis. An analysis of 4 placebo-controlled studies and 3 open-label studies with TNF agents in AS showed a frequency of flares of anterior uveitis in the placebo-group of 15.6 per 100 patient-years, compared with 7.9 per 100 patient-years in etanercept group and 3.4 per 100 patient-years in the infliximab treated patients (8). The attacks of uveitis during these studies were reported by the patients and no follow up studies or ophthalmologic controls were performed. Reports on the efficacy of adalimumab on uveitis are mainly based on retrospective analysis of placebo controlled trials which show beneficial results (12). In a prospective study, AS patients were treated with adalimumab because of their high disease activity and screened by an ophthalmologist on uveitis as well. This study demonstrates a significant decrease (73%) of the recurrence rate of uveitis (13) during adalimumab treatment. Data on the efficacy of golimumab and certolizumab on the recurrence rate of anterior uveitis are lacking so far. It can be concluded that in most cases, attacks of anterior uveitis respond very well to (local) treatment by the ophthalmologist. In cases with refractory uveitis or a high uveitis recurrence rate, treatment with TNF blocking agents can be successful, especially if the treatment is indicated for high disease activity of SpA. Adalimumab and infliximab seem to be more effective in lowering the recurrence rate of uveitis compared to etanercept. Psoriasis Psoriasis is a common skin disease with plaque lesions and nail deformities and is primarily treated by the dermatologist. Psoriatic arthritis occurs in 5-20% of the people with psoriasis and can present as a symmetrical polyarthritis, resembling rheumatoid arthritis, but with additional involvement of the DIP-joints (14). Axial disease occurs in about 5% of the psoriasis patients with asymmetrical sacroiliitis in one-third of the cases and spondylitis without sacroiliitis in the rest. Enthesitis and dactylitis are common, especially in the oligoarticular form of the disease. In SpA, patients with psoriatic arthritis excluded, psoriasis occurs in approximately 5-10%. In case of scaling skin lesions or nail changes suspicious for psoriasis in SpA it is recommended to refer the patients to a dermatologist. Skin manifestations of psoriasis usually respond very well to local corticosteroids or PUVA therapy. 3©2007-2014 EULAR
  • 4. Management of spondyloarthritides – Module 7 In case of psoriatic arthritis, NSAID’s and intra-articular injections with corticosteroid are effective in mono-or oligoarthritis (15). Methotrexate is proven to be effective in daily clinical practice for treating the skin and oligo- and polyarthritis, despite the lack of randomized controlled trails to support this (15, 30).). Leflunomide is also effective in both psoriasis and peripheral arthritis, but not on the axial manifestations of SpA (16). TNF alfa blockers, such as infliximab, etanercept, adalimumab, certolizumab and golimumab are efficacious on the skin and nail lesions of psoriasis (15). In some cases treatment of SpA with TNF blocking agents can result in a new manifestations of psoriasis, such as palmoplantarpustulosis (17). Inflammatory Bowel Disease Inflammatory Bowel disease includes Crohn’s disease and ulcerative colitis and is primarily treated by the gastro-enterologist. Approximately 10% of the IBD patients develop SpA. On the other hand, the chance of SpA patients to develop IBD is 5-10%. Asymptomatic inflammatory bowel disease is described in a high percentage of SpA patients (60%) and can be detected by endoscopy of the colon and terminal ileum (18). During follow up studies it appeared that up to 20% of the SpA patients with chronic gut inflammation eventually develop Crohn’s disease (19). Another indication that diseases as SpA and IBD show some overlap is a study on serological markers of IBD. In this study, a high percentage (55%) of AS patients without abdominal complaints had a positive tests for pANCA, ANCA or Omp-C ASCA antibodies (20). In case of persistent or frequently recurring diarrhoea and/or blood or mucus production with the stools it is advised to refer the SpA patients to the gastro-enterologist in order to perform a colonoscopy. Treatment of IBD by the gastro-enterologist is based on immunosuppressive drugs and anti-TNF. The use of NSAID’s can worsen the colitis manifestations, therefore it is advised to minimise the use of these drugs by SpA patients with IBD, except for celecoxib which does not seem to increase the risk at exacerbation of the IBD (21). The use of sulfasalazine can be beneficial for both SpA as well as IBD. The efficacy of other immunosuppressive drugs often used in IBD however, have in most cases not proven efficacy in SpA (22). Of the TNF blocking agents only infliximab and adalimumab are effective in SpA as well as IBD and golimumab is not yet registered for IBD but shows efficacy in ulcerative colitis (23-28). Certolizumab is also effective in IBD but not yet registered in all countries for this indication. Etanercept works well for spinal symptoms in SpA but not on IBD and new manifestations of IBD might even occur during etanercept treatment (28, 29). 4©2007-2014 EULAR
  • 5. Management of spondyloarthritides – Module 7 Therefore, in SpA patients with IBD the use of NSAID’s should be minimised, except for celecoxib, sulfasalazine might show some improvement for both indications and the first choice of anti-TNF is infliximab or adalimumab. Conclusions In SpA physical exercises and NSAID’s are the choice of treatment. In case of peripheral arthritis, sulphasalazine can be added as a useful DMARD. In case of insufficient response at NSAID’s TNF blockers are very effective in SpA, especially infliximab, etanercept, adalimumab, certolizumab and golimumab. These drugs all work very well on the axial manifestations as well as on arthritis, enthesitis and psoriasis. Concerning the treatment of other extra spinal manifestations, anterior uveitis can be treated adequately by the ophthalmologist with local treatment. In refractory uveitis or a high recurrence rate, treatment with adalimumab and infliximab seem to be more effective for this indication compared to etanercept. In case of IBD in SpA, the use of NSAID’s should be minimized but celecoxib can be used if needed. The choice of anti-TNF therapy inSpA with IBD is in favour of infliximab and adalimumab instead of etanercept. Overall, it is important to realize that in SpA extra-articular manifestations do occur frequently and should be taken into account in the choice of treatment, 5©2007-2014 EULAR
  • 6. Management of spondyloarthritides – Module 7 References 1. Linder R, Hoffmann A, Brunner R. Prevalence of the spondyloarthritides in patients with uveitis. J Rheumatol. 2004 Nov;31(11):2226-9. 2. Monnet D, Breban M, Hudry C, Dougados M, Brezin AP. Ophthalmic findings and frequency of extraocular manifestations in patients with HLA-B27 uveitis: a study of 175 cases. Ophthalmology. 2004;111(4):802-9. 3. Pato E, Banares A, Jover JA, Fernandez-Gutierrez B, Godoy F, Morado C, Mendez R, Hernandez-Garcia C. Undiagnosed spondyloarthropathy in patients presenting with anterior uveitis. J Rheumatol. 2000;27(9):2198-202. 4. Linssen A, Rothova A, Valkenburg HA, Dekker-Saeys AJ, et al.The lifetime cumulative incidence of acute anterior uveitis in a normal population and its relation to ankylosing spondylitis and histocompatibility antigen HLA-B27. InvestOphthalmol Vis Sci. 1991;32(9):2568-78. 5. Munoz-Fernandez S, Hidalgo V, Fernandez-Melon J, et al Sulfasalazine reduces the number of flares of acute anterior uveitis over a one-year period. J Rheumatol. 2003 Jun;30(6):1277-9 6. Wakefield D, Chang JH, Amjadi S, Maconochie Z, Abu El-Asrar A, McCluskey P. What is new HLA-B27 acute anterior uveitis? OculImmunolInflamm. 2011Apr;19(2):139-44 7. El-Shabrawi Y, Hermann J. Anti-tumor necrosis factor-alpha therapy with infliximab as an alternative to corticosteroids in the treatment of human leukocyte antigen B27-associated acute anterior uveitis. Ophthalmology. 2002;109(12):2342-6. 8. 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. 9. Foster CS, Tufail F, Waheed NK, Chu D, Miserocchi E, Baltatzis S, Vredeveld CM. Efficacy of etanercept in preventing relapse of uveitis controlled by methotrexate. Arch Ophthalmol. 2003;121(4):437-40. 10. Rosenbaum JT. Effect of etanercept on iritis in patients with ankylosing spondylitis. Arthritis Rheum. 2004;50(11):3736-7. 11. Sieper J, Koenig A, Baumgartner S, Wishneski C, Foehl J, Vlahos B, Freundlich B. Analysis of uveitis rates across all etanerceptankylosing spondylitis clinical trials. Ann Rheum Dis. 2010 Jan;69(1):226- 12. Rudwaleit M, Rødevand E, Holck P, Vanhoof J, Kron M, Kary S, Kupper H. Adalimumab effectively reduces the rate of anterior uveitis flares in patients with active ankylosing spondylitis: results of a prospective open-label study. Ann Rheum Dis. 2009 May;68(5):696-701. 13. van der Horst-Bruinsma IE, van Denderen JC, Visman I, SuttorpSchulten MSA, Dijkmans BAC, Nurmohamed MT. Decreased recurrence rate of uveitis in ankylosing spondylitis treated with adalimumab-an interim analysis. ClinExp Rheumatology 2010;28:630 14. Khan MA. Clinical features of ankylosing spondylitis. In : Rheumatology. Eds Hochberg MC, Silman AJ, Weinblatt ME Weisman MH. Mosby, Edinburg. 2003, vol 2.1161-1181 6©2007-2014 EULAR
  • 7. Management of spondyloarthritides – Module 7 15. Gossec L, Smolen JS, Gaujoux-Viala C, Ash Z, Marzo-Ortega H, van der Heijde D, FitzGerald O, Aletaha D, Balint P, Boumpas D, Braun J, Breedveld FC, Burmester G, Cañete JD, de Wit M, Dagfinrud H, de Vlam K, DougadosM, Helliwell P, Kavanaugh A, Kvien TK, Landewé R, Luger T, Maccarone M, McGonagle D, McHugh N, McInnes IB, Ritchlin C, Sieper J, Tak PP, Valesini G, Vencovsky J, Winthrop KL, Zink A, Emery P; European League Against Rheumatism. European League Against Rheumatism recommendations for the management of psoriatic arthritis with pharmacological therapies. Ann Rheum Dis. 2012 Jan;71(1):4-12. 16. Nash P, Thaçi D, Behrens F, Falk F, Kaltwasser JP. Leflunomide improves psoriasis in patients with psoriatic arthritis: an in-depth analysis of data from the TOPAS study. Dermatology. 2006;212(3):238-49 17. Kary S, Worm M, Audring H, Huscher D, Renelt M, Sorensen H, Stander E, Maass U, Lee H, Sterry W, Burmester GR. New onset or exacerbation of psoriatic skin lesions in patients with definite rheumatoid arthritis receiving tumour necrosis factor alpha antagonists.Ann Rheum Dis. 2006 Mar;65(3):405-7. 18. Mielants H, Veys EM, Cuvelier C, De Vos M. Ileocolonoscopy and spondarthritis.Br J Rheumatol. 1988;27(2):163-4. 19. Mielants H, Veys EM, Goemaere S, Goethals K, Cuvelier C, De Vos M. Gut inflammation in the spondyloarthropathies: clinical, radiologic, biologic, and genetic features in relation to the type of histology. A prospective study. J Rheumatol. 1991;18(10):1542-51 20. deVries M, van der Horst-Bruinsma I, van Hoogstraten I, van Bodegraven A, von Blomberg BM, Ratnawati H, Dijkmans B. pANCA, ASCA, and OmpC antibodies in patients with ankylosing spondylitis without inflammatory bowel disease. J Rheumatol. 2010 Nov;37(11):2340-4. 21. Sandborn WJ, Stenson WF, Brynskov J, Lorenz RG, Steidle GM, Robbins JL, Kent JD, Bloom BJ. Safety of celecoxib in patients with ulcerative colitis in remission: a randomized, placebo-controlled, pilot study. ClinGastroenterolHepatol. 2006 Feb;4(2):203-11 22. Horst-Bruinsma IE van der, Clegg DO, Dijkmans BAC. Treatment of ankylosing spondylitis with disease modifying antirheumatic drugs. ClinExp Rheumatology 2002;20:S67-S70. 23. Braun J, Baraliakos X, Listing J, Davis J, van der Heijde D, Haibel H, Rudwaleit M, Sieper J. Differences in the incidence of flares or new onset of inflammatory bowel diseases in patients with ankylosing spondylitis exposed to therapy with anti-tumor necrosis factor alpha agents.Arthritis Rheum. 2007 May 15;57(4):639-47. 24. Hanauer SB, Feagan BG, Lichtenstein GR, Mayer LF, Schreiber S, Colombel JF, Rachmilewitz D, Wolf DC, Olson A, Bao W, Rutgeerts P; ACCENT I Study Group. Maintenance infliximab for Crohn's disease: the ACCENT I randomised trial. Lancet. 2002 May 4;359(9317):1541-9. 25. Rutgeerts P, Sandborn WJ, Feagan BG, Reinisch W, Olson A, Johanns J, Travers S, Rachmilewitz D, Hanauer SB, Lichtenstein GR, de Villiers WJ, Present D, Sands BE, Colombel JF. Infliximab for induction and maintenance therapy for ulcerative colitis. N Engl J Med. 2005 Dec 8;353(23):2462-76. Erratum in: N Engl J Med. 2006 May 18;354(20):2200. 26. Sandborn WJ, Rutgeerts P, Enns R, Hanauer SB, Colombel JF, Panaccione R, D'Haens G, Li J, Rosenfeld MR, Kent JD, Pollack PF. Adalimumab induction therapy for Crohn disease previously treated with infliximab: a randomized trial. Ann Intern Med. 2007 Jun 19;146(12):829-38. 7©2007-2014 EULAR
  • 8. Management of spondyloarthritides – Module 7 27. Sandborn WJ, Hanauer SB, Rutgeerts P, Fedorak RN, Lukas M, MacIntosh DG, Panaccione R, Wolf D, Kent JD, Bittle B, Li J, Pollack PF. Adalimumab for maintenance treatment of Crohn's disease: results of the CLASSIC II trial. Gut. 2007 Sep;56(9):1232-9. 28. Sandborn WJ, Hanauer SB, Katz S, Safdi M, Wolf DG, Baerg RD, Tremaine WJ, Johnson T, Diehl NN, Zinsmeister AR. Etanercept for active Crohn's disease: a randomized, double-blind, placebo-controlled trial. Gastroenterology. 2001 Nov;121(5):1088-94. 29. Song IH, Appel H, Haibel H, Loddenkemper C, Braun J, Sieper J, Rudwaleit M. New onset of Crohn’s disease during treatment of active ankylosing spondylitis with etanercept. J Rheumatol. 2008 Mar;35(3):532-6. Epub 2008 Jan 15. Erratum in: J Rheumatol. 2008 Apr;35(4):729 30. Carron P, Van Praet L, Jacques P, Elewaut D, Van den Bosch F. Therapy for spondyloarthritis: the role of extra-articular manifestations (eye, skin). Rheum Dis Clin North Am. 2012 Aug;38(3):583-600 8©2007-2014 EULAR