2020
DOI: 10.1177/1759720x20975912
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Conventional disease-modifying antirheumatic drugs therapy may not slow spinal radiographic progression in ankylosing spondylitis: results from an 18-year longitudinal dataset

Abstract: Objectives: The clinical benefit of conventional disease-modifying antirheumatic drugs (cDMARDs) for treating ankylosing spondylitis (AS) is generally limited to improvements in peripheral arthritis. However, cDMARDs could be conditionally considered as alternatives to established drugs for improving axial manifestations in exceptional circumstances. However, there are few studies of the impact of cDMARDs on radiographic progression outcomes. Therefore, we investigated the effectiveness of cDMARDs on radiograp… Show more

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Cited by 17 publications
(20 citation statements)
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“…This recommendation is unchanged for the axial phenotype. There is no recent data suggestive of an effect on symptoms or potential beneficial structural effect on radiographs [77]. Nevertheless, when used in combination with a TNF inhibitor, methotrexate (MTX) reduces the immunogenicity of the anti-TNF agent and may increase the long-term maintenance of these drugs [78].…”
Section: Conventional Synthetic Disease-modifying Antirheumatic Drugs (Csdmards Such As Methotrexate Leflunomide and Sulfasalazine) Are Nmentioning
confidence: 99%
“…This recommendation is unchanged for the axial phenotype. There is no recent data suggestive of an effect on symptoms or potential beneficial structural effect on radiographs [77]. Nevertheless, when used in combination with a TNF inhibitor, methotrexate (MTX) reduces the immunogenicity of the anti-TNF agent and may increase the long-term maintenance of these drugs [78].…”
Section: Conventional Synthetic Disease-modifying Antirheumatic Drugs (Csdmards Such As Methotrexate Leflunomide and Sulfasalazine) Are Nmentioning
confidence: 99%
“…Longitudinal modified Stoke Ankylosing Spondylitis Spinal Score (mSASSS) data were used to evaluate the difference in radiographic progression between the controlled and uncontrolled CRP groups. According to previous studies, the intraobserver and interobserver reliability values of the mSASSS are excellent (intraclass coefficient: 0.978, 95% confidence interval [CI] 0.976 to 0.979, and 0.946, 95% CI 0.941 to 0.950, respectively) 10,11 …”
Section: Methodsmentioning
confidence: 82%
“…Data of patients who were diagnosed with r‐axSpA according to the modified New York criteria 9 at a single center between January 2001 and December 2018 were extracted from the electronic medical records (EMR) 10,11 . The inclusion criteria were as follows: (1) patients diagnosed with r‐axSpA and under follow‐up; (2) those who had 2 or more radiographs taken; (3) those who were evaluated using the Ankylosing Spondylitis Disease Activity Score and Bath Ankylosing Spondylitis Disease Activity Index (BASDAI); (4) those who underwent blood tests; (and 5) those who had 2 or more visits at the rheumatology clinic.…”
Section: Methodsmentioning
confidence: 99%
“…Fourth, most patients treated with TNFi had high baseline in ammation, and their changes in mSASSS were shown to be different from those who had not been treated with TNFi. 11,24 Therefore, the delayed effect of in ammation on mSASSS may be different in patients not treated with TNFi.…”
Section: Discussionmentioning
confidence: 99%
“…
Objectives: To determine the relationship between in ammation and radiographic progression over time in patients in clinical remission for ankylosing spondylitis (AS) after tumor necrosis factor inhibitor (TNFi) treatment.Method: Medical records data of AS patients with Bath Ankylosing Spondylitis Disease Activity Index scores <4 during TNFi treatment were analysed at 6month intervals from January 2001 to December 2018. To determine the relationship between the modi ed Stoke Ankylosing Spondylitis Spinal Score (mSASSS) and C-reactive protein (CRP) over time, we tted linear mixed models with mSASSS as the response variable, baseline mSASSS and the cumulative sum of CRP with different lag times (6,12, 18,24, 30, and 36 months) as xed effects, and patients as random effects. Associations between mSASSS and the cumulative sum of CRP or the lag times with the highest beta coe cients were further investigated with linear mixed models that included additional clinical variables.Results: A total of 2,956 intervals were obtained from 333 patients.
…”
mentioning
confidence: 99%