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Effects of tapering tumor necrosis factor inhibitor on the achievement of inactive disease in patients with axial spondyloarthritis: a nationwide cohort study

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dc.contributor.authorPark, JW-
dc.contributor.authorKim, HA-
dc.contributor.authorShin, K-
dc.contributor.authorPark, YB-
dc.contributor.authorKim, TH-
dc.contributor.authorSong, YW-
dc.contributor.authorLee, EY-
dc.date.accessioned2022-01-14T05:18:14Z-
dc.date.available2022-01-14T05:18:14Z-
dc.date.issued2019-
dc.identifier.issn1478-6354-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/20054-
dc.description.abstractOBJECTIVES: To investigate the association between the extent of tapering tumor necrosis factor inhibitor (TNFi) and the likelihood of achieving inactive disease in patients with axial spondyloarthritis (axSpA)
METHODS: We analyzed 1575 1-year follow-up interval data of 776 axSpA patients treated with TNFi for more than 1 year in a nationwide observational cohort. The decision on tapering TNFi was made by patients and their physicians. We quantified TNFi used during interval as a dose quotient (DQ). The intervals were classified into the heavy-tapering (DQ < 50), mild-tapering (DQ 50-99), and control groups (DQ = 100). Outcome variables included achieving Ankylosing Spondylitis Disease Activity Score-inactive disease (ASDAS-ID) and major clinical response of Bath Ankylosing Spondylitis Disease Activity Index (BASDAI50) in the follow-up visit. The effects of TNFi tapering on the outcome were analyzed using the generalized estimating equation.
RESULTS: At the baseline visit, 91.1% of the patients showed a high disease activity (ASDAS-CRP >/= 2.1). DQ of each interval was significantly influenced by the ASDAS-CRP measure in the prior follow-up (P < 0.001). ASDAS-ID was observed in 42.3% of the intervals. A multivariable analysis showed that the likelihood of outcome achievement was comparable between the control and mild-tapering groups, but significantly decreased in the heavy-tapering group (vs. the control group, adjusted OR = 0.28, [95% CI, 0.08-0.94]). In contrast, the likelihood to achieve BASDAI50 response was not different among the groups. In the subgroup of patients who reached ASDAS-ID 1 year after TNFi treatment (n = 327), ASDAS-ID was observed in 66.1% of the subsequent intervals, and only the mild-tapering group showed a likelihood of target maintenance comparable with that of the control group (adjusted OR = 1.25 [0.41-3.80]). This likelihood decreased with an increase in ASDAS-CRP.
CONCLUSION: Mild tapering of TNFi has efficacy comparable with that of the standard-dose treatment for ASDAS-ID achievement in patients with axSpA.
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dc.subject.MESHAdalimumab-
dc.subject.MESHAdult-
dc.subject.MESHAntibodies, Monoclonal-
dc.subject.MESHAntirheumatic Agents-
dc.subject.MESHCohort Studies-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHEtanercept-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHInfliximab-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHSeverity of Illness Index-
dc.subject.MESHSpondylitis, Ankylosing-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHTumor Necrosis Factor Inhibitors-
dc.subject.MESHTumor Necrosis Factor-alpha-
dc.titleEffects of tapering tumor necrosis factor inhibitor on the achievement of inactive disease in patients with axial spondyloarthritis: a nationwide cohort study-
dc.typeArticle-
dc.identifier.pmid31272498-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611048/-
dc.subject.keywordDose tapering-
dc.subject.keywordInactive disease-
dc.subject.keywordSpondyloarthritis-
dc.subject.keywordTumor necrosis factor-
dc.contributor.affiliatedAuthorKim, HA-
dc.type.localJournal Papers-
dc.identifier.doi10.1186/s13075-019-1943-6-
dc.citation.titleArthritis research & therapy-
dc.citation.volume21-
dc.citation.number1-
dc.citation.date2019-
dc.citation.startPage163-
dc.citation.endPage163-
dc.identifier.bibliographicCitationArthritis research & therapy, 21(1). : 163-163, 2019-
dc.identifier.eissn1478-6362-
dc.relation.journalidJ014786354-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Rheumatology
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