Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/42507
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dc.contributor.authorDe Craemer, A. S.-
dc.contributor.authorDe Hooge, M.-
dc.contributor.authorRenson, T.-
dc.contributor.authorDeroo, L.-
dc.contributor.authorVarkas, G.-
dc.contributor.authorVan Praet , L.-
dc.contributor.authorJoos, R.-
dc.contributor.authorLENAERTS , Joke-
dc.contributor.authorDevink, M.-
dc.contributor.authorGyselbrecht, L.-
dc.contributor.authorPeene, I.-
dc.contributor.authorTHEVISSEN, Kristof-
dc.contributor.authorCarron, P.-
dc.contributor.authorVan den Bosch, F.-
dc.contributor.authorElewaut, D.-
dc.date.accessioned2024-03-01T08:00:15Z-
dc.date.available2024-03-01T08:00:15Z-
dc.date.issued2023-
dc.date.submitted2024-03-01T07:15:28Z-
dc.identifier.citationANNALS OF THE RHEUMATIC DISEASES, 82 , p. 617 -618-
dc.identifier.urihttp://hdl.handle.net/1942/42507-
dc.description.abstractBackground: Improvement in functioning and health as assessed by the ASAS Health Index (HI) is an important outcome of interventions in patients with axial spondyloarthritis (axSpA). The ability of various ASAS HI thresholds to discriminate between treatment arms of an active comparator trial have been demonstrated recently by our group with absolute improvement in the ASAS HI in general being superior to relative changes [1, 2]. Objectives: To assess whether ASAS HI response measures (absolute improvement of ≥3.0 and relative improvement of ≥30%) and reaching a status of good global functioning (ASAS HI ≤5.0) adequately discriminate between the changes and states in relevant external outcomes. Methods: In this post-hoc analysis from the tight-controlled, treat-to-target (T2T) trial TICOSPA (2), data of active axSpA patients randomized to either the T2T arm (visits every 4 weeks, prespecified strategy of treatment intensification until achieving low disease activity) or usual care (UC; visits every 12 weeks, treatment at the rheumatologist's discretion) were used. The performance of ASAS HI response-and status scores against change (ASAS-40/ BASDAI-50 response, change in patient global/ BASDAI, and ASDAS improvement) and external status scores (ASAS partial remission, ASDAS status) was assessed, respectively. Analysis were performed by comparing the mean values and proportion of responses of continuous and dichotomous response outcomes, by t-tests. Missing data on outcomes was handled by non-responder imputation (NRI). Results: ASAS HI was available in 160 patients, both at baseline and at week 48. At w48, an ASAS HI improvement of ≥30%, improvement of ≥3 points and ASAS HI ≤5.0 was achieved by 56 (35%), 51 (31.9%) and 54 (33.7%) patients, respectively. Patients with a meaningful improvement in global functioning had a larger reduction in patient global and disease activity as well a greater chance to reach remission compared to patients with no significant improvement in global functioning (Table 1). Health outcomes were not different between the two response measures of ASAS HI. Patients who achieved ASAS partial remission, ASDAS inactive disease or ASDAS low activity at week 48 were more likely to have an ASAS HI ≤ 5.0 compared with patients who did not achieve such states (Figure 1). Conclusion: We demonstrated discriminant capacity of both, the relative and the absolute response measures of the ASAS HI. Both thresholds proved to have external validity and were able to discriminate between active treatment arms. REFERENCES: [1] EULAR 2022, [2] Molto A et al. Ann Rheum Dis 2021 Figure 1. Proportion of patients reaching status of good global functioning at week 48 Table 1. Comparison of clinical outcomes and ASAS HI response at follow up ASAS HI response = > 30% improvement (NRI) ASAS HI response = > 3 points improvement (NRI) Yes (n=56) No (n=104) p YES (n=51) No (n=109) p ASAS40 response at w48 48.2% 21.2% <0.00151.0% (21.1% <0.001 BASDAI 50 at w48 71.4% 28.8% <0.00168.6% 32.1% <0.001 ASDAS Major improvement (0 to 48w) 23.2% 6.7% 0.005 23.5% 7.3% 0.008 ASDAS Clinically Important Improvement (0 to 48w) 62.5% 24.0% <0.00160.8% 26.6% <0.001 Change in Patient Global (0 to 48w) Mean (Missing 0 (0%) 18 (17.3%) 0 (0%) 18 (16.5%) Change in BASDAI (0 to 48w) Mean (SD)-2.79 (2.09)-1.42 (2.04) <0.001-2.95 (2.17)-1.40 (1.96) <0.001 Median [Min. Max]-2.60 [-8.90. 1.40]-1.25 [-8.60. 3.00]-3.00 [-8.90. 1.40]-1.20 [-8.60. 3.00] Missing 0 (0%) 18 (17.3%) 0 (0%) 18 (16.5%)-
dc.language.isoen-
dc.publisherBMJ PUBLISHING GROUP-
dc.subject.otherImaging-
dc.titleRheumatologists overcall sacroiliitis on X-ray and MRI in axial spondyloarthritis patients: Data from the Belgian inflammatory arthritis and spondylitis cohort (Be-Giant)-
dc.typeJournal Contribution-
local.bibliographicCitation.conferencedateMAY 31-JUN 03, 2023-
local.bibliographicCitation.conferencenameEuropean Congress of Rheumatology (EULAR)-
local.bibliographicCitation.conferenceplaceMilan, ITALY-
dc.identifier.epage618-
dc.identifier.spage617-
dc.identifier.volume82-
local.format.pages2-
local.bibliographicCitation.jcatM-
local.publisher.placeBRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedMeeting Abstract-
dc.identifier.doi10.1136/annrheumdis-2023-eular.2231-
dc.identifier.isi001107398702068-
local.provider.typewosris-
local.description.affiliation[De Craemer, A. S.; De Hooge, M.; Renson, T.; Deroo, L.; Varkas, G.; Joos, R.; Peene, I.; Carron, P.; Van den Bosch, F.; Elewaut, D.] Ghent Univ Hosp, Rheumatol, Ghent, Belgium.-
local.description.affiliation[De Craemer, A. S.; De Hooge, M.; Renson, T.; Deroo, L.; Varkas, G.; Carron, P.; Van den Bosch, F.; Elewaut, D.] Univ Ghent, Internal Med & Pediat, Fac Med & Hlth Sci, Ghent, Belgium.-
local.description.affiliation[De Craemer, A. S.; De Hooge, M.; Renson, T.; Deroo, L.; Varkas, G.; Carron, P.; Van den Bosch, F.; Elewaut, D.] VIB UGent, Ctr Inflammat Res, Ghent, Belgium.-
local.description.affiliation[Van Praet, L.] AZ Maria Middelares, Rheumatol, Ghent, Belgium.-
local.description.affiliation[Joos, R.] ZNA Jan Palfijn, Rheumatol, Merksem, Belgium.-
local.description.affiliation[Lenaerts, J.] Reuma Inst, Rheumatol, Hasselt, Belgium.-
local.description.affiliation[Lenaerts, J.] AZ Jessa Hosp, Rheumatol, Hasselt, Belgium.-
local.description.affiliation[Devink, M.] AZ Sint Lucas, Rheumatol, Brugge, Belgium.-
local.description.affiliation[Gyselbrecht, L.] Algemeen Stedelijk Ziekenhuis, Rheumatol, Aalst, Belgium.-
local.description.affiliation[Peene, I.] Acad Hosp St Jan, Rheumatol, Brugge, Belgium.-
local.description.affiliation[Thevissen, K.] Reumactr, Rheumatol, Genk, Belgium.-
local.description.affiliation[Thevissen, K.] Ziekenhuis Oost Limburg, Rheumatol, Genk, Belgium.-
local.description.affiliation[Carron, P.] AZ Alma, Rheumatol, Eeklo Sijsele, Belgium.-
local.uhasselt.internationalno-
item.fullcitationDe Craemer, A. S.; De Hooge, M.; Renson, T.; Deroo, L.; Varkas, G.; Van Praet , L.; Joos, R.; LENAERTS , Joke; Devink, M.; Gyselbrecht, L.; Peene, I.; THEVISSEN, Kristof; Carron, P.; Van den Bosch, F. & Elewaut, D. (2023) Rheumatologists overcall sacroiliitis on X-ray and MRI in axial spondyloarthritis patients: Data from the Belgian inflammatory arthritis and spondylitis cohort (Be-Giant). In: ANNALS OF THE RHEUMATIC DISEASES, 82 , p. 617 -618.-
item.fulltextWith Fulltext-
item.contributorDe Craemer, A. S.-
item.contributorDe Hooge, M.-
item.contributorRenson, T.-
item.contributorDeroo, L.-
item.contributorVarkas, G.-
item.contributorVan Praet , L.-
item.contributorJoos, R.-
item.contributorLENAERTS , Joke-
item.contributorDevink, M.-
item.contributorGyselbrecht, L.-
item.contributorPeene, I.-
item.contributorTHEVISSEN, Kristof-
item.contributorCarron, P.-
item.contributorVan den Bosch, F.-
item.contributorElewaut, D.-
item.accessRightsOpen Access-
crisitem.journal.issn0003-4967-
crisitem.journal.eissn1468-2060-
Appears in Collections:Research publications
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