Predictors of ASDAS-CRP inactive disease in axial spondyloarthritis during treatment with TNF-inhibitors : Data from the EuroSpA collaboration
| dc.contributor.author | Ørnbjerg, Lykke Midtbøll | |
| dc.contributor.author | Linde, Louise | |
| dc.contributor.author | Georgiadis, Stylianos | |
| dc.contributor.author | Horskjær Rasmussen, Simon | |
| dc.contributor.author | Lindström, Ulf | |
| dc.contributor.author | Askling, Johan | |
| dc.contributor.author | Michelsen, Brigitte | |
| dc.contributor.author | Di Giuseppe, Daniela | |
| dc.contributor.author | Wallman, Johan K. | |
| dc.contributor.author | Pavelka, Karel | |
| dc.contributor.author | Závada, Jakub | |
| dc.contributor.author | Nissen, Michael J | |
| dc.contributor.author | Jones, Gareth T. | |
| dc.contributor.author | Relas, Heikki | |
| dc.contributor.author | Pirilä, Laura | |
| dc.contributor.author | Tomšič, Matija | |
| dc.contributor.author | Rotar, Ziga | |
| dc.contributor.author | Geirsson, Árni Jón | |
| dc.contributor.author | Guðbjörnsson, Björn | |
| dc.contributor.author | Kristianslund, Eirik K. | |
| dc.contributor.author | van sder Horst-Bruinsma, Irene | |
| dc.contributor.author | Loft, Anne Gitte | |
| dc.contributor.author | Laas, Karin | |
| dc.contributor.author | Iannone, Florenzo | |
| dc.contributor.author | Corrado, Addolorata | |
| dc.contributor.author | Ciurea, Adrian | |
| dc.contributor.author | Santos, Maria José | |
| dc.contributor.author | Santos, Helena | |
| dc.contributor.author | Codreanu, Catalin | |
| dc.contributor.author | Akkoc, Nurullah | |
| dc.contributor.author | Gunduz, Ozgul S. | |
| dc.contributor.author | Glintborg, Bente | |
| dc.contributor.author | Østergaard, Mikkel | |
| dc.contributor.author | Lund Hetland, Merete | |
| dc.contributor.department | Faculty of Medicine | |
| dc.date.accessioned | 2025-11-20T08:50:55Z | |
| dc.date.available | 2025-11-20T08:50:55Z | |
| dc.date.issued | 2022-10-01 | |
| dc.description | Funding Information: LMØ, LL, SG and SHR: research grants from Novartis; UL: none; DDG none; JKW: consultant of AbbVie, Amgen, Celgene, Eli Lilly and Novartis; BG: research grants from Pfizer, Abbvie and BMS; LP: consultant of Novartis Finland, UCB Pharma, Pfizer, Sanofi, BMS, AbbVie, Amgen, Celgene, Eli Lilly, Boehringer-Ingelheim, Mylan; KL: consulting and/or speaking fees from Amgen, Johnson and Johnson and Novartis; ACo: research grants, consulting and/or speaking fees from Amgen, Lilly, Pfizer, Boehringer Ingelheim; KP: speaker and consulting fees from Pfizer, MSD, BMS, UCB, Amgen, Egis, Roche, AbbVie; JZ: speaker and consulting fees from Abbvie, Elli-Lilly, Sandoz, Novartis, Egis, UCB; EKK: none; NA: speaking fees from Pfizer; ÖSG: none; HS: research grant from Sociedade Portuguesa de Reumatologia and speaker and/or consultancy fees from Abbvie, Janssen, Lilly, Novartis and Pfizer; MJN: consulting and/or speaking fees from AbbVie, Eli Lilly, Janssens, Novartis and Pfizer; BM: research grant from Novartis; GTJ: research grants from AbbVie, Pfizer, UCB, Amgen, GSK. Speaker fee from Janssen; HR: consulting and/or speaking fees from Abbvie, Celgene, Pfizer, UCB, and Viatris; MT: consulting and/or speaking fees from Abbvie, Amgen, Biogen, Eli Lilly, Janssen, Medis, MSD, Novartis, Pfizer, Sanofi, Sandoz-Lek; AJG: none; IHB: Consultant for Abbvie, UCB, MSD, Novartis, Lilly, unrestricted Grants received for investigator initiated studies from: MSD, Pfizer, AbbVie, UCB, fees received for Lectures from BMS, AbbVie, Pfizer, MSD ; JA: PI for agreements between Karolinska Institutet and Abbvie, Astra-Zeneca, BMS, Eli Lilly, Janssen, MSD, Pfizer, Roche, Samsung Bioepis, Sanofi, and UCB; FI: consulting and/or speaking from Abbvie, Amgen, AstraZeneca, BMS, Galapagos, Janssen, Lilly, MSD, Novartis, Pfizer, Roche and UCB; AGL: Research Grant from Novartis, and speaker and/or consultancy fees from AbbVie, Janssen, Lilly, MSD, Novartis, Pfizer, Roche, and UCB; ACi: consulting and/or speaking fees from AbbVie, Eli Lilly, Merck Sharp & Dohme, Novartis and Pfizer; MJS: speaker fees from Abbvie, AstraZeneca, Lilly, Novartis and Pfizer; CC: Speaker and consultancy fees from AbbVie, Amgen, Boehringer Ingelheim, Ewopharma, Lilly, Novartis, Pfizer; ZR: speaker or consultancy fees from Abbvie, Novartis, MSD, Medis, Biogen, Eli Lilly, Pfizer, Sanofi, Lek, Janssen; BjG: consulting and/or speaking fees from Amgen and Novartis; MØ: research grants from Abbvie, BMS, Merck, Celgene and Novartis, and speaker and/or consultancy fees from Abbvie, BMS, Boehringer-Ingelheim, Celgene, Eli-Lilly, Hospira, Janssen, Merck, Novartis, Novo, Orion, Pfizer, Regeneron, Roche, Sandoz, Sanofi and UCB; MLH: Research grants from Abbvie, Biogen, BMS, Celltrion, Eli Lilly, Janssen Biologics B.V, Lundbeck Fonden, MSD, Medac, Pfizer, Roche, Samsung Biopies, Sandoz, Novartis. Funding Information: This work was supported by Novartis Pharma AG . Publisher Copyright: © 2022 Copyright © 2022. Published by Elsevier Inc. | en |
| dc.description.abstract | Objectives: In patients with axial spondyloarthritis (axSpA) initiating their first tumor necrosis factor alpha-inhibitor (TNFi), we aimed to identify common baseline predictors of Ankylosing Spondylitis Disease Activity Score (ASDAS-CRP) inactive disease (primary objective) and clinically important improvement (CII) at 6 months, and drug retention at 12-months across 15 European registries. Methods: Baseline demographic and clinical characteristics were collected. Outcomes were investigated per registry and in pooled data using logistic regression analyses on multiply imputed data. Results: The consistency of baseline predictors in individual registries justified pooling the data. In the pooled dataset (n = 21,196), the 6-month rates for ASDAS inactive disease and ASDAS CII were 26% and 51%, and the 12-month drug retention rate 65% in patients with available data (n = 9,845, n = 6,948 and n = 21,196, respectively). Nine common baseline predictors of ASDAS inactive disease, ASDAS CII and 12-month drug retention were identified, and the odds ratios (95%-confidence interval) for ASDAS inactive disease were: age, per year: 0.97 (0.97–0.98), men vs. women: 1.88 (1.60–2.22), current vs. non-smoking: 0.76 (0.63–0.91), HLA-B27 positive vs. negative: 1.51 (1.20–1.91), TNF start year 2015–2018 vs. 2009–2014: 1.24 (1.06–1.45), CRP>10 vs. ≤10 mg/l: 1.49 (1.25–1.77), one unit increase in health assessment questionnaire (HAQ): 0.77 (0.58–1.03), one-millimeter (mm) increase in Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) fatigue and spinal pain: 0.99 (0.99–1.00) and 0.99 (0.99–1.99), respectively Conclusion: Common baseline predictors of treatment response and adherence to TNFi could be identified across data from 15 European registries, indicating that they may be universal across different axSpA populations. | en |
| dc.description.version | Peer reviewed | en |
| dc.format.extent | 1393551 | |
| dc.format.extent | 152081 | |
| dc.identifier.citation | Ørnbjerg, L M, Linde, L, Georgiadis, S, Horskjær Rasmussen, S, Lindström, U, Askling, J, Michelsen, B, Di Giuseppe, D, Wallman, J K, Pavelka, K, Závada, J, Nissen, M J, Jones, G T, Relas, H, Pirilä, L, Tomšič, M, Rotar, Z, Geirsson, Á J, Guðbjörnsson, B, Kristianslund, E K, van sder Horst-Bruinsma, I, Loft, A G, Laas, K, Iannone, F, Corrado, A, Ciurea, A, Santos, M J, Santos, H, Codreanu, C, Akkoc, N, Gunduz, O S, Glintborg, B, Østergaard, M & Lund Hetland, M 2022, 'Predictors of ASDAS-CRP inactive disease in axial spondyloarthritis during treatment with TNF-inhibitors : Data from the EuroSpA collaboration', Seminars in Arthritis and Rheumatism, vol. 56, 152081, pp. 152081. https://doi.org/10.1016/j.semarthrit.2022.152081 | en |
| dc.identifier.doi | 10.1016/j.semarthrit.2022.152081 | |
| dc.identifier.issn | 0049-0172 | |
| dc.identifier.other | 62301338 | |
| dc.identifier.other | e1719022-b286-42ea-b10d-42c9dc65af01 | |
| dc.identifier.other | 85135923596 | |
| dc.identifier.other | 35985172 | |
| dc.identifier.other | unpaywall: 10.1016/j.semarthrit.2022.152081 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.11815/6804 | |
| dc.language.iso | en | |
| dc.relation.ispartofseries | Seminars in Arthritis and Rheumatism; 56() | en |
| dc.relation.url | https://www.scopus.com/pages/publications/85135923596 | en |
| dc.rights | info:eu-repo/semantics/openAccess | en |
| dc.subject | Ankylosing spondylitis disease activity score | en |
| dc.subject | Axial spondyloarthritis | en |
| dc.subject | Predictors | en |
| dc.subject | TNF-inhibitors | en |
| dc.subject | Severity of Illness Index | en |
| dc.subject | Spondylarthritis/drug therapy | en |
| dc.subject | Humans | en |
| dc.subject | Male | en |
| dc.subject | Tumor Necrosis Factor Inhibitors/therapeutic use | en |
| dc.subject | Female | en |
| dc.subject | Registries | en |
| dc.subject | Axial Spondyloarthritis | en |
| dc.subject | Spondylitis, Ankylosing/drug therapy | en |
| dc.subject | Anesthesiology and Pain Medicine | en |
| dc.subject | Rheumatology | en |
| dc.title | Predictors of ASDAS-CRP inactive disease in axial spondyloarthritis during treatment with TNF-inhibitors : Data from the EuroSpA collaboration | en |
| dc.type | /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article | en |
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