TY - JOUR
T1 - Predictors of ASDAS-CRP inactive disease in axial spondyloarthritis during treatment with TNF-inhibitors
T2 - Data from the EuroSpA collaboration
AU - Ørnbjerg, Lykke M.
AU - Linde, Louise
AU - Georgiadis, Stylianos
AU - Rasmussen, Simon H.
AU - Lindström, Ulf
AU - Askling, Johan
AU - Michelsen, Brigitte
AU - Giuseppe, Daniela Di
AU - Wallman, Johan K.
AU - Pavelka, Karel
AU - Závada, Jakub
AU - Nissen, Michael J.
AU - Jones, Gareth T.
AU - Relas, Heikki
AU - Pirilä, Laura
AU - Tomšič, Matija
AU - Rotar, Ziga
AU - Geirsson, Arni Jon
AU - Gudbjornsson, Bjorn
AU - Kristianslund, Eirik K.
AU - van sder Horst-Bruinsma, Irene
AU - Loft, Anne Gitte
AU - Laas, Karin
AU - Iannone, Florenzo
AU - Corrado, Addolorata
AU - Ciurea, Adrian
AU - Santos, Maria J.
AU - Santos, Helena
AU - Codreanu, Catalin
AU - Akkoc, Nurullah
AU - Gunduz, Ozgul S.
AU - Glintborg, Bente
AU - Østergaard, Mikkel
AU - Hetland, Merete Lund
N1 - Funding Information
This work was supported by Novartis Pharma AG .
Acknowledgments
The EuroSpA Research Collaboration Network was financially supported by Novartis Pharma AG. Novartis had no influence on the data collection, statistical analyses, manuscript preparation or decision to submit the manuscript. Professor Gary Macfarlane (University of Aberdeen) is Chief Investigator of BSRBR-AS and facilitated access to the UK data used in this study.
Corrigendum to ‘Predictors of ASDAS-CRP inactive disease in axial spondyloarthritis during treatment with TNF-inhibitors: data from the EuroSpA collaboration’ [Seminars in Arthritis and Rheumatism 56 (2022) 1-13/152081]
https://doi.org/10.1016/j.semarthrit.2022.152141
PY - 2022/10/1
Y1 - 2022/10/1
N2 - 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.
AB - 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.
KW - Ankylosing spondylitis disease activity score
KW - Axial spondyloarthritis
KW - Predictors
KW - TNF-inhibitors
UR - http://www.scopus.com/inward/record.url?scp=85135923596&partnerID=8YFLogxK
U2 - 10.1016/j.semarthrit.2022.152081
DO - 10.1016/j.semarthrit.2022.152081
M3 - Article
C2 - 35985172
AN - SCOPUS:85135923596
VL - 56
JO - Seminars in arthritis and rheumatism
JF - Seminars in arthritis and rheumatism
SN - 0049-0172
M1 - 152081
ER -