The contribution of joint and skin improvements to the health-related quality of life of patients with psoriatic arthritis: a post hoc analysis of two randomised controlled studies
- PMID: 31113794
- PMCID: PMC6788877
- DOI: 10.1136/annrheumdis-2018-215003
The contribution of joint and skin improvements to the health-related quality of life of patients with psoriatic arthritis: a post hoc analysis of two randomised controlled studies
Abstract
Objective: Determine the contribution of joint and skin improvements to health-related quality of life (HRQoL) in patients with psoriatic arthritis (PsA).
Methods: SPIRIT-P1 and SPIRIT-P2 are phase 3 trials investigating ixekizumab, an interleukin-17A antagonist, in the treatment of patients with active PsA. Patients were randomised to ixekizumab or placebo. Outcomes included the Disease Activity Index for Psoriatic Arthritis (DAPSA), the Psoriasis Area and Severity Index (PASI), the European Quality of Life-Five Dimensions (EQ-5D) Visual Analogue Score (VAS), the 36-Item Short-Form Health Survey (SF-36) and the Work Productivity and Activity Impairment (WPAI) Questionnaire. The contribution of joint and skin improvements to HRQoL was modelled using a smoothing spline method and depicted with response surface graphics.
Results: In this integrated analysis, 402 patients with PsA had baseline psoriasis of ≥3% of body surface area. We applied response surface modelling to this patient data set to investigate the relationship between DAPSA, PASI and HRQoL improvements at week 24. The greatest improvement in EQ-5D VAS was associated with the largest per cent improvements in both DAPSA and PASI together, rather than DAPSA or PASI alone. Similar observations were made in domains of SF-36 and WPAI.
Conclusion: Optimal improvements in patients' HRQoL were dependent on successful treatment of both joint and skin symptoms.
Keywords: health-related quality of life; psoriasis; psoriatic arthritis; treatment.
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Conflict of interest statement
Competing interests: AK has been a consultant for Eli Lilly and Company. AG has received consulting or advisory board honoraria, speaking honoraria and/or grants from Abbvie, BMS, Celgene Corporation, Dermira, Eli Lilly and Company, Incyte Corporation, Janssen Biotech, Janssen-Ortho, LEO Pharma, US, Lilly ICOS LLC, Novartis, Sun Pharmaceuticals and UCB. AM has received grant support and lecture fees from AbbVie, Esai, Kyowa Hakko Kirin, Leo Pharma, Maruho, Mitsubishi Tanabe Pharma, Novartis and Torii Pharmaceutical and lecture fees from Celgene, Eli Lilly Japan and Janssen Pharmaceutical. JFM has received consulting fees, speaking fees and/or honoraria from AbbVie, Eli Lilly, Novartis, Pfizer, UCB, Celgene, Sanofi, Regeneron, Merck, Biogen Idec and Janssen, and has served as a paid consultant for investment analysis companies Cowen Group and GLG. CYL, JB and MMH are full-time employees and shareholders of Eli Lilly and Company. CLS is a former employee and shareholder of Eli Lilly and Company. DT has been a consultant and advisor and has received speaking fees and grants, and served as an investigator in clinical trials for the following companies: AbbVie, Almirall, Amgen, Biogen Idec, BMS, Boehringer Ingelheim, Celgene, Dignity, Dermavant, Eli Lilly, Galapagos, GSK, Galderma, LEO Pharma, Janssen-Cilag, MSD, Novartis, Pfizer and Regeneron.
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References
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- Sokoll KB, Helliwell PS. Comparison of disability and quality of life in rheumatoid and psoriatic arthritis. J Rheumatol 2001;28:1842–6. - PubMed
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