TY - JOUR
T1 - Evaluation of changes in skin and joint outcomes and associated treatment changes in psoriatic arthritis (PsA)
T2 - Experience from the corrona PsA/SpA registry
AU - Mease, Philip J.
AU - Etzel, Carol J.
AU - Huster, William J.
AU - Armstrong, April W.
AU - Muram, Talia M.
AU - Lisse, Jeffrey
AU - Rebello, Sabrina
AU - Dodge, Rhiannon
AU - Murage, Mwangi J.
AU - Greenberg, Jeffrey D.
AU - Malatestinic, William N.
N1 - Funding Information:
This study was sponsored by Corrona, LLC. Corrona, LLC has been supported through contracted subscriptions in the last 2 years by AbbVie, Amgen, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Crescendo, Eli Lilly and Company, Genentech, Gilead, GSK, Janssen, Momenta Pharmaceuticals, Novartis, Pfizer Inc., Regeneron, Roche, Merck, UCB, and Valeant. 1P.J. Mease, MD, MACR, Swedish-Providence-St. John Health Systems, and University of Washington, Seattle, Washington; 2C.J. Etzel, PhD, S. Rebello, MPH, R. Dodge, MS, Corrona, LLC, Waltham, Massachusetts; 3W. Huster, PhD, T. Muram, MD, J. Lisse, MD, M.J. Murage, PhD, MPH, W. Malatestinic, PharmD, MBA, Eli Lilly and Company, Indianapolis, Indiana; 4A. Armstrong, MD, MPH, University of Southern California, Los Angeles, California; 5J.D. Greenberg, MD, MPH, Corrona, LLC, Waltham, Massachusetts, and New York School of Medicine, New York, New York, USA. PJM has received research grants from Novartis, AbbVie, Amgen, BMS, Janssen, Eli Lilly, Novartis, Pfizer, SUN, and UCB; consultant fees from Abbvie, Amgen, BMS, Celgene, Corrona, Galapagos, Gilead, Janssen, Leo, Eli Lilly, Merck, Novartis, Pfizer, SUN, and UCB; and speakers bureau fees for AbbVie, Amgen, BMS, Genentech, Janssen, Eli Lilly, Novartis, Pfizer, and UCB. AWA has acted as an investigator, advisor and/or consultant to AbbVie, Janssen, Novartis, Eli Lilly, Regeneron, Sanofi, Leo, Science 37, Modernizing Medicine, and Ortho Dermatologics. TMM, JL, WNM, MJM, and WJH are employees of and hold stock in Eli Lilly. RD and SR are employees of Corrona, LLC. CJE is an employee and holds stock in Corrona, LLC, and is on the advisory board to Merck. JDG is an employee and holds stock in Corrona, LLC, and is a consultant for Genentech, Janssen, Novartis, Pfizer, and Eli Lilly. Address correspondence to Dr. P.J. Mease, Seattle Rheumatology Associates, 601 Broadway, Suite 600, Seattle, WA 98122, USA. Email: [email protected]. Accepted for publication March 20, 2020.
Publisher Copyright:
Copyright © 2021 All rights reserved
PY - 2021/3/1
Y1 - 2021/3/1
N2 - Objective. To characterize skin severity and joint activity outcomes and associated treatment changes in patients with psoriatic arthritis (PsA) through 12 months of follow-up after enrollment in the Corrona Psoriatic Arthritis/Spondyloarthritis (PsA/SpA) Registry. Methods. Patients ≥ 18 years of age with a diagnosis of PsA and a history of psoriasis between March 21, 2013, and September 30, 2016, were enrolled (n = 647). Demographics, clinical features, and treatment characteristics were collected and stratified by skin severity and joint activity. Change in joint and skin from enrollment to the 12-month visit was classified by change in category of Clinical Disease Activity Index (CDAI) or body surface area (BSA). Tests of association evaluated the relationship between changes in therapy and changes in skin severity and joint activity. Results. Patients with improvement in both joint activity and skin severity saw the largest median reduction in both CDAI and BSA, while those who worsened in both had the greatest median increase in both CDAI and BSA. The majority of PsA patients (> 50%) had no change in skin severity regardless if they had reduced therapy (50%), no therapy changes (54%), or increased therapy (56%; P = 0.5875). However, there was a significant association between changes in therapy and changes in joint activity (P < 0.001). Patients who increased therapy were more likely to have improvement in joint activity (32%) compared to patients who reduced therapy (22%) or had no therapy changes (11%). Conclusion. The clinical implication for our findings suggests the assessment and incorporation of both skin and joint components may be advisable.
AB - Objective. To characterize skin severity and joint activity outcomes and associated treatment changes in patients with psoriatic arthritis (PsA) through 12 months of follow-up after enrollment in the Corrona Psoriatic Arthritis/Spondyloarthritis (PsA/SpA) Registry. Methods. Patients ≥ 18 years of age with a diagnosis of PsA and a history of psoriasis between March 21, 2013, and September 30, 2016, were enrolled (n = 647). Demographics, clinical features, and treatment characteristics were collected and stratified by skin severity and joint activity. Change in joint and skin from enrollment to the 12-month visit was classified by change in category of Clinical Disease Activity Index (CDAI) or body surface area (BSA). Tests of association evaluated the relationship between changes in therapy and changes in skin severity and joint activity. Results. Patients with improvement in both joint activity and skin severity saw the largest median reduction in both CDAI and BSA, while those who worsened in both had the greatest median increase in both CDAI and BSA. The majority of PsA patients (> 50%) had no change in skin severity regardless if they had reduced therapy (50%), no therapy changes (54%), or increased therapy (56%; P = 0.5875). However, there was a significant association between changes in therapy and changes in joint activity (P < 0.001). Patients who increased therapy were more likely to have improvement in joint activity (32%) compared to patients who reduced therapy (22%) or had no therapy changes (11%). Conclusion. The clinical implication for our findings suggests the assessment and incorporation of both skin and joint components may be advisable.
KW - Joint
KW - Key Indexing Terms: DMARD
KW - Patient-reported outcome measures
KW - Psoriasis
KW - Psoriatic arthritis
KW - Skin
UR - http://www.scopus.com/inward/record.url?scp=85102932344&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85102932344&partnerID=8YFLogxK
U2 - 10.3899/JRHEUM.190422
DO - 10.3899/JRHEUM.190422
M3 - Article
C2 - 32358158
AN - SCOPUS:85102932344
SN - 0315-162X
VL - 48
SP - 376
EP - 384
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 3
ER -