PT - JOURNAL ARTICLE AU - LAURA C. COATES AU - AIZAD MUMTAZ AU - PHILIP S. HELLIWELL AU - PHILIP J. MEASE AU - KRISTINA CALLIS-DUFFIN AU - GERALD G. KRUEGER AU - NEIL J. McHUGH AU - VIBEKE STRAND AU - DAFNA D. GLADMAN AU - OLIVER FITZGERALD TI - Development of a Disease Severity and Responder Index for Psoriatic Arthritis (PsA) — Report of the OMERACT 10 PsA Special Interest Group AID - 10.3899/jrheum.110278 DP - 2011 Jul 01 TA - The Journal of Rheumatology PG - 1496--1501 VI - 38 IP - 7 4099 - http://www.jrheum.org/content/38/7/1496.short 4100 - http://www.jrheum.org/content/38/7/1496.full SO - J Rheumatol2011 Jul 01; 38 AB - Work within the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) to develop and validate composite disease activity measures in PsA has progressed. At the Outcome Measures in Rheumatology Clinical Trials (OMERACT) 8 meeting, a core set of domains to be assessed in randomized controlled trials (RCT) and longitudinal observational studies (LOS) of PsA was agreed upon. At OMERACT 10, work to date regarding proposed composite responder indices was presented. Five proposed composite responder definitions for PsA were reviewed and discussed including new data from the GRACE (GRAppa Composite Exercise) study. There was agreement that the work to date was promising, and that developing composite outcome measures for use in RCT and LOS was important. Further work was required, including data on followup timepoints and less common phenotypes of PsA, to ensure that all subgroups were represented within GRACE. During discussion on the concept of composite measures for PsA, based on predominant/little/no involvement in several domains (such as skin versus joints, enthesitis, dactylitis, spondyloarthritis) it was acknowledged that a simple summative score encompassing all domains of PsA would be difficult to construct psychometrically and may not be appropriate. Ideally, any composite measure should retain the ability to differentiate between activity in individual domains, such as enthesitis or skin psoriasis, so that the influence of each can be assessed independently. Further work is required within the GRACE dataset to develop an optimal composite measure for PsA. Several proposals to date have shown preliminary validity according to the OMERACT filter.