Application of composite disease activity scores in psoriatic arthritis to the PRESTA data set

被引:51
作者
FitzGerald, Oliver [1 ]
Helliwell, Philip [2 ]
Mease, Philip [3 ,4 ]
Mumtaz, Aizad
Coates, Laura [2 ]
Pedersen, Ronald [5 ]
Nab, Henk [6 ]
Molta, Charles [5 ]
机构
[1] Univ Coll Dublin, St Vincents Univ Hosp, Dept Rheumatol, Bone & Joint Unit, Dublin 2, Ireland
[2] Univ Leeds, Leeds Inst Mol Med, Sect Musculoskeletal Dis, Leeds, W Yorkshire, England
[3] Univ Washington, Sch Med, Seattle, WA USA
[4] Swedish Med Ctr, Seattle, WA USA
[5] Pfizer Inc, Dept Stat, Collegeville, PA USA
[6] Pfizer Europe, Dept Rheumatol, Rome, Italy
关键词
RHEUMATOID-ARTHRITIS;
D O I
10.1136/annrheumdis-2011-200093
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objective This study aimed to compare the performances of the Modified Composite Psoriatic Disease Activity Index (mCPDAI) and the Disease Activity index for PSoriatic Arthritis (DAPSA) in an interventional study of etanercept in psoriatic arthritis. Methods The components of the CPDAI and DAPSA were extracted using PRESTA (Psoriasis Randomized Etanercept STudy in subjects with psoriatic Arthritis) study data. Data for four of the five domains of the CPDAI-thus an mCPDAI-were available: joints, skin, dactylitis and enthesitis (spinal involvement was not assessed). Domains in the calculation of DAPSA were subjected to global assessment of pain, swollen and tender joint counts, and C reactive protein. Subjects were randomised to etanercept 50 mg weekly (n=373) or 50 mg twice weekly (n=379) for 12 weeks; all subjects then received etanercept 50 mg weekly for 12 weeks. The performance of the scores at baseline and on weeks 12 and 24 was compared between the two treatment regimens. Results The mCPDAI and DAPSA could distinguish response to treatment comparing baseline and 12-week or 24-week values (p<0.0001). The mCPDAI, not DAPSA, could distinguish response between the two treatment groups at 12 weeks (p=0.0492), but not at 24 weeks. All domains evaluated contributed to the data variability of the mCPDAI; the most significant were dactylitis (r=0.64) and enthesitis (r=0.60). Conclusion In psoriatic arthritis with severe skin involvement, the mCPDAI was able to distinguish treatment response between the two etanercept doses. DAPSA, while demonstrating improvement in both groups over time, was unable to distinguish response between the different doses of etanercept. Further studies are needed to confirm the sensitivity of both indexes.
引用
收藏
页码:358 / 362
页数:5
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