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Research ArticlePsoriatic Arthritis
Open Access

Effectiveness of Disease-Modifying Antirheumatic Drugs for Enthesitis in a Prospective Longitudinal Psoriatic Arthritis Cohort

Ashish J. Mathew, Mitchell Sutton, Daniel Pereira, Dafna D. Gladman and Vinod Chandran
The Journal of Rheumatology September 2022, 49 (9) 1020-1025; DOI: https://doi.org/10.3899/jrheum.211231
Ashish J. Mathew
1A.J. Mathew, DNB, DM, Centre for Prognosis Studies in the Rheumatic Diseases, Psoriatic Arthritis Program, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada, Division of Rheumatology, Department of Medicine, University of Toronto, Toronto, Ontario, Canada, The Copenhagen Center for Arthritis and Research (COPECARE), Center for Rheumatology and Spine Diseases, Centre of Head and Orthopedics, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark, Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark, and Department of Clinical Immunology and Rheumatology, Christian Medical College, Vellore, India;
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  • ORCID record for Ashish J. Mathew
Mitchell Sutton
2M. Sutton, MSc, D. Pereira, MSc, Centre for Prognosis Studies in the Rheumatic Diseases, Psoriatic Arthritis Program, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada;
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Daniel Pereira
2M. Sutton, MSc, D. Pereira, MSc, Centre for Prognosis Studies in the Rheumatic Diseases, Psoriatic Arthritis Program, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada;
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Dafna D. Gladman
3D.D. Gladman, MD, FRCPC, Centre for Prognosis Studies in the Rheumatic Diseases, Psoriatic Arthritis Program, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Division of Rheumatology, Department of Medicine, University of Toronto, and Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada;
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Vinod Chandran
4V. Chandran, DM, PhD, FRCPC, Centre for Prognosis Studies in the Rheumatic Diseases, Psoriatic Arthritis Program, Schroeder Arthritis Institute, Krembil Research Institute, University Health Network, Toronto, Division of Rheumatology, Department of Medicine, University of Toronto, Toronto, Institute of Medical Science, University of Toronto, Toronto, and Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
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  • ORCID record for Vinod Chandran
  • For correspondence: vinod.chandran{at}uhnresearch.ca
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Article Figures & Data

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  • Entheses (combination of SPARCC, LEI, and MASES) examined in the study. LEI: Leeds Enthesitis Index; MASES: Maastricht Ankylosing Spondylitis Enthesitis Score; SPARCC: Spondyloarthritis Research Consortium of Canada.
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    Figure 1.

    Entheses (combination of SPARCC, LEI, and MASES) examined in the study. LEI: Leeds Enthesitis Index; MASES: Maastricht Ankylosing Spondylitis Enthesitis Score; SPARCC: Spondyloarthritis Research Consortium of Canada.

Tables

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    Table 1.

    Baseline characteristics of the study patients (N = 526).

    Values
    Age, yrs49.02 (13.12)
    Males, n (%)272 (51.71)
    Duration of PsA, yrs10.74 (10.73)
    BMI, kg/m229.13 (6.25)
    PASI4.26 (8.38)
    Enthesitis score, median (IQR)2 (1-2)
    Time of enthesitis onset to resolution, months8.73 (3.48)
    Swollen joint count3.30 (5.54)
    Tender joint count7.72 (9.83)
    Actively inflamed joint counta8.88 (10.55)
    Damaged joint count4.09 (8.38)
    Axial diseaseb, n (%) (N = 476)141 (29.62)
    Dactylitis, n (%)108 (20.53)
    Nail lesions at baseline, n (%)287 (54.56)
    Fibromyalgia at baseline, n (%)127 (24.14)
    Baseline enthesitis year, n (%)
       2000-2004118 (22.43)
       2005-2009137 (26.05)
       2010-2014129 (24.52)
       > 2015142 (27.00)
    • Values are expressed as mean (SD) unless indicated otherwise.

    • ↵aActively inflamed joint count is the sum of tender and/or swollen joints.

    • ↵bAxial disease was defined as patients fulfilling the radiographic arm of the modified New York ankylosing spondylitis criteria (≥ bilateral grade 2 sacroiliitis or unilateral grade 3 or 4). PASI: Psoriasis Area and Severity Index.

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    Table 2.

    Number of patients in each category of medications with details of resolution of enthesitis (N = 526).

    Medications in Each Categoryn (%)No. of Patients on
    Each Medication (%)
    Average Time on
    Treatment, Years (SD)
    Resolution of Enthesitis, n (%)
    YesNo
    Category I142 (27.00)2.58 (3.69)117 (82.39)25 (17.61)
          No medication52 (36.66)NA
          NSAID90 (63.38)2.58 (3.69)
    Category II196 (37.26)3.06 (4.58)173 (88.26)23 (11.73)
       Methotrexate150 (76.53)a2.93 (4.61)
       Leflunomide29 (14.79)1.74 (2.82)
       Sulfasalazine32 (16.32)2.69 (3.50)
       Azathioprine10 (5.10)5.82 (7.00)
       Cyclosporine2 (1.02)2.34 (0.33)
    Category III188 (35.74)1.72 (2.23)163 (86.70)25 (13.30)
       Targeted bDMARDs
          TNFib155 (82.45)1.86 (2.39)
          IL-17ic14 (7.44)1.18 (1.09)
          IL-12/23i, IL-23i18 (9.57)0.94 (0.97)
       Targeted sDMARDs
          PDE-5i (Apremilast)1 (0.50)–
          JAKi (Tofacitinib)0 (0)–
    Total patients with and without
       resolution of enthesitis
    453 (86.12)73 (13.88)
    Male240 (52.98)41 (56.16)
    Females213 (47.02)32 (43.83)
    • ↵aPercentage of individual medications do not add to 100 as some patients were on combination cDMARDs.

    • ↵bIncludes etanercept, adalimumab, infliximab, golimumab, and certolizumab pegol.

    • ↵cIncludes secukinumab and ixekizumab. bDMARD: biologic disease-modifying antirheumatic drug; IL-17i: interleukin 17 inhibitor; IL-12/23i: interleukin 12/23 inhibitor; JAKi: Janus kinase inhibitor; NA: not applicable; NSAID: nonsteroidal antiinflammatory drug; PDE-5i: phosphodiesterase-5 inhibitor; sDMARD: synthetic disease-modifying antirheumatic drug; TNFi: tumor necrosis factor inhibitor.

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    Table 3.

    Association between treatment and resolution of enthesitis.

    Univariable ModelMultivariable Model
    OR (95% CI)POR (95% CI)P
    Sex, male1.61 (0.97-2.68)0.071.66 (0.97-2.84)0.06
    Baseline age, yrs1.00 (0.98-1.02)0.851.00 (0.98-1.02)0.98
    Baseline PsA duration, yrs1.00 (0.98-1.03)0.811.00 (0.97-1.03)0.99
    Baseline enthesitis count0.96 (0.87-1.06)0.450.97 (0.87-1.09)0.65
    Baseline actively inflamed joint count0.98 (0.96-1.00)0.030.97 (0.95-0.99)0.01
    BMI, kg/m21.01 (0.97-1.05)0.691.02 (0.97-1.06)0.49
    Nail lesions1.26 (0.76-2.08)0.371.27 (0.75-2.15)0.38
    Fibromyalgia1.01 (0.56-1.82)0.971.31 (0.69-2.47)0.41
    Medication category0.58*0.43*
       Category IRefRefRefRef
       Category II1.40 (0.74-2.63)0.301.51 (0.78-2.91)0.30
       Category III1.24 (0.67-2.31)0.501.42 (0.74-2.71)0.22
    • ↵*Global P value. OR: odds ratio; PsA: psoriatic arthritis.

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The Journal of Rheumatology
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1 Sep 2022
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Effectiveness of Disease-Modifying Antirheumatic Drugs for Enthesitis in a Prospective Longitudinal Psoriatic Arthritis Cohort
Ashish J. Mathew, Mitchell Sutton, Daniel Pereira, Dafna D. Gladman, Vinod Chandran
The Journal of Rheumatology Sep 2022, 49 (9) 1020-1025; DOI: 10.3899/jrheum.211231

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Effectiveness of Disease-Modifying Antirheumatic Drugs for Enthesitis in a Prospective Longitudinal Psoriatic Arthritis Cohort
Ashish J. Mathew, Mitchell Sutton, Daniel Pereira, Dafna D. Gladman, Vinod Chandran
The Journal of Rheumatology Sep 2022, 49 (9) 1020-1025; DOI: 10.3899/jrheum.211231
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Keywords

ANTIRHEUMATIC DRUGS
ENTHESOPATHY
PSORIATIC ARTHRITIS

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