Derivation of a Multivariable Psoriatic Arthritis Risk Estimation Tool (PRESTO): A Step Towards Prevention

Author:

Eder Lihi1ORCID,Lee Ker‐Ai2,Chandran Vinod3ORCID,Widdifield Jessica4ORCID,Drucker Aaron M.5,Ritchlin Christopher6ORCID,Rosen Cheryl F.3,Cook Richard J.2,Gladman Dafna D.3ORCID

Affiliation:

1. Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada, and Department of Medicine University of Toronto Toronto Ontario Canada

2. Department of Statistics and Actuarial Science University of Waterloo Waterloo Ontario Canada

3. Department of Medicine, University of Toronto, and Schroder Arthritis Institute, Krembil Research Institute Toronto Western Hospital Toronto Ontario Canada

4. Sunnybrook Research Institute, Sunnybrook Hospital, and Institute for Clinical Evaluative Sciences (ICES), and Institute of Health Policy, Management and Evaluation University of Toronto Toronto Ontario Canada

5. Women's College Research Institute, Women's College Hospital, and Department of Medicine, University of Toronto, and ICES, and Institute of Health Policy, Management and Evaluation University of Toronto Toronto Ontario Canada

6. Division of Rheumatology University of Rochester Rochester New York

Abstract

ObjectiveA simple, scalable tool that identifies psoriasis patients at high risk for developing psoriatic arthritis (PsA) could improve early diagnosis. We aimed to develop a risk prediction model for the development of PsA and to assess its performance among patients with psoriasis.MethodsWe analyzed data from a prospective cohort of psoriasis patients without PsA at enrollment. Participants were assessed annually by a rheumatologist for the development of PsA. Information about their demographics, psoriasis characteristics, comorbidities, medications, and musculoskeletal symptoms was used to develop prediction models for PsA. Penalized binary regression models were used for variable selection while adjusting for psoriasis duration. Risks of developing PsA over 1‐ and 5‐year time periods were estimated. Model performance was assessed by the area under the curve (AUC) and calibration plots.ResultsAmong 635 psoriasis patients, 51 and 71 developed PsA during the 1‐year and 5‐year follow‐up periods, respectively. The risk of developing PsA within 1 year was associated with younger age, male sex, family history of psoriasis, back stiffness, nail pitting, joint stiffness, use of biologic medications, patient global health, and pain severity (AUC 72.3). The risk of developing PsA within 5 years was associated with morning stiffness, psoriatic nail lesion, psoriasis severity, fatigue, pain, and use of systemic nonbiologic medication or phototherapy (AUC 74.9). Calibration plots showed reasonable agreement between predicted and observed probabilities.ConclusionsThe development of PsA within clinically meaningful time frames can be predicted with reasonable accuracy for psoriasis patients using readily available clinical variables.image

Funder

Krembil Foundation

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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