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Multimorbidity in Psoriasis as a Risk Factor for Psoriatic Arthritis: A Population-Based Study.
Karmacharya, Paras; Chakradhar, Rikesh; Hulshizer, Cassondra A; Gunderson, Tina M; Ogdie, Alexis; Davis, John M; Wright, Kerry; Tollefson, Megha M; Duarte-García, Alí; Bekele, Delamo; Maradit-Kremers, Hilal; Crowson, Cynthia S.
Afiliação
  • Karmacharya P; Division of Rheumatology & Immunology, Vanderbilt University Medical Center, Nashville, TN.
  • Chakradhar R; Division of Rheumatology, Mayo Clinic, Rochester, MN.
  • Hulshizer CA; Division of Rheumatology, Mayo Clinic, Rochester, MN.
  • Gunderson TM; Department of Psychiatry, MetroHealth Medical Center, Psychiatry, Cleveland, OH.
  • Ogdie A; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
  • Davis JM; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
  • Wright K; Departments of Medicine/Rheumatology and Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
  • Tollefson MM; Division of Rheumatology, Mayo Clinic, Rochester, MN.
  • Duarte-García A; Division of Rheumatology, Mayo Clinic, Rochester, MN.
  • Bekele D; Departments of Dermatology and Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN.
  • Maradit-Kremers H; Division of Rheumatology, Mayo Clinic, Rochester, MN.
  • Crowson CS; Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN.
Article em En | MEDLINE | ID: mdl-38291896
ABSTRACT

OBJECTIVES:

To examine multimorbidity in psoriasis and its association with the development of PsA.

METHODS:

A retrospective cohort study was performed using the Rochester Epidemiology Project. Population-based incidence (2000-2009) and prevalence (Jan 1, 2010) cohorts of psoriasis were identified by manual chart review. A cohort of individuals without psoriasis (comparators) were identified (11 matched on age, sex, and county). Morbidities were defined using ≥2 Clinical Classification Software codes ≥30 days apart within prior five years. PsA was defined using ClASsification of Psoriatic ARthritis (CASPAR) criteria. χ2 and rank-sum tests were used to compare morbidities, and age-, sex-, and race-adjusted Cox models to examine the association of baseline morbidities in psoriasis with development of PsA.

RESULTS:

Among 817 incident psoriasis patients, the mean age was 45.2 years with 52.0% females, and 82.0% moderate/severe psoriasis. No multimorbidity differences were found between incident psoriasis patients and comparators. However, in the 1,088 prevalent psoriasis patients, multimorbidity was significantly more common compared with 1,086 comparators (OR 1.35 and OR 1.48 for ≥2 and ≥5 morbidities, respectively). Over a median 13.3-year follow-up, 23 patients (cumulative incidence 2.9% by 15 years) developed PsA. Multimorbidity (≥2 morbidities) was associated with a 3-fold higher risk of developing PsA.

CONCLUSION:

Multimorbidity was more common in the prevalent but not incident cohort of psoriasis compared with the general population, suggesting patients with psoriasis may experience accelerated development of multimorbidity. Moreover, multimorbidity at psoriasis onset significantly increased the risk of developing PsA, highlighting the importance of monitoring multimorbid psoriasis patients for the development of PsA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Rheumatology (Oxford) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Rheumatology (Oxford) Ano de publicação: 2024 Tipo de documento: Article