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. 2019 May;36(3):290-297.
doi: 10.1111/pde.13772. Epub 2019 Feb 21.

A retrospective cohort study to evaluate the development of comorbidities, including psychiatric comorbidities, among a pediatric psoriasis population

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A retrospective cohort study to evaluate the development of comorbidities, including psychiatric comorbidities, among a pediatric psoriasis population

Amy S Paller et al. Pediatr Dermatol. 2019 May.

Abstract

Background/objective: Compared with the adult psoriasis population, knowledge about the incidence of comorbidities in the pediatric psoriasis population is limited. The objective of this study was to assess the prevalence and incidence of comorbidities, including psychiatric comorbidities, in patients with pediatric psoriasis.

Methods: In this claims-based, retrospective cohort study, patients with pediatric psoriasis were matched 1:3 with a nonpsoriasis cohort based on age, sex, and index date (the earliest of inpatient claims or the latter of two outpatient claims).

Results: Obesity, serious infection, and juvenile idiopathic arthropathy had higher prevalence and incidence rates in the psoriasis cohort than the nonpsoriasis cohort. Psychiatric comorbidities were also more common in the psoriasis cohort than the nonpsoriasis cohort, as were ulcerative colitis and Crohn disease. Stratifying the psoriasis cohort by disease severity-mild and moderate-to-severe-found no differences in incidence rates of comorbidities between the two subsets.

Conclusion: The incidence rates of many comorbid conditions were higher for patients with pediatric psoriasis compared with patients without pediatric psoriasis, and similar between patients with moderate-to-severe and mild pediatric psoriasis.

Keywords: inflammatory disorders; psoriasis; therapy-systemic.

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Conflict of interest statement

A.S. Paller has been an investigator without personal compensation for AbbVie, Amgen Inc., Celgene, Janssen, Leo, and Novartis; and a consultant with honorarium for Amgen Inc., Eli Lilly, Novartis, and UCB. J. Schenfeld is a contract worker for Amgen Inc. and receives salary from Amgen Inc. through DOCS Global, Inc. N.A. Accortt and G. Kricorian are employees and shareholders of Amgen Inc.

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References

    1. Burden‐Teh E, Thomas KS, Ratib S, et al. The epidemiology of childhood psoriasis: a scoping review. Br J Dermatol. 2016;174:1242‐1257. - PubMed
    1. Gelfand JM, Weinstein R, Porter SB, et al. Prevalence and treatment of psoriasis in the United Kingdom: a population‐based study. Arch Dermatol. 2005;141:1537‐1541. - PubMed
    1. Olsen AO, Grjibovski A, Magnus P, et al. Psoriasis in Norway as observed in a population‐based Norwegian twin panel. Br J Dermatol. 2005;153:346‐351. - PubMed
    1. Paller AS, Mercy K, Kwasny MJ, et al. Association of pediatric psoriasis severity with excess and central adiposity: an international cross‐sectional study. JAMA Dermatol. 2013;149:166‐176. - PMC - PubMed
    1. Augustin M, Glaeske G, Radtke MA, et al. Epidemiology and comorbidity of psoriasis in children. Br J Dermatol. 2010;162:633‐636. - PubMed