Review
Prevalence of psoriatic arthritis in patients with psoriasis: A systematic review and meta-analysis of observational and clinical studies

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Background

Wide-ranging prevalence estimates of psoriatic arthritis (PsA) in patients with psoriasis have been reported.

Objectives

To assess the prevalence and incidence of PsA in patients with psoriasis.

Methods

Two authors independently searched 3 databases for studies reporting on the prevalence or incidence of PsA in patients with psoriasis. A proportion meta-analysis was performed to calculate the pooled proportion estimates of PsA in patients with psoriasis.

Results

A total of 266 studies examining 976,408 patients with psoriasis were included. Overall, the pooled proportion (95% confidence interval [CI]) of PsA among patients with psoriasis was 19.7% (95% CI, 18.5%-20.9%). In children and adolescents (<18 years of age), the pooled prevalence was 3.3% (95% CI, 2.1%-4.9%). The PsA prevalence was 22.7% (95% CI, 20.6%-25.0%) in European patients with psoriasis, 21.5% (95% CI, 15.4%-28.2%) in South American patients with psoriasis, 19.5% (95% CI, 17.1%-22.1%) in North American patients with psoriasis, 15.5% (95% CI, 0.009%-51.5%) in African patients with psoriasis, and 14.0% (95% CI, 95% CI, 11.7%-16.3%) in Asian patients with psoriasis. The prevalence of PsA was 23.8% (95% CI, 20.1%-27.6%) in studies in which the Classification Criteria for Psoriatic Arthritis were applied. The incidence of PsA among patients with psoriasis ranged from 0.27 to 2.7 per 100 person-years.

Limitations

Between-study heterogeneity may have affected the estimates.

Conclusions

We found that 1 in 4 patients with psoriasis have PsA. With the growing recognition of the Classification Criteria for Psoriatic Arthritis, more homogenous and comparable prevalence estimates are expected to be reported.

Section snippets

Literature search

This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses, and a study protocol was developed a priori.

All articles from inception of the databases through November 2017 were potentially eligible for inclusion. Two authors independently screened the 3 databases (PubMed, Web of Science, and EMBASE) using the following search terms: (psoriasis) AND (psoriatic OR arthritis OR arthropathy OR incidence OR prevalence).

Inclusion and exclusion criteria

To qualify for inclusion,

Results

We identified 6331 records through database searching (2139 in PubMed, 1217 in Web of Science, and 2975 in EMBASE); 4323 nonduplicate records were screened by title and abstract, yielding 1302 articles for full-text assessment. Counting the additional 41 studies identified by screening references, 287 studies were included for data extraction and 266 studies were selected for quantitative analysis (Fig 1); together, these studies included 976,408 patients with psoriasis (12,884 children and

Discussion

Quantitative analysis of 266 studies yielded a PsA prevalence of 19.7% among 976,408 patients with psoriasis. The prevalence of PsA was markedly lower in children and adolescents than in adults but equally frequent in both sexes. Notably, higher estimates were found in patients with moderate-to-severe psoriasis than in patients with mild psoriasis, suggesting that increased attention among this group of patients is warranted.

The prevalence of PsA among patients with psoriasis was lowest in

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    Funding sources: None.

    Disclosure: Dr Kristensen has received fees for speaking and consultancy from Pfizer, MSD, AbbVie, UCB, Eli Lilly and Company, Novartis, Celgene, Janssen Pharmaceuticals, Roche, Forward Pharma, and BMS. Dr Gladman has received consultancy fees and/or grant support from AbbVie, Amgen, BMS, Celgene, Eli Lilly and Company, Janssen, Pfizer, Novartis, and UCB. Dr Jullien has received research funding from Pfizer and honoraria as a consultant and/or speaker from Abbvie, Amgen, Celgene, Eli Lilly and Company, Janssen Pharmaceuticals, MSD, Novartis, and Pfizer. Dr Gottlieb has received honoraria as a consultant and/or speaker from Janssen Inc, Celgene Corp, Bristol-Myers Squibb, Beiersdorf Inc, Abbvie, UCB, Novartis, Incyte, Eli Lilly and Company, Reddy Labs, Valeant, Dermira, Allergan, and Sun Pharmaceutical Industries, and he has received research funding from Janssen, Incyte, Eli Lilly and Company, Novartis, Allergan, and Leo Pharma. Dr Gisondi has received honoraria as a consultant and/or speaker from AbbVie, Celgene, Eli Lilly and Company, Janssen, Leo Pharma, MSD, Novartis, Pfizer, and UCB. Dr Wu is an investigator for AbbVie, Amgen, Eli Lilly and Company, Janssen, Novartis, and Regeneron. Dr Thyssen is supported by an unrestricted grant from the Lundbeck Foundation; he has received speaker honoraria from Galderma, Sanofi-Genzyme, and MEDA; has attended advisory board meetings for Roche and Sanofi-Genzyme; and is an investigator for LEO Pharma. Dr Egeberg has received research funding from Pfizer, Eli Lilly and Company, the Danish National Psoriasis Foundation, and the Kgl Hofbundtmager Aage Bang Foundation and has received honoraria as a consultant and/or speaker from Almirall, Leo Pharma, Samsung Bioepis Co Ltd, Pfizer, Eli Lilly and Company, Novartis, Galderma, and Janssen Pharmaceuticals. Drs Alinaghi, Calov, and Coates have no conflicts of interest to disclose.

    Drs Alinaghi and Calov had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Drs Egeberg and Thyssen take responsibility for study concept and design. All the authors take responsibility for acquisition, analysis, and interpretation of the data and for critical revision of the manuscript for important intellectual content. Drs Alinaghi and Egeberg take responsibility for drafting of the manuscript. Dr Egeberg takes responsibility for statistical analysis. Drs Egeberg and Thyssen take responsibility for administrative, technical, or material support and for study supervision.

    Reprints not available from the authors.

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