ArticleJAAD international2021
Societal impact for patients with psoriasis: A nationwide Swedish register study.
Article in JAAD international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 17 citations in OpenAlex.
- CORONATE: A Novel Questionnaire to Assess the Long-Term Impact of Psoriasis on Patients' Lives.Dermatology practical & conceptual · 2026Article
- Machine learning-based prediction of PASI100 response to secukinumab in patients with psoriasis: a real-world study with SHAP interpretability analysis.Frontiers in medicine · 2026Article
- Disease severity and demographic factors in relation to subjective well being among syrian psoriasis patients.Scientific reports · 2025Article
- Generalized pustular psoriasis: a multicentric study on patient characteristics and clinical burden.Orphanet journal of rare diseases · 2025Article
- With big data comes big responsibility: Strategies for utilizing aggregated, standardized, de-identified electronic health record data for research.Clinical and translational science · 2025Article
- A population-based registry study on psoriasis-associated burden of disease in Finland.Frontiers in medicine · 2025Article
- Knowledge, attitude, and practice of psoriasis patients toward their diseases: a web-based, cross-sectional study.Frontiers in medicine · 2024Article
- Psoriasis in Northern Saudi Arabia: Clinical features and implications for quality of life.Journal of public health research · 2022Article
- Time Trends in Psoriasis and Psoriatic Arthritis Incidence from 2002 to 2016 in Taiwan: An Age-Period-Cohort Analysis.Journal of clinical medicine · 2022Article
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPsoriasis is an immune-mediated chronic inflammatory disease having a significant negative health impact. Psoriasis has societal impact; loss of productivity has been estimated at approximately 10% and it may influence the patient's financial status. Relationships between quality of life, disease severity, and cost of care need exploration. Understanding the disease burden is important for health policy and research allocation. Few studies address the research gaps in socioeconomics, comorbidity, and medication use.
objectiveObserving differences in education, income, employment status, marital status, health care consumption, and drug utilization between patients with psoriasis and matched controls.
methodsCohort study following socioeconomics and health care consumption for all psoriasis patients from the Swedish patient register. All individuals with a first diagnosis of psoriasis in outpatient or inpatient care from 2002 to 2013 were followed until death, emigration, or end of the study.
resultsOverall, 109,803 patients were included (mean age 51.2 years, 53% women) and matched with 1.08 million controls. The levels of education and income were similar, but the proportion employed was significantly lower for patients with psoriasis. There was a tendency for fewer patients with psoriasis to be married. LIMITATIONS: Generalizability, lack of primary care diagnoses, and lack of early treatments (available from 2005).
conclusionUnderstanding of the socioeconomic impact of psoriasis is extended by showing reductions in employment.
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