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Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom
Increasing epidemiological evidence suggests independent associations between psoriasis and cardiovascular and metabolic disease. Our objective was to test the hypothesis that directly-assessed psoriasis severity relates to the prevalence of metabolic syndrome and its components. Population-based, c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278499/ https://www.ncbi.nlm.nih.gov/pubmed/22113483 http://dx.doi.org/10.1038/jid.2011.365 |
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author | Langan, Sinéad M. Seminara, Nicole M. Shin, Daniel B. Troxel, Andrea B. Kimmel, Stephen E. Mehta, Nehal N. Margolis, David J. Gelfand, Joel M. |
author_facet | Langan, Sinéad M. Seminara, Nicole M. Shin, Daniel B. Troxel, Andrea B. Kimmel, Stephen E. Mehta, Nehal N. Margolis, David J. Gelfand, Joel M. |
author_sort | Langan, Sinéad M. |
collection | PubMed |
description | Increasing epidemiological evidence suggests independent associations between psoriasis and cardiovascular and metabolic disease. Our objective was to test the hypothesis that directly-assessed psoriasis severity relates to the prevalence of metabolic syndrome and its components. Population-based, cross-sectional study using computerized medical records from The Health Improvement Network Study population included individuals aged 45-65 years with psoriasis and practice-matched controls. Psoriasis diagnosis and extent were determined using provider-based questionnaires. Metabolic syndrome was defined using National Cholesterol Education Program (NCEP) Adult Treatment Panel (ATP) III criteria. 44,715 individuals were included: 4,065 with psoriasis and 40,650 controls. 2,044 participants had mild psoriasis (≤2% body surface area (BSA)), 1,377 had moderate (3-10% BSA), and 475 had severe psoriasis (>10% BSA). Psoriasis was associated with metabolic syndrome, adjusted odds ratio (OR) 1.41 (95% CI 1.31-1.51), varying in a “dose-response” manner, from mild (adj. OR 1.22, 95% CI 1.11-1.35) to severe psoriasis (adj. OR 1.98, 95% CI 1.62-2.43). Psoriasis is associated with metabolic syndrome and the association increases with increasing disease severity. Furthermore, associations with obesity, hypertriglyceridemia and hyperglycemia increase with increasing disease severity independent of other metabolic syndrome components. These findings suggest that screening for metabolic disease should be considered for psoriasis, especially when extensive. |
format | Online Article Text |
id | pubmed-3278499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-32784992012-09-01 Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom Langan, Sinéad M. Seminara, Nicole M. Shin, Daniel B. Troxel, Andrea B. Kimmel, Stephen E. Mehta, Nehal N. Margolis, David J. Gelfand, Joel M. J Invest Dermatol Article Increasing epidemiological evidence suggests independent associations between psoriasis and cardiovascular and metabolic disease. Our objective was to test the hypothesis that directly-assessed psoriasis severity relates to the prevalence of metabolic syndrome and its components. Population-based, cross-sectional study using computerized medical records from The Health Improvement Network Study population included individuals aged 45-65 years with psoriasis and practice-matched controls. Psoriasis diagnosis and extent were determined using provider-based questionnaires. Metabolic syndrome was defined using National Cholesterol Education Program (NCEP) Adult Treatment Panel (ATP) III criteria. 44,715 individuals were included: 4,065 with psoriasis and 40,650 controls. 2,044 participants had mild psoriasis (≤2% body surface area (BSA)), 1,377 had moderate (3-10% BSA), and 475 had severe psoriasis (>10% BSA). Psoriasis was associated with metabolic syndrome, adjusted odds ratio (OR) 1.41 (95% CI 1.31-1.51), varying in a “dose-response” manner, from mild (adj. OR 1.22, 95% CI 1.11-1.35) to severe psoriasis (adj. OR 1.98, 95% CI 1.62-2.43). Psoriasis is associated with metabolic syndrome and the association increases with increasing disease severity. Furthermore, associations with obesity, hypertriglyceridemia and hyperglycemia increase with increasing disease severity independent of other metabolic syndrome components. These findings suggest that screening for metabolic disease should be considered for psoriasis, especially when extensive. 2011-11-24 2012-03 /pmc/articles/PMC3278499/ /pubmed/22113483 http://dx.doi.org/10.1038/jid.2011.365 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Langan, Sinéad M. Seminara, Nicole M. Shin, Daniel B. Troxel, Andrea B. Kimmel, Stephen E. Mehta, Nehal N. Margolis, David J. Gelfand, Joel M. Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom |
title | Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom |
title_full | Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom |
title_fullStr | Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom |
title_full_unstemmed | Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom |
title_short | Prevalence of metabolic syndrome in patients with psoriasis: A population-based study in the United Kingdom |
title_sort | prevalence of metabolic syndrome in patients with psoriasis: a population-based study in the united kingdom |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278499/ https://www.ncbi.nlm.nih.gov/pubmed/22113483 http://dx.doi.org/10.1038/jid.2011.365 |
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