Inflammatory bowel disease and psoriasis: modernizing the multidisciplinary approach
Autor: | Mona Ståhle, M Eberhardson, E Sonkoly, C R H Hedin |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Disease Gastroenterology and Hepatology 030204 cardiovascular system & hematology Gut flora Inflammatory bowel disease 03 medical and health sciences 0302 clinical medicine Psoriasis Internal Medicine medicine Genetic predisposition Gastroenterologi Humans Epigenetics Crohn's disease biology business.industry psoriasis ulcerative colitis Crohn’ s disease biologic drugs medicine.disease biology.organism_classification Inflammatory Bowel Diseases Ulcerative colitis digestive system diseases 030104 developmental biology Immunology business |
Zdroj: | Journal of internal medicineReferences. 290(2) |
ISSN: | 1365-2796 |
Popis: | Psoriasis and inflammatory bowel disease (IBD) are immune-mediated diseases occurring in barrier organs whose main task is to protect the organism from attack. These disorders are highly prevalent especially in northern Europe where psoriasis has a prevalence of around 3-4% and IBD around 0.3%. The prevalence of IBD in North America has been estimated at around 0.4%. The total incidence rates in northern Europe have been estimated at around 6 for Crohns disease and 11 for ulcerative colitis per 100 000 person-years, compared with an incidence rate of around 280 per 100 000 person-years for psoriasis. Both diseases are less common in countries with a lower index of development. The rise in IBD appears to occur as populations adopt a westernized lifestyle, whereas psoriasis seems more stable and prevalence differences may derive more from variation in genetic susceptibility. The gut microbiota is clearly an important driver of IBD pathogenesis; in psoriasis, changes in gut and skin microbiota have been reported, but it is less clear whether and how these changes contribute to the pathogenesis. Large studies show that most identified genes are involved in the immune system. However, psoriasis and IBD are highly heterogeneous diseases and there is a need for more precise and deeper phenotyping to identify specific subgroups and their genetic, epigenetic and molecular signatures. Epigenetic modifications of DNA such as histone modifications, noncoding RNA effects on transcription and translation and DNA methylation are increasingly recognized as the mechanism underpinning much of the gene-environment interaction in the pathogenesis of both IBD and psoriasis. Our understanding of underlying pathogenetic mechanisms has deepened fundamentally over the past decades developing hand in hand with novel therapies targeting pathways and proinflammatory cytokines incriminated in disease. There is not only substantial overlap between psoriasis and IBD, but also there are differences with implication for therapy. In psoriasis, drugs targeting interleukin-23 and interleukin-17 have shown superior efficacy compared with anti-TNFs, whilst in IBD, drugs targeting interleukin-17 may be less beneficial. The therapeutic toolbox for psoriasis is impressive and is enlarging also for IBD. Still, there are unmet needs reflecting the heterogeneity of both diseases and there is a need for closer molecular diagnostics to allow for the development of precise therapeutics. Funding Agencies|Stockholm CountyStockholm County Council; Swedish Medical Society; MagTarm Fund; Bengt Ihre Fund; Ruth and Richard Julins Foundation; Nanna Svartz Foundation; Stockholm County (ALF); Bengt Ihre Foundation; Swedish Medical Research CouncilSwedish Medical Research Council (SMRC)European Commission; Stockholm County Council (ALF)Stockholm County Council; Swedish Psoriasis Foundation (Psoriasisfonden); Hudfonden; National Psoriasis Foundation (USA); Psoriasis Foundation |
Databáze: | OpenAIRE |
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