Genetic control of psoriasis is relatively distinct from that of metabolic syndrome and coronary artery disease
Psoriasis is a common chronic inflammatory skin disease, associated with significant comorbidity, for example, metabolic syndrome (MetS) and coronary heart disease (CHD). This association implies that the risk to develop these diseases is commonly controlled or that the presence of one disease favou...
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Published in | Experimental dermatology Vol. 22; no. 8; pp. 552 - 553 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Denmark
Blackwell Publishing Ltd
01.08.2013
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Subjects | |
Online Access | Get full text |
ISSN | 0906-6705 1600-0625 1600-0625 |
DOI | 10.1111/exd.12192 |
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Summary: | Psoriasis is a common chronic inflammatory skin disease, associated with significant comorbidity, for example, metabolic syndrome (MetS) and coronary heart disease (CHD). This association implies that the risk to develop these diseases is commonly controlled or that the presence of one disease favours manifestation of the other. Therefore, we assessed the catalogue of genome‐wide association studies (GWAS) to analyse whether psoriasis, MetS and CHD share susceptibility loci. Interestingly, genetic control of psoriasis is almost completely independent from both MetS and CHD. In contrast, MetS and CHD share 10 common loci. Like by GWAS analysis, psoriasis susceptibility genes showed close clustering in Ingenuity Pathway Analysis, while genes conferring susceptibility to MetS and CHD were interlinked separately. These findings lead to the hypothesis that the clinically observed co‐occurrence of psoriasis with MetS and CHD may be due to a common environmental factor, for example, diet, which is known as a risk factor for all of these diseases. |
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Bibliography: | ark:/67375/WNG-NVRD580B-N Figure S1. Overlap of the genetic susceptibility of metabolic syndrome, coronary heart disease and psoriasis identified by Ingenuity Pathway Analysis. Susceptibility genes of metabolic syndrome (MetS), coronary heart disease (CHD), and psoriasis were subject to Ingenuity Pathway Analysis. This showed a tight interaction of MetS and CHD, whereas psoriasis susceptibility genes clustered relatively independently. Susceptibility genes for MetS are shown in blue, those of CHD and psoriasis are denoted in yellow or orange, respectively. Genes overlapping with MetS and CHD are in green, and genes encoding for all three diseases are in purple. The insert displays what the individual symbols correspond to. The IPA software computes the connections among the different genes based on several databases, such as HPRD (http://www.hprd.org) and BIND (http://bind.ca). The direction is also computed based on reposited experimental data. Abbreviations used: PP=Protein-Protein interaction, PD=Protein-DNA interaction, A=Activation, T=Transcription, E=Expression, and P=Phosphorylation. Genes, Environment and Inflammation - No. GRK 1743/1 istex:B82F62F5704AD523EB60C9D12C2DB6E5BE45D64E Deutsche Forschungsgemeinschaft: Excellence Cluster Inflammation - No. EXC306/1 and 2 ArticleID:EXD12192 Modulation of Autoimmunity - No. GRK1727/1 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Correspondence-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 0906-6705 1600-0625 1600-0625 |
DOI: | 10.1111/exd.12192 |