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Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk
Psoriasis vulgaris is a genetically heterogenous disease with unclear molecular background. We assessed the association of psoriasis and its main clinical phenotypes with common variants of three potential psoriasis susceptibility genes: ZNF750, RPTOR and TRAF31P2. We genotyped 10 common variants in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955134/ https://www.ncbi.nlm.nih.gov/pubmed/24005976 http://dx.doi.org/10.1007/s00403-013-1407-9 |
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author | Dębniak, T. Soczawa, E. Boer, M. Różewicka-Czabańska, M. Wiśniewska, J. Serrano-Fernandez, P. Mirecka, A. Paszkowska-Szczur, K. Lubinski, J. Krysztoforska, L. Adamski, Z. Maleszka, R. |
author_facet | Dębniak, T. Soczawa, E. Boer, M. Różewicka-Czabańska, M. Wiśniewska, J. Serrano-Fernandez, P. Mirecka, A. Paszkowska-Szczur, K. Lubinski, J. Krysztoforska, L. Adamski, Z. Maleszka, R. |
author_sort | Dębniak, T. |
collection | PubMed |
description | Psoriasis vulgaris is a genetically heterogenous disease with unclear molecular background. We assessed the association of psoriasis and its main clinical phenotypes with common variants of three potential psoriasis susceptibility genes: ZNF750, RPTOR and TRAF31P2. We genotyped 10 common variants in a cohort of 1,034 case–control individuals using Taqman genotyping assays and sequencing. Minor alleles of all four TRAF3IP2 variants were more frequent among cases. The strongest, significant association was observed for rs33980500 (OR = 2.5, p = 0.01790). Minor allele of this SNP was always present in two haplotypes found to be associated with increased psoriasis risk: rs13196377_G + rs13190932_G + rs33980500_T + rs13210247_A (OR = 2.7, p = 0.0054) and rs13196377_A + rs13190932_A + rs33980500_T + rs13210247_G (OR = 1.8, p = 0.0008). Analyses of clinically relevant phenotypes revealed association of rs33980500 with pustular psoriasis (OR = 1.2, p = 0.0109). We observed significant connection of severity of cutaneous disease with variation at rs13190932 and suggestive with three remaining TRAF3IP2 SNPs. Another positive associations were found between age of onset and familial aggregation of disease: smoking and younger age of onset, smoking and occurrence of pustular psoriasis, nail involvement and arthropatic psoriasis, nail involvement and more severe course of psoriasis. We found no statistically significant differences in the prevalence of the examined variants of RPTOR and ZNF750 genes among our cases and controls. We have replicated the association of TRAF3IP2-_rs33980500 variant with the susceptibility to psoriasis. We have found new associations with clinically relevant subphenotypes such as pustular psoriasis or moderate-to-severe cases. We ascertain no connection of RPTOR and ZNF750 variants with psoriasis or its subphenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00403-013-1407-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3955134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-39551342014-03-24 Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk Dębniak, T. Soczawa, E. Boer, M. Różewicka-Czabańska, M. Wiśniewska, J. Serrano-Fernandez, P. Mirecka, A. Paszkowska-Szczur, K. Lubinski, J. Krysztoforska, L. Adamski, Z. Maleszka, R. Arch Dermatol Res Original Paper Psoriasis vulgaris is a genetically heterogenous disease with unclear molecular background. We assessed the association of psoriasis and its main clinical phenotypes with common variants of three potential psoriasis susceptibility genes: ZNF750, RPTOR and TRAF31P2. We genotyped 10 common variants in a cohort of 1,034 case–control individuals using Taqman genotyping assays and sequencing. Minor alleles of all four TRAF3IP2 variants were more frequent among cases. The strongest, significant association was observed for rs33980500 (OR = 2.5, p = 0.01790). Minor allele of this SNP was always present in two haplotypes found to be associated with increased psoriasis risk: rs13196377_G + rs13190932_G + rs33980500_T + rs13210247_A (OR = 2.7, p = 0.0054) and rs13196377_A + rs13190932_A + rs33980500_T + rs13210247_G (OR = 1.8, p = 0.0008). Analyses of clinically relevant phenotypes revealed association of rs33980500 with pustular psoriasis (OR = 1.2, p = 0.0109). We observed significant connection of severity of cutaneous disease with variation at rs13190932 and suggestive with three remaining TRAF3IP2 SNPs. Another positive associations were found between age of onset and familial aggregation of disease: smoking and younger age of onset, smoking and occurrence of pustular psoriasis, nail involvement and arthropatic psoriasis, nail involvement and more severe course of psoriasis. We found no statistically significant differences in the prevalence of the examined variants of RPTOR and ZNF750 genes among our cases and controls. We have replicated the association of TRAF3IP2-_rs33980500 variant with the susceptibility to psoriasis. We have found new associations with clinically relevant subphenotypes such as pustular psoriasis or moderate-to-severe cases. We ascertain no connection of RPTOR and ZNF750 variants with psoriasis or its subphenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00403-013-1407-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2013-09-05 2014 /pmc/articles/PMC3955134/ /pubmed/24005976 http://dx.doi.org/10.1007/s00403-013-1407-9 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Dębniak, T. Soczawa, E. Boer, M. Różewicka-Czabańska, M. Wiśniewska, J. Serrano-Fernandez, P. Mirecka, A. Paszkowska-Szczur, K. Lubinski, J. Krysztoforska, L. Adamski, Z. Maleszka, R. Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk |
title | Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk |
title_full | Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk |
title_fullStr | Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk |
title_full_unstemmed | Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk |
title_short | Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk |
title_sort | common variants of znf750, rptor and traf3ip2 genes and psoriasis risk |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955134/ https://www.ncbi.nlm.nih.gov/pubmed/24005976 http://dx.doi.org/10.1007/s00403-013-1407-9 |
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