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CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis
Background: Psoriasis can present different phenotypes and could affect diverse body areas. In contrast to the high effectiveness of biological drugs in the treatment of trunk and extremities plaque psoriasis, in palmoplantar phenotypes and in plaque scalp psoriasis, these same drugs usually have re...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506507/ https://www.ncbi.nlm.nih.gov/pubmed/36143237 http://dx.doi.org/10.3390/jpm12091452 |
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author | Reolid, Alejandra Sahuquillo-Torralba, Antonio Sanz-García, Ancor Botella-Estrada, Rafael Muñoz-Aceituno, Ester Llamas-Velasco, Mar García-Martínez, Jorge Daudén, Esteban Abad-Santos, Francisco Ovejero-Benito, María C. |
author_facet | Reolid, Alejandra Sahuquillo-Torralba, Antonio Sanz-García, Ancor Botella-Estrada, Rafael Muñoz-Aceituno, Ester Llamas-Velasco, Mar García-Martínez, Jorge Daudén, Esteban Abad-Santos, Francisco Ovejero-Benito, María C. |
author_sort | Reolid, Alejandra |
collection | PubMed |
description | Background: Psoriasis can present different phenotypes and could affect diverse body areas. In contrast to the high effectiveness of biological drugs in the treatment of trunk and extremities plaque psoriasis, in palmoplantar phenotypes and in plaque scalp psoriasis, these same drugs usually have reduced efficacy. Anti-TNF drugs could induce the appearance of palmoplantar pustulosis (PPP) in patients with other inflammatory diseases. The objective of this study is to identify if there are DNA Copy Number Variations (CNVs) associated with these different clinical phenotypes, which could justify the differences found in clinical practice. Moreover, we intend to elucidate if anti-TNF-induced PPP has a similar genetic background to idiopathic PPP. Methods: Skin samples were collected from 39 patients with different patterns of psoriasis and six patients with anti-TNF-induced PPP. The CNVs were obtained from methylation array data (Illumina Infinium Human Methylation) using the conumee R package. Results: No significant CNVs were found between the different phenotypes and the locations of psoriasis compared. Nevertheless, we found two significant bins harboring five different genes associated with anti-TNF-induced PPP in patients with a different background other than psoriasis. Conclusions: Our results may help to predict which patients could develop anti-TNF-induced PPP. |
format | Online Article Text |
id | pubmed-9506507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95065072022-09-24 CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis Reolid, Alejandra Sahuquillo-Torralba, Antonio Sanz-García, Ancor Botella-Estrada, Rafael Muñoz-Aceituno, Ester Llamas-Velasco, Mar García-Martínez, Jorge Daudén, Esteban Abad-Santos, Francisco Ovejero-Benito, María C. J Pers Med Article Background: Psoriasis can present different phenotypes and could affect diverse body areas. In contrast to the high effectiveness of biological drugs in the treatment of trunk and extremities plaque psoriasis, in palmoplantar phenotypes and in plaque scalp psoriasis, these same drugs usually have reduced efficacy. Anti-TNF drugs could induce the appearance of palmoplantar pustulosis (PPP) in patients with other inflammatory diseases. The objective of this study is to identify if there are DNA Copy Number Variations (CNVs) associated with these different clinical phenotypes, which could justify the differences found in clinical practice. Moreover, we intend to elucidate if anti-TNF-induced PPP has a similar genetic background to idiopathic PPP. Methods: Skin samples were collected from 39 patients with different patterns of psoriasis and six patients with anti-TNF-induced PPP. The CNVs were obtained from methylation array data (Illumina Infinium Human Methylation) using the conumee R package. Results: No significant CNVs were found between the different phenotypes and the locations of psoriasis compared. Nevertheless, we found two significant bins harboring five different genes associated with anti-TNF-induced PPP in patients with a different background other than psoriasis. Conclusions: Our results may help to predict which patients could develop anti-TNF-induced PPP. MDPI 2022-09-04 /pmc/articles/PMC9506507/ /pubmed/36143237 http://dx.doi.org/10.3390/jpm12091452 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Reolid, Alejandra Sahuquillo-Torralba, Antonio Sanz-García, Ancor Botella-Estrada, Rafael Muñoz-Aceituno, Ester Llamas-Velasco, Mar García-Martínez, Jorge Daudén, Esteban Abad-Santos, Francisco Ovejero-Benito, María C. CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis |
title | CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis |
title_full | CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis |
title_fullStr | CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis |
title_full_unstemmed | CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis |
title_short | CNVs Associated with Different Clinical Phenotypes of Psoriasis and Anti-TNF-Induced Palmoplantar Pustulosis |
title_sort | cnvs associated with different clinical phenotypes of psoriasis and anti-tnf-induced palmoplantar pustulosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506507/ https://www.ncbi.nlm.nih.gov/pubmed/36143237 http://dx.doi.org/10.3390/jpm12091452 |
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