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Targeted Therapies in Axial Psoriatic Arthritis
Specific and high-quality evidence on the efficacy of the current targeted therapies for axial disease in psoriatic arthritis (axPsA) is still scarce. Indeed, almost all the cohorts investigated in clinical trials on PsA consisted of patients with peripheral arthritis, where a small number of them a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273289/ https://www.ncbi.nlm.nih.gov/pubmed/34262600 http://dx.doi.org/10.3389/fgene.2021.689984 |
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author | Floris, Alberto Congia, Mattia Chessa, Elisabetta Angioni, Maria Maddalena Piga, Matteo Cauli, Alberto |
author_facet | Floris, Alberto Congia, Mattia Chessa, Elisabetta Angioni, Maria Maddalena Piga, Matteo Cauli, Alberto |
author_sort | Floris, Alberto |
collection | PubMed |
description | Specific and high-quality evidence on the efficacy of the current targeted therapies for axial disease in psoriatic arthritis (axPsA) is still scarce. Indeed, almost all the cohorts investigated in clinical trials on PsA consisted of patients with peripheral arthritis, where a small number of them also had axial involvement. Only one randomized controlled trial was so far specifically designed to assess the efficacy of a biological disease-modifying antirheumatic drug (DMARD) in axPsA. For other biological and synthetic targeted DMARDs, the most specific evidence for treatment in axPsA is extrapolated from post-hoc analyses based on PsA patients with concomitant peripheral and axial manifestations. Furthermore, the current trials and post-hoc analysis on axPsA are affected by major limitations, including the lack of a widely accepted definition of axPsA and the lack of specific and validated outcome measures. Finally, poor data are available on the genetics of axPsA, although alleles differentially expressed in different patterns of axPsA might offer advantages in the prospective of personalized medicine in axPsA patients. Overall, this review suggests that there is an urgent need for more reliable evidence derived from studies specifically designed for axPsA and based on a validated definition of axPsA and on specific outcome measures. |
format | Online Article Text |
id | pubmed-8273289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82732892021-07-13 Targeted Therapies in Axial Psoriatic Arthritis Floris, Alberto Congia, Mattia Chessa, Elisabetta Angioni, Maria Maddalena Piga, Matteo Cauli, Alberto Front Genet Genetics Specific and high-quality evidence on the efficacy of the current targeted therapies for axial disease in psoriatic arthritis (axPsA) is still scarce. Indeed, almost all the cohorts investigated in clinical trials on PsA consisted of patients with peripheral arthritis, where a small number of them also had axial involvement. Only one randomized controlled trial was so far specifically designed to assess the efficacy of a biological disease-modifying antirheumatic drug (DMARD) in axPsA. For other biological and synthetic targeted DMARDs, the most specific evidence for treatment in axPsA is extrapolated from post-hoc analyses based on PsA patients with concomitant peripheral and axial manifestations. Furthermore, the current trials and post-hoc analysis on axPsA are affected by major limitations, including the lack of a widely accepted definition of axPsA and the lack of specific and validated outcome measures. Finally, poor data are available on the genetics of axPsA, although alleles differentially expressed in different patterns of axPsA might offer advantages in the prospective of personalized medicine in axPsA patients. Overall, this review suggests that there is an urgent need for more reliable evidence derived from studies specifically designed for axPsA and based on a validated definition of axPsA and on specific outcome measures. Frontiers Media S.A. 2021-06-28 /pmc/articles/PMC8273289/ /pubmed/34262600 http://dx.doi.org/10.3389/fgene.2021.689984 Text en Copyright © 2021 Floris, Congia, Chessa, Angioni, Piga and Cauli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Floris, Alberto Congia, Mattia Chessa, Elisabetta Angioni, Maria Maddalena Piga, Matteo Cauli, Alberto Targeted Therapies in Axial Psoriatic Arthritis |
title | Targeted Therapies in Axial Psoriatic Arthritis |
title_full | Targeted Therapies in Axial Psoriatic Arthritis |
title_fullStr | Targeted Therapies in Axial Psoriatic Arthritis |
title_full_unstemmed | Targeted Therapies in Axial Psoriatic Arthritis |
title_short | Targeted Therapies in Axial Psoriatic Arthritis |
title_sort | targeted therapies in axial psoriatic arthritis |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273289/ https://www.ncbi.nlm.nih.gov/pubmed/34262600 http://dx.doi.org/10.3389/fgene.2021.689984 |
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