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A Systematic Review Characterizing Psoriatic Arthritis Onset and Exacerbation in Patients Receiving Biologic Therapy
BACKGROUND: While biologic therapies revolutionized treatment of immune-mediated inflammatory diseases (IMIDs), some adverse effects have been noted. This includes the development and exacerbation of PsA in patients on biologic agents, however the outcomes were not extensively explored. OBJECTIVE: T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361424/ https://www.ncbi.nlm.nih.gov/pubmed/35317662 http://dx.doi.org/10.1177/12034754221088556 |
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author | Sachdeva, Muskaan Abduelmula, Abrahim Mufti, Asfandyar Georgakopoulos, Jorge R. Lytvyn, Yuliya Yeung, Jensen |
author_facet | Sachdeva, Muskaan Abduelmula, Abrahim Mufti, Asfandyar Georgakopoulos, Jorge R. Lytvyn, Yuliya Yeung, Jensen |
author_sort | Sachdeva, Muskaan |
collection | PubMed |
description | BACKGROUND: While biologic therapies revolutionized treatment of immune-mediated inflammatory diseases (IMIDs), some adverse effects have been noted. This includes the development and exacerbation of PsA in patients on biologic agents, however the outcomes were not extensively explored. OBJECTIVE: To perform a systematic review to characterize the outcomes of PsA onset or exacerbation secondary to biologic use. METHODS: MEDLINE and EMBASE search conducted on March 23, 2021 resulted in 18 studies comprised of 64 patients. RESULTS: Of the 64 patients, 57 (89.1%) experienced new-onset PsA and 7 (10.9%) experienced exacerbation of preexisting PsA following exposure to a biologic; most commonly a TNF-α inhibitor (42.2%, n = 27/64) and IL-12/23 inhibitors (39.1%, n = 25/64). The mean durations of biologic use before PsA onset and exacerbation were 14.8 months and 5.2 months, respectively. Twenty-four patients (44.4%) subsequently switched to an alternate biologic without further reports of PsA-related adverse events. All 64 patients reported a specific treatment for PsA; most commonly discontinuation of the associated biologic agent (32.8%, n = 21/64). Complete resolution of PsA was reported in 35.9% (n = 23/64) of cases, of which 91.3% (n = 21/23) resulted after discontinuation of biologic. CONCLUSION: Although we characterized outcomes of PsA induction and exacerbation secondary to biologic use, large-scale studies are required. |
format | Online Article Text |
id | pubmed-9361424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-93614242022-08-10 A Systematic Review Characterizing Psoriatic Arthritis Onset and Exacerbation in Patients Receiving Biologic Therapy Sachdeva, Muskaan Abduelmula, Abrahim Mufti, Asfandyar Georgakopoulos, Jorge R. Lytvyn, Yuliya Yeung, Jensen J Cutan Med Surg Review Articles BACKGROUND: While biologic therapies revolutionized treatment of immune-mediated inflammatory diseases (IMIDs), some adverse effects have been noted. This includes the development and exacerbation of PsA in patients on biologic agents, however the outcomes were not extensively explored. OBJECTIVE: To perform a systematic review to characterize the outcomes of PsA onset or exacerbation secondary to biologic use. METHODS: MEDLINE and EMBASE search conducted on March 23, 2021 resulted in 18 studies comprised of 64 patients. RESULTS: Of the 64 patients, 57 (89.1%) experienced new-onset PsA and 7 (10.9%) experienced exacerbation of preexisting PsA following exposure to a biologic; most commonly a TNF-α inhibitor (42.2%, n = 27/64) and IL-12/23 inhibitors (39.1%, n = 25/64). The mean durations of biologic use before PsA onset and exacerbation were 14.8 months and 5.2 months, respectively. Twenty-four patients (44.4%) subsequently switched to an alternate biologic without further reports of PsA-related adverse events. All 64 patients reported a specific treatment for PsA; most commonly discontinuation of the associated biologic agent (32.8%, n = 21/64). Complete resolution of PsA was reported in 35.9% (n = 23/64) of cases, of which 91.3% (n = 21/23) resulted after discontinuation of biologic. CONCLUSION: Although we characterized outcomes of PsA induction and exacerbation secondary to biologic use, large-scale studies are required. SAGE Publications 2022-03-22 /pmc/articles/PMC9361424/ /pubmed/35317662 http://dx.doi.org/10.1177/12034754221088556 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Articles Sachdeva, Muskaan Abduelmula, Abrahim Mufti, Asfandyar Georgakopoulos, Jorge R. Lytvyn, Yuliya Yeung, Jensen A Systematic Review Characterizing Psoriatic Arthritis Onset and Exacerbation in Patients Receiving Biologic Therapy |
title | A Systematic Review Characterizing Psoriatic Arthritis Onset
and Exacerbation in Patients Receiving Biologic
Therapy |
title_full | A Systematic Review Characterizing Psoriatic Arthritis Onset
and Exacerbation in Patients Receiving Biologic
Therapy |
title_fullStr | A Systematic Review Characterizing Psoriatic Arthritis Onset
and Exacerbation in Patients Receiving Biologic
Therapy |
title_full_unstemmed | A Systematic Review Characterizing Psoriatic Arthritis Onset
and Exacerbation in Patients Receiving Biologic
Therapy |
title_short | A Systematic Review Characterizing Psoriatic Arthritis Onset
and Exacerbation in Patients Receiving Biologic
Therapy |
title_sort | systematic review characterizing psoriatic arthritis onset
and exacerbation in patients receiving biologic
therapy |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361424/ https://www.ncbi.nlm.nih.gov/pubmed/35317662 http://dx.doi.org/10.1177/12034754221088556 |
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