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dc.contributor.authorGarcía-Porrúa, Carloses_ES
dc.contributor.authorHeras-Recuero, Elenaes_ES
dc.contributor.authorBlázquez-Sánchez, Teresaes_ES
dc.contributor.authorTores-Roselló, Arantxaes_ES
dc.contributor.authorCastañeda, Santoses_ES
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-03-06T09:11:12Z
dc.date.available2025-03-06T09:11:12Z
dc.date.issued2024es_ES
dc.identifier.issn2077-0383es_ES
dc.identifier.urihttps://hdl.handle.net/10902/35903
dc.description.abstractBackground/Objectives: Polymyalgia Rheumatica (PMR) is an inflammatory condition that primarily affects individuals aged 50 and older, especially in Western countries. Although glucocorticoids are the cornerstone of PMR treatment, these drugs are associated with side effects, making it advisable to use them for the shortest duration possible. However, tapering or discontinuation of glucocorticoids often leads to disease relapses. In this review, we focus on the traditional management of PMR, as well as the potential for therapies that may reduce glucocorticoid use. Special attention is given to the efficacy of biologic agents in PMR management. Methods: A literature review, primarily based on articles published in PubMed, was conducted. In addition to discussing various glucocorticoids and conventional disease-modifying drugs used for the management of isolated PMR, this review specifically focused on the information reported regarding new therapies, with particular emphasis on biologic agents. Results: Prednisone or prednisolone at a dose ranging between 12.5 and 25 mg/day is the agreed-upon treatment for PMR. Due to the side effects associated with prolonged glucocorticoid use and the high frequency of relapses when glucocorticoids are tapered, glucocorticoid-sparing agents have emerged as tools in the management of PMR. Methotrexate has traditionally been the conventional disease-modifying antirheumatic drug (DMARD) unanimously recommended for use in PMR. Other conventional DMARDs, such as leflunomide, have shown promising results but require further study. The use of biologic agents has marked a significant step forward in the management of PMR. While anti-TNF agents failed to provide beneficial effects in isolated PMR, anti-IL-6 receptor agents, such as tocilizumab and sarilumab, have demonstrated efficacy in reducing relapse frequency, lowering the cumulative glucocorticoid burden, and achieving long-term remission of the disease. Other biologic agents, many of which have been used in giant cell arteritis, as well as Janus kinase (JAK) inhibitors, are currently under investigation. Conclusions: Glucocorticoids are the primary treatment for isolated PMR but are associated with comorbidities, especially in patients with pre-existing conditions or frequent relapses. Glucocorticoid-sparing agents, such as methotrexate and biologics, in particular tocilizumab and sarilumab, offer alternatives, improving symptoms and reducing glucocorticoid use. While biologic agents reduce long-term side effects and help achieve disease remission, their use must consider potential side effects and higher costs compared to traditional therapies.es_ES
dc.format.extent20 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceJournal of Clinical Medicine, 2024, 13, 6492es_ES
dc.subject.otherPolymyalgia rheumaticaes_ES
dc.subject.otherRelapseses_ES
dc.subject.otherPrednisonees_ES
dc.subject.otherMethotrexatees_ES
dc.subject.otherLeflunomidees_ES
dc.subject.otherBiologic agentses_ES
dc.subject.otherTocilizumabes_ES
dc.subject.otherSarilumabes_ES
dc.subject.otherJAK inhibitorses_ES
dc.titleTraditional and emerging strategies for managing polymyalgia rheumatica: insights into new treatmentses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/jcm13216492es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/jcm13216492es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International