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Mechanisms underlying DMARD inefficacy in difficult-to-treat rheumatoid arthritis: a narrative review with systematic literature search.
Roodenrijs, Nadia M T; Welsing, Paco M J; van Roon, Joël; Schoneveld, Jan L M; van der Goes, Marlies C; Nagy, György; Townsend, Michael J; van Laar, Jacob M.
Afiliación
  • Roodenrijs NMT; Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht.
  • Welsing PMJ; Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht.
  • van Roon J; Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht.
  • Schoneveld JLM; Department of Rheumatology, Bravis Hospital, Roosendaal.
  • van der Goes MC; Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht.
  • Nagy G; Department of Rheumatology, Meander Medical Center, Amersfoort, The Netherlands.
  • Townsend MJ; Department of Rheumatology & Clinical Immunology.
  • van Laar JM; Department of Genetics, Cell and Immunobiology, Semmelweis University, Budapest, Hungary.
Rheumatology (Oxford) ; 61(9): 3552-3566, 2022 08 30.
Article en En | MEDLINE | ID: mdl-35238332
ABSTRACT
Management of RA patients has significantly improved over the past decades. However, a substantial proportion of patients is difficult-to-treat (D2T), remaining symptomatic after failing biological and/or targeted synthetic DMARDs. Multiple factors can contribute to D2T RA, including treatment non-adherence, comorbidities and co-existing mimicking diseases (e.g. fibromyalgia). Additionally, currently available biological and/or targeted synthetic DMARDs may be truly ineffective ('true' refractory RA) and/or lead to unacceptable side effects. In this narrative review based on a systematic literature search, an overview of underlying (immune) mechanisms is presented. Potential scenarios are discussed including the influence of different levels of gene expression and clinical characteristics. Although the exact underlying mechanisms remain largely unknown, the heterogeneity between individual patients supports the assumption that D2T RA is a syndrome involving different pathogenic mechanisms.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / Productos Biológicos / Antirreumáticos Límite: Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / Productos Biológicos / Antirreumáticos Límite: Humans Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2022 Tipo del documento: Article