Inappropriate treatment response to DMARDs: A pathway to difficult-to-treat rheumatoid arthritis

Hongtao Guo, Li Li, Bin Liu, Peipei Lu, Zhiwen Cao, Xinyu Ji, Li Li, Guilin Ouyang, Zhixin Nie, Aiping Lyu, Cheng Lu*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

5 Citations (Scopus)

Abstract

In recent years, difficult-to-treat rheumatoid arthritis (D2T RA) has attracted significant attention from rheumatologists due to its poor treatment response and the persistent symptoms or signs experienced by patients. The therapeutic demands of patients with D2T RA are not properly met due to unclear pathogenic causes and a lack of high-quality data for current treatment options, creating considerable management difficulties with this patient population. This review describes the clinical challenges associated with disease-modifying antirheumatic drugs (DMARDs) and explores contributing factors associated with inappropriate response to DMARDs that may lead to D2T RA and related immunological dysregulation. It is now understood that D2T RA is a highly heterogeneous pathological status that involves multiple factors. These factors include but are not limited to genetics, environment, immunogenicity, comorbidities, adverse drug reactions, inappropriate drug application, poor adherence, and socioeconomic status. Besides, these factors may manifest in the selection and utilization of specific DMARDs, either individually or in combination, thereby contributing to inadequate treatment response. Finding these variables may offer hints for enhancing DMARD therapy plans and bettering the condition of D2T RA patients.

Original languageEnglish
Article number110655
JournalInternational Immunopharmacology
Volume122
DOIs
Publication statusPublished - Sept 2023

Scopus Subject Areas

  • Immunology and Allergy
  • Immunology
  • Pharmacology

User-Defined Keywords

  • Contributing factors
  • Difficult-to-treat
  • DMARDs
  • Inappropriate treatment response
  • Rheumatoid arthritis

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