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Efficacy of N-Acetylcysteine as an Adjuvant Therapy for Rheumatoid Arthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Authors: He T, Ren K, Xiang L, et al.
Journal: British journal of hospital medicine (London, England : 2005)
Published online: November 18, 2024
Participants: 204
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A meta-analysis of 4 RCTs involving 204 patients evaluated N-acetylcysteine efficacy as adjunctive RA therapy. NAC reduced disease activity by DAS28-ESR and decreased inflammatory markers. Improvement in joint tenderness and swelling was noted. Effect on oxidative stress was not confirmed. NAC may be a useful addition to baseline therapy.

Abstract

Rheumatoid arthritis (RA) is an inflammatory autoimmune disease and N-acetylcysteine (NAC) is considered a potential therapeutic agent for RA due to strong antioxidant and anti-inflammatory properties. Therefore, this systematic review and meta-analysis aimed to evaluate the efficacy of NAC as an adjuvant therapy for RA. A systematic search was conducted across five databases from inception to 1 August 2024, including CINAHL, Cochrane Library, EMBASE, PubMed, and Web of Science. The Cochrane risk-of-bias tool for randomized trials was used to assess the quality of the included studies. Sensitivity analysis was performed when significant heterogeneity was identified. Four studies involving 204 patients were included in our meta-analysis. The results indicated that NAC alleviated disease activity in RA patients (Disease Activity Score 28-erythrocyte sedimentation rate (DAS28-ESR): mean difference (MD) = 0.54). Additionally, NAC reduced inflammatory markers (erythrocyte sedimentation rate (ESR): MD = 3.00). However, the beneficial effects of NAC on oxidative stress in RA patients were not observed. This meta-analysis demonstrated the efficacy of NAC in reducing inflammatory markers, improving joint tenderness, and swelling in patients with RA.

MeSH Terms

humansacetylcysteinearthritis, rheumatoidrandomized controlled trials as topicantioxidantsblood sedimentationtreatment outcome
DOI: 10.12968/hmed.2024.0560
PubMed ID: 39618229