Abstract

BackgroundRheumatoid arthritis (RA) is a systemic inflammatory autoimmune disease. The pharmacological therapy of RA is often symptomatic to mitigate pain and immobility with analgesics and drugs with defined side effects and risks. Complementary medicines might decrease the signs of RA and reduce the need for them. In the present study, the anti-rheumatic, anti-inflammatory, and anti-oxidant effects of Urtica dioica and Evening Primrose Oil (EPO), in patients with RA was investigated. MethodsThis randomized, double‐blind, controlled trial involved 90 RA patients, and randomly assigned them into EPO, Urtica dioica, and placebo groups. The potential effect of these herbal medicines on Disease Activity Score (DAS) 28, Visual Analogue Scale (VAS), Total Anti-oxidant Capacity (TAC), IL-17, Rheumatoid Factor (RF), anti-cyclic citrullinated peptide antibodies (Anti-CCP), C Reactive Protein (CRP), and Erythrocyte Sedimentation Rate (ESR) before and after clinical trial were evaluated. ResultsAfter a three-month follow-up, the mean values of DAS28, IL-17, TAC, RF, and CRP in EPO and Urtica dioica groups were significantly different from the placebo group. However, the VAS, Anti-CCP, and ESR at baseline and at the end of the study were not significantly different between the three groups. After the intervention, the within-group DAS28 in the EPO and Urtica dioica groups, and placebo groups reduced significantly compared to the baseline. ConclusionMedicinal plants EPO and Urtica dioica appeared to decrease inflammatory factors, and can improve the symptoms of RA. Thus, EPO and Urtica dioica have great potential as complementary therapy in RA patients.

Highlights

  • Rheumatoid arthritis (RA) is a systemic inflammatory autoimmune disease

  • After a three month follow up, the mean values of DAS28, IL-17, Total Anti-oxidant Capacity (TAC), Rheumatoid Factor (RF), and C Reactive Protein (CRP) in Evening Primrose Ogil (EPO) and Urtica dioica groups were significantly different from the placebo group

  • The present study was conducted to examine the effect of EPO and Urtica dioica on the clinical symptoms, laboratory parameters, TAC and IL-17 in patients with RA in a period of 3 months

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Summary

Introduction

Rheumatoid arthritis (RA) is a systemic inflammatory autoimmune disease. The pharmacological therapy of RA is often symptomatic to mitigate pain and inability with analgesics and drugs with defined side effects and risks. RA characterized by an inflammatory polyarthritis that commonly involved the small joints (Guo et al, 2018), synovial inflammation, arthralgia, swelling, redness, autoantibody production, cartilage and bone damage, cardiovascular, pulmonary, and skeletal complications, that can cause progressive disability (Sung et al, 2019). Th17 cells express the cytokines such as IL-17, IL-21, and IL-22, and have been shown to play a major role in the development of inflammation and joints injury in RA. Previous studies have demo nstrated a significant role for Th17 cells and IL-17 in the pathogenesis of inflammatory and ruinous patterns properties of joint and correlation with disease activity and severity (Al-Saadany et al, Taams, 2020, Robert and Miossec, 2019)

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