Abstract

Interleukin-6 (IL-6) plays a crucial role in systemic autoimmunity and pathologic inflammation. Numerous studies have explored serum IL-6 levels in systemic lupus erythematosus (SLE) and their correlation with disease activity. Here, we performed a meta-analysis to quantitatively assess the correlation between the serum IL-6 levels and SLE activity.The PubMed and EMBASE databases were thoroughly searched for relevant studies up to September 2019. Standardized mean differences (SMDs) with 95% confidence intervals (95% CIs) were used to describe the differences between serum IL-6 levels in SLE patients and healthy controls and between those in active SLE patients and inactive SLE patients. The correlation between the serum IL-6 levels and disease activity was evaluated using Fisher’s z values.A total of 24 studies involving 1817 SLE patients and 874 healthy controls were included in this meta-analysis. Serum IL-6 levels were significantly higher in SLE patients than in the healthy controls (pooled SMD: 2.12, 95% CI: 1.21-3.03, Active SLE patients had higher serum IL-6 levels than inactive SLE patients (pooled SMD: 2.12, 95% CI: 1.21-3.03). Furthermore, the pooled Fisher’s z values (pooled Fisher’s z=0.36, 95% CI: 0.26-0.46, p<0.01) showed that there was a positive correlation between the serum IL-6 levels and SLE activity.This study suggested that serum IL-6 levels were higher in patients with SLE than in healthy controls, and they were positively correlated with disease activity when Systemic Lupus Erythematosus Disease Activity Index>4 was defined as active SLE. More homogeneous studies with large sample sizes are warranted to confirm our findings due to several limitations in our meta-analysis.

Highlights

  • Systemic lupus erythematosus (SLE) is a common inflammatory autoimmune disease that mainly occurs in reproductive age women [1]

  • We found that the serum IL-6 level was markedly higher in SLE patients than in healthy controls (Figure 2)

  • We found that the serum IL-6 level was significantly higher in active SLE patients than in the inactive SLE patients (Figure 3)

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Summary

Introduction

Systemic lupus erythematosus (SLE) is a common inflammatory autoimmune disease that mainly occurs in reproductive age women [1]. SLE can impair all organ systems, resulting in serious morbidities [2]. Its etiology remains elusive, it has been widely accepted that autoantibody production, immune complex deposition, and complement activation play key roles in SLE pathogenesis. No potential conflict of interest was reported. Received for publication on February 22, 2020. Accepted for publication on June 8, 2020

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