Meta-analysis on the efficacy and safety of immunoadsorption for systemic lupus erythematosus among Chinese population

Clin Rheumatol. 2020 Dec;39(12):3581-3592. doi: 10.1007/s10067-020-05156-7. Epub 2020 May 28.

Abstract

To systematically evaluate the efficacy and safety of immunoadsorption (IAS) versus non-IAS for systemic lupus erythematosus (SLE) among Chinese population. A meta-analysis was performed by all the literatures germane to estimate the SLE patients treated with IAS and non-IAS from published randomized controlled trials (RCTs) from 1990 to February 2020. Mean differences (MDs), relative ratios (RRs), and 95% confidence intervals (CIs) were calculated, and the meta-analysis was conducted with Stata 12.0 software. A total of 18 RCTs involving 457 patients were included. The results of meta-analysis demonstrated that the IgG, Scr, Bun, ANA, 24-h urine protein, leptin, and TNF-α of IAS combined with a drug therapy group were lower than that of non-IAS, and the levels of C3 and C4 were higher than that of non-IAS after treatment in terms of laboratory parameters. In terms of adverse reactions, the incidence of fever or chills, low blood pressure, or bleeding risk was higher in the treatment group. However, there was no difference in the incidence of puncture point bleeding, thrombocytopenia, mild rash, death due to severe infection, tightness, palpitation, or chest tightness between the two groups. However, most of the adverse effects could be considered as tolerable after timely treatment. Our results indicate that IAS may be superior to non-IAS in treating SLE patients. However, due to the lower quality of included studies, high quality of multicenter, large sample size, randomized, and double-blind controlled trials are needed to validate the results.

Keywords: Immunoadsorption; Meta-analysis; SLE; Systematic review.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • China
  • Hemorrhage
  • Humans
  • Lupus Erythematosus, Systemic* / therapy
  • Multicenter Studies as Topic
  • Randomized Controlled Trials as Topic
  • Thrombocytopenia*