Comparison of plasma/serum levels of procalcitonin between infection and febrile disease flare in patients with systemic lupus erythematosus: a meta-analysis

Rheumatol Int. 2017 Dec;37(12):1991-1998. doi: 10.1007/s00296-017-3827-x. Epub 2017 Oct 3.

Abstract

Currently published data regarding the potential role of procalcitonin (PCT) for the discrimination between systemic lupus erythematosus (SLE) flare and infection are contradictory. To derive a more precise evaluation, a meta-analysis was performed. Published literatures from PubMed, Embase, and the Cochrane Library were obtained. The Newcastle-Ottawa Scale was used to assess the study quality. Pooled standard mean difference (SMD) with 95% confidence interval (CI) was calculated by random-effect model analysis. Heterogeneity test was performed by the Q statistic and quantified using I 2. Eight studies including 205 SLE flare patients and 198 SLE patients with infection were finally incorporated in the meta-analysis after examining title, type, abstracts, and full text. No significant differences in plasma/serum PCT levels were found between SLE patients with flare and SLE patients with infection when all studies were pooled into the meta-analysis (pooled SMD = - 0.45, 95% CI = - 0.96 to 0.06). However, subgroup analysis showed that Asian SLE patients with infection had higher plasma/serum PCT levels when compared with SLE patients with flare (p < 0.001). Overall, there is no significant difference in plasma/serum PCT levels between SLE patients with flare and SLE patients with infection. However, plasma/serum PCT levels are significantly higher in Asian SLE patients with infection.

Keywords: Infection; Meta-analysis; Procalcitonin; Systemic lupus erythematosus.

Publication types

  • Meta-Analysis

MeSH terms

  • Asian People
  • Bacterial Infections / blood*
  • Bacterial Infections / diagnosis
  • Biomarkers / blood
  • Calcitonin / blood*
  • Cross-Sectional Studies
  • Female
  • Fever / blood*
  • Fever / immunology
  • Humans
  • Lupus Erythematosus, Systemic / blood*
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / physiopathology
  • Male
  • Prospective Studies
  • Risk Factors
  • Symptom Flare Up*

Substances

  • Biomarkers
  • Calcitonin