Plasma interleukin-1β, -6, -8 and tumor necrosis factor-α as highly informative markers of pelvic inflammatory disease

Shun An Lee, Hsiu Ting Tsai, Hsiu Chung Ou, Chih Ping Han, Yi Torng Tee, Yi Chen Chen, Ming Tsang Wu, Ming Chin Chou, Po Hui Wang, Shun Fa Yang

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

Background: The role of proinflammatory cytokines in pelvic inflammatory disease (PID) is unclear. We therefore determined whether plasma proinflammatory cytokines, interleukin-1β (IL-1β), IL-6, IL-8 and tumor necrosis factor-α (TNF-α) were useful plasma markers in PID patients. Methods: Multiplex bead array analysis was used to measure the plasma levels of proinflammatory cytokines in 50 healthy controls as well as in 41 PID patients before and after routine protocol treatments. Results: IL-1β, IL-6, IL-8 and TNF-α were significantly elevated in PID patients before antibiotic treatment than after treatment. However, IL-8 was not significantly different between healthy controls and PID patients. The relative increase in ratio of IL-6 was significantly correlated with white blood cell count (r=0.448, p=0.003), neutrophil count (r=0.472, p=0.002) and C-reactive protein level (r=0.412, p=0.008). Conclusions: IL-1β, IL-6, IL-8 and TNF-α may play an important role in the pathogenesis of PID. These biomarkers, particularly IL-6, could be useful adjuncts for the clinical diagnosis of PID.

Original languageEnglish
Pages (from-to)997-1003
Number of pages7
JournalClinical Chemistry and Laboratory Medicine
Volume46
Issue number7
DOIs
Publication statusPublished - Jul 1 2008
Externally publishedYes

Keywords

  • Interleukin-6 (IL-6)
  • Pelvic inflammatory disease
  • Proinflammatory cytokines

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Biochemistry, medical

Fingerprint

Dive into the research topics of 'Plasma interleukin-1β, -6, -8 and tumor necrosis factor-α as highly informative markers of pelvic inflammatory disease'. Together they form a unique fingerprint.

Cite this