Longitudinal analysis of inflammatory biomarkers during acute rhinosinusitis

Laryngoscope. 2017 Feb;127(2):E55-E61. doi: 10.1002/lary.26344. Epub 2016 Oct 18.

Abstract

Objective: To illuminate the pathophysiology of acute rhinosinusitis (ARS) with sequential monitoring of inflammatory biomarkers during an ARS episode and to clarify their diagnostic usability in bacterial ARS.

Study design: Inception cohort study with 50 conscripts with ARS.

Methods: We collected peripheral blood high-sensitive C-reactive protein (hs-CRP), white blood cell (WBC), procalcitonin, and nasal nitric oxide (nNO) counts at 2 to 3 and 9 to 10 days of symptoms during an ARS episode. We simultaneously gathered various clinical parameters and microbiological samples. Bacterial ARS was confirmed with a positive culture of sinus aspirate.

Results: Reciprocal correlations and a significant change in biomarker levels between the two visits suggest that ARS involves a local and systemic inflammatory response that was strongest at 2 to 3 days. High-sensitive CRP and nNO reflected responses best (52% had increased CRP levels at 2-3 days; 66% had decreased nNO levels). White blood cell and procalcitonin counts rarely exceeded the reference range. Increased local and systemic inflammatory response were linked to multiple, adenoviral, or influenza A viral etiology or the detection of bacterial ARS. Local response correlated with imaging findings of wide paranasal sinus involvement and ostiomeatal complex occlusion. At 9 to 10 days, elevated (≥ 11 mg/L) and moderately elevated (≥ 49 mg/L) hs-CRP predicted bacterial ARS well (likelihood ratio [LR]+ 3.3 and LR+ 15.8, respectively), but the sensitivity for both findings remained low.

Conclusion: Acute rhinosinusitis (particularly bacterial ARS) involves a local and systemic inflammatory response that is strongest at the beginning of symptoms. Elevated hs-CRP supports the diagnosis of bacterial ARS.

Level of evidence: 4. Laryngoscope, 2016 127:E55-E61, 2017.

Keywords: Acute rhinosinusitis; C-reactive protein; CRP; NO; bacterial; high-sensitive CRP; nasal nitric oxide; procalcitonin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adolescent
  • Biomarkers / blood*
  • C-Reactive Protein / metabolism
  • Cohort Studies
  • Female
  • Humans
  • Inflammation Mediators / blood*
  • Longitudinal Studies
  • Male
  • Rhinitis / blood*
  • Rhinitis / diagnosis*
  • Sensitivity and Specificity
  • Sinusitis / blood*
  • Sinusitis / diagnosis*
  • Statistics as Topic
  • Virus Diseases / blood*
  • Virus Diseases / diagnosis*
  • Young Adult

Substances

  • Biomarkers
  • Inflammation Mediators
  • C-Reactive Protein