Inflammatory marker comparison in childhood brucellosis: predicting osteoarticular involvement

Elif Böncüoğlu1,2, Şadiye Kübra Tüter Öz2, Zafer Bağcı3

  • 1Department of Pediatric Infectious Diseases, Faculty of Medicine, İzmir Democracy University Buca Seyfi Demirsoy Research and Training Hospital, İzmir, Türkiye.

Insights

In children with brucellosis, lower white blood cell counts and elevated C-reactive protein and neutrophil-monocyte ratio can indicate osteoarticular involvement. Further prospective studies are needed for validation.

Area of Science:

  • Pediatrics
  • Infectious Diseases
  • Rheumatology

Background:

  • Brucellosis complications require better diagnostic markers, especially in pediatric osteoarticular disease.
  • Limited research exists on inflammatory markers for pediatric brucellosis with osteoarticular involvement (OI).

Purpose of the Study:

  • To compare inflammatory markers in children with brucellosis, differentiating between those with and without osteoarticular involvement (OI).

Main Methods:

  • Retrospective evaluation of 38 pediatric brucellosis patients (1 month-18 years).
  • Collected data included complete blood count, inflammatory markers (neutrophil-monocyte ratio [NMR], C-reactive protein [CRP], erythrocyte sedimentation rate [ESR]), and Brucella serum agglutination test (SAT).
  • Osteoarticular involvement (OI) confirmed by MRI in symptomatic patients; comparison between OI and non-OI groups.

Main Results:

  • Patients with OI (n=9) were older and had significantly higher SAT titers (≥ 1/640) compared to those without OI.
  • Higher CRP (p=0.038) and NMR (p=0.012) levels were observed in the OI group.
  • Lower white blood cell (WBC) counts (p=0.015) were found in children with OI.

Conclusions:

  • Lower WBC counts and higher CRP and NMR levels may predict OI in pediatric brucellosis at admission.
  • Findings require validation in larger, prospective pediatric studies.
  • Highlights the utility of specific inflammatory markers in diagnosing OI in pediatric brucellosis.
Abstract