2025/03/08 by Alexandra T. Geanacopoulos, Pui Y. Lee, Todd W. Lyons +7 · 1 voice
Medicine · #Orthopedic Infections and Treatments #Infectious Diseases and Tuberculosis #Hematological disorders and diagnostics
paper · pdf · doi:10.1093/ofid/ofaf139
openalex publication_date 2025/03/08 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/29
Abstract Background Pyogenic musculoskeletal infections, such as septic arthritis and osteomyelitis, require prompt recognition and treatment but can be challenging to distinguish from Lyme or inflammatory arthritis. Our goal was to identify cytokine biomarkers of musculoskeletal infections. Methods Using 2 multicenter prospective cohorts of children undergoing emergency department evaluation for musculoskeletal infection, we selected children ≤21 years of age with a musculoskeletal infection (cases) matched by age and sex to children with Lyme and inflammatory arthritis (controls). We performed a 45-cytokine/chemokine panel using the Olink proximity extension assay platform and used receiver operator curve analysis to evaluate the discriminative ability of each cytokine. Using forward stepwise logistic regression, we derived a 3-cytokine panel and compared the accuracy with 5 commonly available plasma biomarkers. Results We included 47 children with musculoskeletal infection, 48 with Lyme arthritis, and 49 with inflammatory arthritis. Interleukin-6 had the highest accuracy for musculoskeletal infection (area under the curve [AUC], 0.84; 95% CI, 0.77–0.91). A 3-cytokine biosignature panel (interleukin-6, interleukin-17A, and colony stimulating factor–1) had the highest overall accuracy (AUC, 0.90; 95% CI, 0.84–0.96) and performed better than 5 common plasma biomarkers (white blood cell count, absolute neutrophil count, C-reactive protein, erythrocyte sedimentation rate, and procalcitonin; P < .05 for all comparisons). Conclusions Plasma cytokines can distinguish musculoskeletal infections from Lyme or inflammatory arthritis and may assist initial decision-making for children undergoing evaluation for musculoskeletal infection.