Presepsin: A potential biomarker of PJI? A comparative analysis with known and new infection biomarkers

Author:

Marazzi Monica Gioia1,Randelli Filippo2ORCID,Brioschi Marco2,Drago Lorenzo13,Romanò Carlo Luca3,Banfi Giuseppe34,Massaccesi Luca5,Crapanzano Calogero6,Morelli Franca6,Corsi Romanelli Massimiliano Marco17,Galliera Emanuela13

Affiliation:

1. Department of Biomedical Sciences for Health, Università degli Studi di Milano, Milan, Italy

2. U.O. Ortopedia e Traumatologia, IRCCS Policlinico San Donato, Milan, Italy

3. IRCCS Galeazzi Orthopedic Institute, Milan, Italy

4. Vita-Salute San Raffaele University, Milan, Italy

5. Department of Biomedical, Surgical and Oral Science, Università degli Studi di Milano, Milan, Italy

6. U.O. Patologia Clinica, Istituto Ortopedico Gaetano Pini, Milan, Italy

7. U.O.C SMEL-1 Patologia Clinica, IRCCS Policlinico San Donato, Milan, Italy

Abstract

There is still no “gold standard” for the diagnosis and prognosis of post-operative periprosthetic joint infection (PJI). Among serum biomarkers, an emerging molecule is presepsin, the soluble fraction of CD14, recently described in other settings as a powerful diagnostic tool to detect sepsis at different degrees of severity. The aim of this study was to investigate the diagnostic and prognostic value of presepsin in PJI. A total of 30 patients with PJI and 30 patients without PJI were enrolled. Presepsin, C-reactive protein (CRP), serum interleukin (IL)-6, triggering receptor expressed on myeloid cells 1 (TREM-1), CCL2, matrix metalloproteinase 9 (MMP-9), CD163, osteopontin (OPN), and toll-like receptor 2 (TLR2) were measured at different times after surgery. Receiver operating characteristic (ROC) curves and area under the curve (AUC) were analyzed for each biomarker. Presepsin showed greater diagnostic value than CRP and IL-6; CD163, TREM-1, and MMP-9 had very low diagnostic potential. Presepsin, OPN, CCL2, suPAR, and TLR2 all decreased significantly with increasing time of recovery after surgery in PJI patients. Presepsin can be considered a useful tool for the diagnosis and clinical monitoring of PJI and can be backed by a panel of new inflammatory markers involved in monocyte-/macrophage-mediated inflammatory responses, such as OPN, CCL2, TLR2, and suPAR.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

Reference37 articles.

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