Synovial fluid D-lactate – a pathogen-specific biomarker for septic arthritis: a prospective multicenter study
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Svetlana Karbysheva
, Paula Morovic
, Petri Bellova , Marvin Sven Berger , Maik Stiehler , Sebastian Meller , Stephanie Kirschbaum , Philippe Lindenlaub , Armin Zgraggen , Michael Oberle , Michael Fuchs , Carsten Perka , Andrej Trampuz und Anna Conen
Abstract
Objectives
The performance of synovial fluid biomarker D-lactate to diagnose septic arthritis (SA) and differentiate it from crystal-induced arthritis (CA), other non-infectious rheumatic joint diseases (RD) and osteoarthrosis (OA) was evaluated.
Methods
Consecutive adult patients undergoing synovial fluid aspiration due to joint pain were prospectively included in different German and Swiss centers. Synovial fluid was collected for culture, leukocyte count and differentiation, detection of crystals, and D-lactate concentration. Youden’s J statistic was used to determine optimal D-lactate cut-off value on the receiver operating characteristic (ROC) curve by maximizing sensitivity and specificity.
Results
In total 231 patients were included. Thirty-nine patients had SA and 192 aseptic arthritis (56 patients with OA, 68 with CA, and 68 with RD). The median concentration of synovial fluid D-lactate was significantly higher in patients with SA than in those with OA, CA, and RD (p<0.0001, p<0.0001 and p<0.0001, respectively). The optimal cut-off of synovial fluid D-lactate to diagnose SA was 0.033 mmol/L with a sensitivity of 92.3 % and specificity of 85.4 % independent of previous antimicrobial treatment. Sensitivity and specificity of synovial fluid leukocyte count at a cut-off of 20,000 cells/µL was 81.1 % and 80.8 %, respectively.
Conclusions
Synovial fluid D-lactate showed a high performance for diagnosing SA which was superior to synovial fluid leukocyte count. Given its high sensitivity and specificity, it serves as both an effective screening tool for SA and a differentiator between SA and RD, especially CA.
Acknowledgments
We thank the study nurse, Cornelia Krismer, for the support in data acquisition, as well as the laboratory staff handling in the Cantonal Hospital Aarau, and the study nurse, Anne Schützer, for helping with establishing and maintaining the study infrastructure in the Center of Orthopaedics and Traumatology, University Hospital Carl Gustav Carus, Dresden.
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Research ethics: Approval of the respective Institutional Review Boards (EA1/026/20, EKNZ 2020-00438, BO-EK-431092021, FSta 40/20) was available. The study was done in accordance with the Declaration of Helsinki.
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Informed consent: Informed consent was obtained from all individuals included in this study, or their legal guardians or wards.
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Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: The authors state no conflict of interest.
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Research funding: None declared.
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Data availability: The raw data can be obtained on request from the corresponding author.
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Supplementary Material
This article contains supplementary material (https://doi.org/10.1515/cclm-2024-0556).
© 2024 Walter de Gruyter GmbH, Berlin/Boston
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