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ArticleClinical rheumatology2026

SYNOLACTATE-PLUS cross-sectional study: prospective validation of RESAS and synovial biomarkers in septic arthritis diagnosis.

Olivia Berthoud, Claude Bendavid, Anais Boguenet, Jean-David Albert, Géraldine Bart, Pascal Guggenbuhl, Guillaume Coiffier, François Robin

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Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Olivia Berthoud *Rheumatology Department, Rennes University Hospital, 16 Boulevard de Bulgarie, 35000, Rennes, France.
Claude Bendavid *Clinical Biochemistry and Toxicology Laboratory, Rennes University Hospital Centre, Rennes, France.
Anais BoguenetRheumatology Department, Rennes University Hospital, 16 Boulevard de Bulgarie, 35000, Rennes, France.
Jean-David AlbertRheumatology Department, Rennes University Hospital, 16 Boulevard de Bulgarie, 35000, Rennes, France.
Géraldine BartDepartment of Internal Medicine and Rheumatology, Percy National Army Training Hospital, Clamart, France.
Pascal GuggenbuhlRheumatology Department, Rennes University Hospital, 16 Boulevard de Bulgarie, 35000, Rennes, France.
Guillaume CoiffierRheumatology Department, Dinan Hospital, Dinan, France.
François RobinRheumatology Department, Rennes University Hospital, 16 Boulevard de Bulgarie, 35000, Rennes, France. francois.robin@chu-rennes.fr.ORCID http://orcid.org/0000-0001-5134-8160

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveProspective validation of the RESAS score and its components (glucose, lactate, and lactate/glucose ratio) for the diagnosis of septic arthritis. A secondary objective was to assess the diagnostic performance of additional synovial fluid (SF) biomarkers, including calprotectin, synovial CRP and total proteins.

methodsSynovial fluid samples from patients with acute arthritis (< 30 days) were prospectively collected in the monocentric, cross-sectional SYNOLACTATE-PLUS study. Septic arthritis of native joints (SANJ) was defined according to Newman's criteria. Each sample underwent Gram staining, white blood cell count, bacterial culture and crystal analysis. Biochemical measurements included L-lactate, glucose, CRP, calprotectin and total proteins. RESAS was calculated for each patient. Diagnostic performance was evaluated using ROC curves, area under the curve (AUC), sensitivity (Se), specificity (Sp), and likelihood ratios (LR ±).

resultsAmong 208 patients, 31 had SANJ, 117 crystal-induced arthritis, and 60 other inflammatory forms. RESAS achieved an AUC of 0.905 (0.836-0.975), Se 51.6%, Sp 97.2%, LR + 18.3, and LR- 0.50 at a threshold ≥  + 4. Calprotectin showed the best diagnostic accuracy (AUC 0.944, Se 93.6%, Sp 79.4%, LR + 4.5, LR- 0.08, threshold ≥ 500 mg/L). Synovial CRP (AUC 0.753) and total proteins (AUC 0.634) were not clinically relevant. A modified RESAS combining RESAS, calprotectin, and neutrophil percentage yielded improved performance (AUC 0.961, Se 93.6%, Sp 88.0%, LR + 7.8, LR- 0.07).

conclusionRESAS demonstrated strong prospective validity for predicting septic arthritis. Among protein biomarkers, synovial calprotectin showed the highest diagnostic accuracy.

Indexed as

CalprotectinGlucoseLactateScoreSeptic arthritisSynovial fluid

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