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ß-D-Glucan Assay in the Cerebrospinal Fluid for the Diagnosis of Non-cryptococcal Fungal Infection of the Central Nervous System: A Retrospective Multicentric Analysis and a Comprehensive Review of the Literature

Abstract Background Except for cryptococcosis, fungal infection of the central nervous system (FI-CNS) is a rare but severe complication. Clinical and radiological signs are non-specific, and the value of conventional mycological diagnosis is very low. This study aimed to assess the value of β1,3-D-...

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Published in:Clinical infectious diseases 2023-09, Vol.77 (5), p.711-720
Main Authors: Bigot, Jeanne, Leroy, Jordan, Chouaki, Taieb, Cholley, Laurence, Bigé, Naïke, Tabone, Marie-Dominique, Brissot, Eolia, Thorez, Sophie, Maizel, Julien, Dupont, Hervé, Sendid, Boualem, Hennequin, Christophe, Guitard, Juliette
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Language:English
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Summary:Abstract Background Except for cryptococcosis, fungal infection of the central nervous system (FI-CNS) is a rare but severe complication. Clinical and radiological signs are non-specific, and the value of conventional mycological diagnosis is very low. This study aimed to assess the value of β1,3-D-glucan (BDG) detection in the cerebrospinal fluid (CSF) of non-neonatal non-cryptococcosis patients. Methods Cases associated with BDG assay in the CSF performed in 3 French University Hospitals over 5 years were included. Clinical, radiological, and mycological results were used to classify the episodes as proven/highly probable, probable, excluded, and unclassified FI-CNS. Sensitivity and specificity were compared to that calculated from an exhaustive review of the literature. Results In total, 228 episodes consisting of 4, 7, 177, and 40 proven/highly probable, probable, excluded, and unclassified FI-CNS, respectively, were analysed. The sensitivity of BDG assay in CSF to diagnose proven/highly probable/probable FI-CNS ranged from 72.7% [95% confidence interval {CI}: 43.4%‒90.2%] to 100% [95% CI: 51%‒100%] in our study and was 82% in the literature. For the first time, specificity could be calculated over a large panel of pertinent controls and was found at 81.8% [95% CI: 75.3%‒86.8%]. Bacterial neurologic infections were associated with several false positive results Conclusions Despite its sub-optimal performance, BDG assay in the CSF should be added to the diagnostic armamentarium for FI-CNS. Although presenting sub-optimal performances (sensitivity: 72.7%–100% and specificity: 81.8%), β1,3-D-glucan (BDG) assay should be added to the panel of biomarkers to test in the cerebrospinal fluid (CSF) for the challenging diagnosis of fungal infections of the CNS.
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciad274