Sensitivity and specificity of cerebrospinal fluid CXCL13 for diagnosing Lyme neuroborreliosis - a study on 1410 patients and review of the literature.


Journal

Journal of the neurological sciences
ISSN: 1878-5883
Titre abrégé: J Neurol Sci
Pays: Netherlands
ID NLM: 0375403

Informations de publication

Date de publication:
15 Jul 2020
Historique:
received: 29 08 2019
revised: 23 03 2020
accepted: 15 04 2020
pubmed: 29 4 2020
medline: 15 5 2021
entrez: 29 4 2020
Statut: ppublish

Résumé

The B-cell chemoattractant CXCL13 has been suggested as a cerebrospinal fluid (CSF) biomarker for Lyme neuroborreliosis (LNB). Our aim was to substantiate the value of CXCL13 in a large unselected cohort and determine a practical cut-off value to diagnose LNB. We retrospectively studied clinical and CSF data of consecutive patients who underwent CSF CXCL13 testing over a period of three years (February 2015 to January 2018) at our academic teaching hospital. Patients were classified into 12 groups according to their final diagnosis. To diagnose LNB (definite or probable/possible), definitions of the respective guideline of the German Neurological Society were applied. Of 1410 patients, 29 were diagnosed with definite LNB and 9 with probable/possible LNB. Median CXCL13 levels were highly elevated in both LNB groups (554 pg/mL and 649 pg/mL, respectively) and the group with bacterial/fungal CNS infections (410 pg/mL; n = 6), while all other groups had markedly lower median CXCL13 levels (p < .001). For definite LNB, the best CXCL13 test cut-off was 55.5 pg/mL with a sensitivity of 96.6% (95% confidence interval, CI, 80.4%-99.8%) and a specificity of 94.9% (95% CI 93.5%-95.9%). All patients with LNB showed clinical improvement after antibiotic treatment. In this large monocentric cohort, CSF CXCL13 was found to be a highly sensitive and useful marker for LNB. In conditions with low index of suspicion for LNB, CXCL13 testing may be unwarranted. A review of the literature on the sensitivity and specificity of CSF CXCL13 in the differential of LNB is provided.

Identifiants

pubmed: 32344220
pii: S0022-510X(20)30179-9
doi: 10.1016/j.jns.2020.116843
pii:
doi:

Substances chimiques

Biomarkers 0
CXCL13 protein, human 0
Chemokine CXCL13 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

116843

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that there is no conflict of interest.

Auteurs

Hannes Lintner (H)

Department of Neurology, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.

Petra Hochgatterer-Rechberger (P)

Central Laboratory, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.

Barbara Pischinger (B)

Department of Neurology, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.

Josef Seier (J)

Central Laboratory, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.

Peter Vollmann (P)

Department of Neurology, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.

Alexander Haushofer (A)

Central Laboratory, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria.

Heike Rittner (H)

Department of Anaesthesiology, University Hospital of Würzburg, Würzburg, Germany.

Claudia Sommer (C)

Department of Neurology, University Hospital of Würzburg, Würzburg, Germany.

Raffi Topakian (R)

Department of Neurology, Academic Teaching Hospital Wels-Grieskirchen, Wels, Austria. Electronic address: raffi.topakian@hotmail.com.

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Classifications MeSH