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The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis

Anti-Borrelia antibodies in the cerebrospinal fluid (CSF) are required for definite diagnosis of Lyme neuroborreliosis (LNB). However, children often present with early LNB, and antibody production in the CSF may not be demonstrated. Recent studies have suggested the chemokine CXCL13 to be an early...

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Autores principales: Henningsson, Anna J., Lager, Malin, Brännström, Rebecka, Tjernberg, Ivar, Skogman, Barbro H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154094/
https://www.ncbi.nlm.nih.gov/pubmed/30083887
http://dx.doi.org/10.1007/s10096-018-3334-3
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author Henningsson, Anna J.
Lager, Malin
Brännström, Rebecka
Tjernberg, Ivar
Skogman, Barbro H.
author_facet Henningsson, Anna J.
Lager, Malin
Brännström, Rebecka
Tjernberg, Ivar
Skogman, Barbro H.
author_sort Henningsson, Anna J.
collection PubMed
description Anti-Borrelia antibodies in the cerebrospinal fluid (CSF) are required for definite diagnosis of Lyme neuroborreliosis (LNB). However, children often present with early LNB, and antibody production in the CSF may not be demonstrated. Recent studies have suggested the chemokine CXCL13 to be an early marker for LNB. The aim of the study was to evaluate CXCL13 for laboratory diagnosis in pediatric LNB patients and to evaluate the association with pleocytosis in CSF, clinical features, and recovery. CSF samples were collected from LNB patients, classified as definite LNB (n = 44) or possible LNB (n = 22), and controls classified as non-LNB (n = 102) or other specific diagnoses (n = 23). CSF samples were analyzed with the recomBead CXCL13 assay (Mikrogen Diagnostik, Germany), cut-off 160 pg/mL. CXCL13 was significantly higher in LNB patients compared to controls (p < 0.001). Among LNB patients, 58/66 had elevated CXCL13, and among controls, 111/125 had CXCL13 levels under cut-off (sensitivity 88%, specificity 89%). In LNB patients with pleocytosis but no detectable anti-Borrelia antibodies in CSF (possible LNB), CXCL13 was elevated in 16/22 (73%). A weak correlation between CXCL13 and pleocytosis in CSF was found in LNB patients (Rho = 0.46, p < 0.01), but no differences in CXCL13 levels in relation to specific clinical features. In conclusion, CXCL13 is elevated in CSF in children with LNB, showing acceptable sensitivity and specificity. In patients with possible LNB, CXCL13 was elevated in a majority of cases (73%) and is suggested as a complementary diagnostic tool in pediatric LNB patients. CXCL13 was not associated with specific clinical features or recovery.
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spelling pubmed-61540942018-10-10 The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis Henningsson, Anna J. Lager, Malin Brännström, Rebecka Tjernberg, Ivar Skogman, Barbro H. Eur J Clin Microbiol Infect Dis Original Article Anti-Borrelia antibodies in the cerebrospinal fluid (CSF) are required for definite diagnosis of Lyme neuroborreliosis (LNB). However, children often present with early LNB, and antibody production in the CSF may not be demonstrated. Recent studies have suggested the chemokine CXCL13 to be an early marker for LNB. The aim of the study was to evaluate CXCL13 for laboratory diagnosis in pediatric LNB patients and to evaluate the association with pleocytosis in CSF, clinical features, and recovery. CSF samples were collected from LNB patients, classified as definite LNB (n = 44) or possible LNB (n = 22), and controls classified as non-LNB (n = 102) or other specific diagnoses (n = 23). CSF samples were analyzed with the recomBead CXCL13 assay (Mikrogen Diagnostik, Germany), cut-off 160 pg/mL. CXCL13 was significantly higher in LNB patients compared to controls (p < 0.001). Among LNB patients, 58/66 had elevated CXCL13, and among controls, 111/125 had CXCL13 levels under cut-off (sensitivity 88%, specificity 89%). In LNB patients with pleocytosis but no detectable anti-Borrelia antibodies in CSF (possible LNB), CXCL13 was elevated in 16/22 (73%). A weak correlation between CXCL13 and pleocytosis in CSF was found in LNB patients (Rho = 0.46, p < 0.01), but no differences in CXCL13 levels in relation to specific clinical features. In conclusion, CXCL13 is elevated in CSF in children with LNB, showing acceptable sensitivity and specificity. In patients with possible LNB, CXCL13 was elevated in a majority of cases (73%) and is suggested as a complementary diagnostic tool in pediatric LNB patients. CXCL13 was not associated with specific clinical features or recovery. Springer Berlin Heidelberg 2018-08-06 2018 /pmc/articles/PMC6154094/ /pubmed/30083887 http://dx.doi.org/10.1007/s10096-018-3334-3 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Henningsson, Anna J.
Lager, Malin
Brännström, Rebecka
Tjernberg, Ivar
Skogman, Barbro H.
The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis
title The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis
title_full The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis
title_fullStr The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis
title_full_unstemmed The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis
title_short The chemokine CXCL13 in cerebrospinal fluid in children with Lyme neuroborreliosis
title_sort chemokine cxcl13 in cerebrospinal fluid in children with lyme neuroborreliosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154094/
https://www.ncbi.nlm.nih.gov/pubmed/30083887
http://dx.doi.org/10.1007/s10096-018-3334-3
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