Cargando…
CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients
BACKGROUND: Chemokine ligand 13 (CXCL13) is believed to play a role in the recruitment of B cells in the central nervous system during neuroinflammation. Neurosyphilis is a group of clinical syndromes of the central nervous system caused by Treponema pallidum (T. pallidum) infection. The relationshi...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909691/ https://www.ncbi.nlm.nih.gov/pubmed/27376011 http://dx.doi.org/10.1186/s40064-016-2462-4 |
_version_ | 1782437861436424192 |
---|---|
author | Zeng, Yan-Li Lin, Yi-Qiang Zhang, Ning-Ning Zou, Chao-Ning Zhang, Hui-Lin Peng, Feng Liu, Zhao-Ji Zheng, Wei-Hong Yan, Jiang-Hua Liu, Li–Li |
author_facet | Zeng, Yan-Li Lin, Yi-Qiang Zhang, Ning-Ning Zou, Chao-Ning Zhang, Hui-Lin Peng, Feng Liu, Zhao-Ji Zheng, Wei-Hong Yan, Jiang-Hua Liu, Li–Li |
author_sort | Zeng, Yan-Li |
collection | PubMed |
description | BACKGROUND: Chemokine ligand 13 (CXCL13) is believed to play a role in the recruitment of B cells in the central nervous system during neuroinflammation. Neurosyphilis is a group of clinical syndromes of the central nervous system caused by Treponema pallidum (T. pallidum) infection. The relationship between CXCL13 and neurosyphilis still needs further study. In our study, CSF and serum CXCL13 concentrations were detected among 40 neurosyphilis patients, 31 syphilis/non-neurosyphilis patients, 26 non-syphilis/other central nervous system diseases patients. Serum CXCL13 concentrations were detected in 49 healthy persons. All enrolled persons were HIV-negative. Receiver operating characteristic (ROC) analysis was performed to determine the threshold value that could distinguish neurosyphilis from syphilis. RESULTS: We found that the CSF CXCL13 concentrations and CXCL13 quotient (Q(CXCL13)) were significantly increased in neurosyphilis patients compared to syphilis/non-neurosyphilis (χ(2) = 21.802, P < 0.001) and non-syphilis patients (χ(2) = 7.677, P = 0.002). ROC curve analyses revealed that CSF CXCL13 concentrations and Q(CXCL13) could serve as valuable biomarkers for differentiating neurosyphilis from non-neurosyphilis/syphilis. CONCLUSIONS: The CSF CXCL13 and Q(CXCL13) could serve as valuable biomarkers for differentiating neurosyphilis from non-neurosyphilis/syphilis in HIV-negative patients. |
format | Online Article Text |
id | pubmed-4909691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49096912016-07-01 CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients Zeng, Yan-Li Lin, Yi-Qiang Zhang, Ning-Ning Zou, Chao-Ning Zhang, Hui-Lin Peng, Feng Liu, Zhao-Ji Zheng, Wei-Hong Yan, Jiang-Hua Liu, Li–Li Springerplus Research BACKGROUND: Chemokine ligand 13 (CXCL13) is believed to play a role in the recruitment of B cells in the central nervous system during neuroinflammation. Neurosyphilis is a group of clinical syndromes of the central nervous system caused by Treponema pallidum (T. pallidum) infection. The relationship between CXCL13 and neurosyphilis still needs further study. In our study, CSF and serum CXCL13 concentrations were detected among 40 neurosyphilis patients, 31 syphilis/non-neurosyphilis patients, 26 non-syphilis/other central nervous system diseases patients. Serum CXCL13 concentrations were detected in 49 healthy persons. All enrolled persons were HIV-negative. Receiver operating characteristic (ROC) analysis was performed to determine the threshold value that could distinguish neurosyphilis from syphilis. RESULTS: We found that the CSF CXCL13 concentrations and CXCL13 quotient (Q(CXCL13)) were significantly increased in neurosyphilis patients compared to syphilis/non-neurosyphilis (χ(2) = 21.802, P < 0.001) and non-syphilis patients (χ(2) = 7.677, P = 0.002). ROC curve analyses revealed that CSF CXCL13 concentrations and Q(CXCL13) could serve as valuable biomarkers for differentiating neurosyphilis from non-neurosyphilis/syphilis. CONCLUSIONS: The CSF CXCL13 and Q(CXCL13) could serve as valuable biomarkers for differentiating neurosyphilis from non-neurosyphilis/syphilis in HIV-negative patients. Springer International Publishing 2016-06-16 /pmc/articles/PMC4909691/ /pubmed/27376011 http://dx.doi.org/10.1186/s40064-016-2462-4 Text en © The Author(s) 2016 Open AccessThis 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 | Research Zeng, Yan-Li Lin, Yi-Qiang Zhang, Ning-Ning Zou, Chao-Ning Zhang, Hui-Lin Peng, Feng Liu, Zhao-Ji Zheng, Wei-Hong Yan, Jiang-Hua Liu, Li–Li CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients |
title | CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients |
title_full | CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients |
title_fullStr | CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients |
title_full_unstemmed | CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients |
title_short | CXCL13 chemokine as a promising biomarker to diagnose neurosyphilis in HIV-negative patients |
title_sort | cxcl13 chemokine as a promising biomarker to diagnose neurosyphilis in hiv-negative patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909691/ https://www.ncbi.nlm.nih.gov/pubmed/27376011 http://dx.doi.org/10.1186/s40064-016-2462-4 |
work_keys_str_mv | AT zengyanli cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT linyiqiang cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT zhangningning cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT zouchaoning cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT zhanghuilin cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT pengfeng cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT liuzhaoji cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT zhengweihong cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT yanjianghua cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients AT liulili cxcl13chemokineasapromisingbiomarkertodiagnoseneurosyphilisinhivnegativepatients |