Cerebrospinal fluid CXCL13 concentration for diagnosis and monitoring of neurosyphilis in people with HIV

被引:3
|
作者
Carvalho, Ricardo de S. [1 ,2 ,5 ]
Rangel, Isabelle de C. [2 ]
Soane, Michel M. [3 ]
Bacarov, Natalia B. S. [3 ]
Herbst, Victor [4 ]
Ferry, Fernando R. A. [1 ,2 ]
机构
[1] Hosp Univ Gaffree & Guinle HUGG, Dept Med Geral DEMEG, Rio De Janeiro, Brazil
[2] Univ Fed Estado Rio De Janeiro UNIRIO, Programa Posgrad Neurol PPGNEURO, Rio De Janeiro, Brazil
[3] EUROIMMUN Brasil Med Diagnost, EUROInstitute, Sao Caetano Do Sul, Brazi, SP, Brazil
[4] EUROIMMUN AG, Antigen Detect, Lubeck, Germany
[5] Univ Fed Estado Rio Janeiro UNIRIO, Dept Neurol, Programa Posgraduacao Neurol PPGNEURO, 775 Mariz & Barros St, BR- 22270004 Rio De Janeiro, RJ, Brazil
关键词
cerebrospinal fluid; CXCL13; neurosyphilis; people with HIV; syphilis; Treponema pallidum; SYPHILIS; PENICILLIN; THERAPY; TESTS;
D O I
10.1097/QAD.0000000000003813
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: The study aimed to assess and compare cerebrospinal fluid (CSF)-CXCL13 levels in People with HIV (PWH) with suspected neurosyphilis (NS), those with syphilis but without NS, and patients without treponema infection. Additionally, it aimed to evaluate changes in CSF-CXCL13 concentrations before and after antibiotic treatment. Design: This was a prospective cohort study involving 93 PWH suspected of NS. All participants underwent lumbar puncture, with CSF-CXCL13 levels measured at baseline and during follow-up in patients diagnosed with NS. Methods: CSF-CXCL13 levels were quantified using ELISA. The Mann-Whitney U test was used to analyze differences between groups, while the Wilcoxon test assessed within subject changes. ROC curve analysis determined the diagnostic efficacy of CSF-CXCL13 for NS. Results: Significantly higher CSF-CXCL13 levels were observed in patients with NS compared to those with syphilis without NS and non-syphilis patients. Posttreatment, a decline in CSF-CXCL13 levels was noted in all NS cases. A CSF-CXCL13 threshold exceeding 60.0 pg/ml, in conjunction with reactive CSF-FTA-ABS, yielded a sensitivity of 88.9% and a specificity of 97.6% for NS diagnosis. Conclusions: CSF-CXCL13 emerges as a valuable adjunctive biomarker for detecting NS in PWH, especially in cases with nonreactive CSF-VDRL. Monitoring CSF-CXCL13 levels also appears effective in evaluating therapeutic response in PWH undergoing NS treatment.
引用
收藏
页码:657 / 668
页数:12
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