Diagnostic value of cerebrospinal fluid Neutrophil Gelatinase-Associated Lipocalin for differentiation of bacterial meningitis from tuberculous meningitis or cryptococcal meningitis: a prospective cohort study

被引:1
|
作者
Wang, Qi [1 ,2 ,3 ,4 ]
Lin, Qingwen [1 ,2 ,3 ,4 ]
Wang, Haiyan [1 ]
Tang, Minjie [1 ,2 ,3 ,4 ]
Fan, Kengna [1 ,2 ,3 ,4 ]
Zhang, Zeqin [1 ]
Huang, Er [1 ,2 ,3 ,4 ]
Zhang, Weiqing [1 ,2 ,3 ,4 ]
Wang, Fengqing [1 ,2 ,3 ,4 ]
Ou, Qishui [1 ,2 ,3 ,4 ]
Liu, Xiaofeng [1 ,2 ,3 ,4 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 1, Gene Diag Res Ctr, Dept Lab Med, Fuzhou 350005, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Natl Reg Med Ctr, Dept Lab Med, Binhai Campus, Fuzhou 350212, Peoples R China
[3] Fujian Med Univ, Affiliated Hosp 1, Fujian Key Lab Lab Med, Fuzhou 350005, Fujian, Peoples R China
[4] Fujian Med Univ, Affiliated Hosp 1, Fujian Clin Res Ctr Clin Immunol Lab Test, Fuzhou 350005, Peoples R China
关键词
Bacterial meningitis; Neutrophil Gelatinase-Associated Lipocalin; Cerebrospinal fluid; Diagnostic biomarker; Central nervous system infection; NGAL; ORIGIN; MARKER;
D O I
10.1186/s12967-023-04485-w
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background The early differential diagnosis between bacterial meningitis (BM) and tuberculous meningitis (TBM) or cryptococcal meningitis (CM) remains a significant clinical challenge. Neutrophil Gelatinase-Associated Lipocalin (NGAL) has been reported as a novel inflammatory biomarker in the early stages of infection. This study aimed to investigate whether cerebrospinal fluid (CSF) NGAL can serve as a potential biomarker for distinguishing between BM and TBM or CM. Methods We prospectively enrolled the patients with suspected CNS infections at admission and divided them into three case groups: BM (n = 67), TBM (n = 55), CM (n = 51), and an age- and sex-matched hospitalized control (HC, n = 58). Detected the CSF NGAL and assessed its diagnostic accuracy in distinguishing between BM and TBM or CM. Additionally, longitudinally measured the CSF NGAL levels in patients with BM to evaluate its potential as a monitoring tool for antibacterial treatment. Results The concentration of CSF NGAL in BM was significantly higher than in TBM, CM, and HC (all P < 0.05), while the serum NGAL did not show significant differences among the three case groups. The ROC analysis demonstrated that CSF NGAL presented a good diagnostic performance with an AUC of 0.834 (0.770-0.886) and at the optimal cutoff value of 74.27 ng/mL with 70.15% sensitivity and 77.36% specificity for discriminating BM with TBM and CM. Additionally, the CSF NGAL in the convalescent period of BM was significantly lower than in the acute period (P < 0.05). Conclusions CSF NGAL may serve as a potential biomarker for distinguishing between acute BM and TBM or CM. Additionally, it holds clinical significance in monitoring the effectiveness of antibiotic therapy for BM.
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页数:10
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