Cerebrospinal Fluid Neutrophil Gelatinase-Associated Lipocalin as a Novel Biomarker for Postneurosurgical Bacterial Meningitis: A Prospective Observational Cohort Study

被引:1
|
作者
Lin, Qingwen [1 ,2 ,3 ,4 ]
Huang, Er [1 ,2 ,3 ,4 ]
Fan, Kengna [1 ,2 ,3 ,4 ]
Zhang, Zeqin [1 ]
Shangguan, Huangcheng [5 ]
Zhang, Weiqing [1 ,2 ,3 ,4 ]
Fang, Wenhua [5 ]
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, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 1, Natl Reg Med Ctr, Dept Lab Med, Binhai Campus, Fuzhou, Peoples R China
[3] Fujian Med Univ, Affiliated Hosp 1, Fujian Key Lab Lab Med, Fuzhou, Peoples R China
[4] Fujian Med Univ, Affiliated Hosp 1, Fujian Clin Res Ctr Clin Immunol Lab Test, Fuzhou, Peoples R China
[5] Fujian Med Univ, Affiliated Hosp 1, Neurosurg Res Inst, Dept Neurosurg, Fuzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Neurosurgery; Bacterial meningitis; Neutrophil gelatinase-associated lipocalin; Diagnosis; CSF;
D O I
10.1227/neu.0000000000003021
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND OBJECTIVES:Postneurosurgical bacterial meningitis (PNBM) was a significant clinical challenge, as early identification remains difficult. This study aimed to explore the potential of neutrophil gelatinase-associated lipocalin (NGAL) as a novel biomarker for the early diagnosis of PNBM in patients who have undergone neurosurgery.METHODS:A total of 436 postneurosurgical adult patients were enrolled in this study. Clinical information, cerebrospinal fluid (CSF), and blood samples were collected. After the screening, the remaining 267 patients were divided into the PNBM and non-PNBM groups, and measured CSF and serum NGAL levels to determine the diagnostic utility of PNBM. Subsequently, patients with PNBM were categorized into gram-positive and gram-negative bacterial infection groups to assess the effectiveness of CSF NGAL in differentiating between these types of infections. We analyzed the changes in CSF NGAL expression before and after anti-infection treatment in PNBM. Finally, an additional 60 patients were included as an independent validation cohort to further validate the diagnostic performance of CSF NGAL.RESULTS:Compared with the non-PNBM group, CSF NGAL was significantly higher in the PNBM group (305.1 [151.6-596.5] vs 58.5 [30.7-105.8] ng/mL; P < .0001). The area under the curve of CSF NGAL for diagnosing PNBM was 0.928 (95% CI: 0.897-0.960), at a threshold of 119.7 ng/mL. However, there was no significant difference in serum NGAL between the 2 groups (142.5 [105.0-248.6] vs 161.9 [126.6-246.6] ng/mL, P = .201). Furthermore, CSF NGAL levels were significantly higher in patients with gram-negative bacterial infections than those with gram-positive bacteria (P = .023). In addition, CSF NGAL levels decrease after treatment compared with the initial stage of infection (P < .0001). Finally, in this validation cohort, the threshold of 119.7 ng/mL CSF NGAL shows good diagnostic performance with a sensitivity and specificity of 90% and 80%, respectively.CONCLUSION:CSF NGAL holds promise as a potential biomarker for the diagnosis, early drug selection, and efficacy monitoring of PNBM.
引用
收藏
页码:1418 / 1428
页数:11
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