» Articles » PMID: 27931942

Interleukin 6 in the Cerebrospinal Fluid As a Biomarker for Onset of Vasospasm and Ventriculitis After Severe Subarachnoid Hemorrhage

Overview
Journal World Neurosurg
Publisher Elsevier
Date 2016 Dec 10
PMID 27931942
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: The aim of the study was to investigate the diagnostic potential of interleukin 6 (IL-6) and other soluble biomarkers in serum and cerebrospinal fluid (CSF) for early diagnosis of cerebral vasospasm (cVS) and external ventricular drain-associated ventriculitis (VC) and to separate these conditions from aneurysmal subarachnoid hemorrhage (aSAH) without further complication (SAH).

Methods: The concentrations of serum biomarkers and markers in the CSF were collected in 63 consecutive patients with aSAH and external ventricular drainage. Arithmetical means and standard deviations, area under the curve (AUC), cutoff values (C-OFF), sensitivity (SE), and specificity (SP) were calculated for markers and their correlation with SAH, cVS, and VC.

Results: Clinical courses included 27 patients with cVS, 17 with VC, and 19 with SAH. Mean ± standard deviationIL-6 values were 7588 ± 4580 pg/mL at onset of VC and 4102 ± 4970 pg/mL for cVS and higher than 234 ± 239 pg/mL in SAH (P < 0.001). IL-6 showed excellent diagnostic potential for differing between VC and SAH (AUC, 1.00; C-OFF, 707; SE, 100%; SP, 100%), and a moderate diagnostic potential for differing VC from cVS (AUC, 0.757; C-OFF, 3100 pg/Ml; SE, 86.7%; SP, 70.6%). The concentration of IL-6 within the cVS group was significantly increased compared with SAH (AUC, 0.937; C-OFF, 530 pg/mL; SE, 87.5%; SP, 91.7%).

Conclusions: IL-6 is increased after aSAH in patients with cVS or VC. Patients with a IL-6 level higher than a C-OFF of 3100 pg/mL have an increased likelihood for VC; patients with IL-6 levels between 530 and 3100 pg/mL have an increased posttest probability for cVS.

Citing Articles

Novel inflammatory markers in intracerebral hemorrhage: Results from Olink proteomics analysis.

Hu Z, Chen S, Zhang E, Wei L, Wang J, Shang Q FASEB J. 2025; 39(2):e70341.

PMID: 39853806 PMC: 11760662. DOI: 10.1096/fj.202402183RR.


Multi-targeted olink proteomics analyses of cerebrospinal fluid from patients with aneurysmal subarachnoid hemorrhage.

Ding R, Wu L, Wei S, Lu H, Qin X, Liu X Proteome Sci. 2024; 22(1):11.

PMID: 39604965 PMC: 11600900. DOI: 10.1186/s12953-024-00236-x.


Meropenem pharmacokinetics in cerebrospinal fluid: comparing intermittent and continuous infusion strategies in critically ill patients-a prospective cohort study.

Wicha S, Kinast C, Munchow M, Wittova S, Greppmair S, Kunzelmann A Antimicrob Agents Chemother. 2024; 68(9):e0045124.

PMID: 39082803 PMC: 11373225. DOI: 10.1128/aac.00451-24.


Biomarkers in aneurysmal subarachnoid hemorrhage: A short review.

Batista S, Bocanegra-Becerra J, Claassen B, Rubiao F, Rabelo N, Figueiredo E World Neurosurg X. 2023; 19:100205.

PMID: 37206060 PMC: 10189293. DOI: 10.1016/j.wnsx.2023.100205.


Inflammatory Markers as Predictors of Shunt Dependency and Functional Outcome in Patients with Aneurysmal Subarachnoid Hemorrhage.

Rostgaard N, Olsen M, Capion T, MacAulay N, Juhler M Biomedicines. 2023; 11(4).

PMID: 37189615 PMC: 10135965. DOI: 10.3390/biomedicines11040997.