TY - JOUR
T1 - Inflammatory Markers in Cerebrospinal Fluid from Patients with Hydrocephalus
T2 - A Systematic Literature Review
AU - Lolansen, Sara Diana
AU - Rostgaard, Nina
AU - Oernbo, Eva Kjer
AU - Juhler, Marianne
AU - Simonsen, Anja Hviid
AU - MacAulay, Nanna
N1 - Copyright © 2021 Sara Diana Lolansen et al.
PY - 2021
Y1 - 2021
N2 - Objective: The aim of this systematic review was to evaluate existing literature on inflammatory markers in CSF from patients with hydrocephalus and identify potential markers capable of promoting hydrocephalus development and progression.Methods: Relevant studies published before December 3rd 2020 were identified from PubMed, Embase, and reference lists. Studies were screened for eligibility using the predefined inclusion and exclusion criteria. Data from eligible studies were extracted, and sources of bias were evaluated. We included articles written in English investigating inflammatory markers in CSF from patients with hydrocephalus and control subjects. The review was conducted according to the PRISMA guidelines by three independent reviewers.Results: Twenty-two studies analyzed CSF from 311 patients with idiopathic normal pressure hydrocephalus (iNPH), 178 with posthemorrhagic hydrocephalus (PHH), 151 with other hydrocephalus diagnoses, and 394 control subjects. Fifty-eight inflammatory markers were investigated. The CSF of iNPH patients had increased CSF levels of IL-6, IL-1β, and LRG compared with control subjects, whereas the CSF of PHH patients had increased levels of IL-6, IL-18, and VEGF. CSF from patients with "other hydrocephalus diagnoses" had elevated IFN-γ compared to control subjects, and VEGF was increased in congenital hydrocephalus, spina bifida, and hydrocephalus associated with tuberculous meningitis compared with controls.Conclusion: IL-6, IL-1β, LRG, IL-18, VEGF, and IFN-γ are elevated in CSF from patients with hydrocephalus and may be involved in promotion of hydrocephalus development and progression. They may serve as novel disease biomarkers, and their signaling pathways may represent targets for pharmacological management of hydrocephalus.
AB - Objective: The aim of this systematic review was to evaluate existing literature on inflammatory markers in CSF from patients with hydrocephalus and identify potential markers capable of promoting hydrocephalus development and progression.Methods: Relevant studies published before December 3rd 2020 were identified from PubMed, Embase, and reference lists. Studies were screened for eligibility using the predefined inclusion and exclusion criteria. Data from eligible studies were extracted, and sources of bias were evaluated. We included articles written in English investigating inflammatory markers in CSF from patients with hydrocephalus and control subjects. The review was conducted according to the PRISMA guidelines by three independent reviewers.Results: Twenty-two studies analyzed CSF from 311 patients with idiopathic normal pressure hydrocephalus (iNPH), 178 with posthemorrhagic hydrocephalus (PHH), 151 with other hydrocephalus diagnoses, and 394 control subjects. Fifty-eight inflammatory markers were investigated. The CSF of iNPH patients had increased CSF levels of IL-6, IL-1β, and LRG compared with control subjects, whereas the CSF of PHH patients had increased levels of IL-6, IL-18, and VEGF. CSF from patients with "other hydrocephalus diagnoses" had elevated IFN-γ compared to control subjects, and VEGF was increased in congenital hydrocephalus, spina bifida, and hydrocephalus associated with tuberculous meningitis compared with controls.Conclusion: IL-6, IL-1β, LRG, IL-18, VEGF, and IFN-γ are elevated in CSF from patients with hydrocephalus and may be involved in promotion of hydrocephalus development and progression. They may serve as novel disease biomarkers, and their signaling pathways may represent targets for pharmacological management of hydrocephalus.
KW - Biomarkers/cerebrospinal fluid
KW - Case-Control Studies
KW - Disease Progression
KW - Female
KW - Gene Expression Regulation
KW - Glycoproteins/cerebrospinal fluid
KW - Humans
KW - Hydrocephalus/cerebrospinal fluid
KW - Inflammation
KW - Interferon-gamma/cerebrospinal fluid
KW - Interleukin-18/cerebrospinal fluid
KW - Interleukin-1beta/cerebrospinal fluid
KW - Interleukin-6/cerebrospinal fluid
KW - Male
KW - Signal Transduction
KW - Vascular Endothelial Growth Factor A/cerebrospinal fluid
UR - http://www.scopus.com/inward/record.url?scp=85100897680&partnerID=8YFLogxK
U2 - 10.1155/2021/8834822
DO - 10.1155/2021/8834822
M3 - Review
C2 - 33613789
SN - 0278-0240
VL - 2021
SP - 8834822
JO - Disease Markers
JF - Disease Markers
M1 - 8834822
ER -