» Articles » PMID: 15446588

Cellular Damage and Prevention in Childhood Hydrocephalus

Overview
Journal Brain Pathol
Date 2004 Sep 28
PMID 15446588
Citations 41
Authors
Affiliations
Soon will be listed here.
Abstract

The literature concerning brain damage due to hydrocephalus, especially in children and animal models, is reviewed. The following conclusions are reached: 1. Hydrocephalus has a deleterious effect on brain that is dependent on magnitude and duration of ventriculomegaly and modified by the age of onset. 2. Animal models have many histopathological similarities to humans and can be used to understand the pathogenesis of brain damage. 3. Periventricular axons and myelin are the primary targets of injury. The pathogenesis has similarities to traumatic and ischemic white matter injury. Secondary changes in neurons reflect compensation to the stress or ultimately the disconnection. 4. Altered efflux of extracellular fluid could result in accumulation of waste products that might interfere with neuron function. Further research is needed in this as well as the blood-brain barrier in hydrocephalus. 5. Some, but not all, of the changes are preventable by shunting CSF. However, axon loss cannot be reversed, therefore shunting in a given case must be considered carefully. 6. Experimental work has so far failed to show any benefit in reducing CSF production. Pharmacologic protection of the brain, at least as a temporary measure, holds some promise but more pre-clinical research is required.

Citing Articles

Neurogenesis and glial impairments in congenital hydrocephalus: insights from a BioGlue-induced fetal lamb model.

Karakaya D, Lampe K, Encinas J, Duru S, Peiro L, Oge H Fluids Barriers CNS. 2025; 22(1):20.

PMID: 39994758 PMC: 11849300. DOI: 10.1186/s12987-025-00630-3.


Regulation of brain fluid volumes and pressures: basic principles, intracranial hypertension, ventriculomegaly and hydrocephalus.

Hladky S, Barrand M Fluids Barriers CNS. 2024; 21(1):57.

PMID: 39020364 PMC: 11253534. DOI: 10.1186/s12987-024-00532-w.


Structural Alterations of the Corpus Callosum in Children With Infantile Hydrocephalus.

Adil D, Duerden E, Eagleson R, De Ribaupierre S J Child Neurol. 2024; 39(1-2):66-76.

PMID: 38387869 PMC: 11083734. DOI: 10.1177/08830738241231343.


Lower levels of Th1 and Th2 cytokines in cerebrospinal fluid (CSF) at the time of initial CSF shunt placement in children are associated with subsequent shunt revision surgeries.

Simon T, Sedano S, Rosenberg-Hasson Y, Durazo-Arvizu R, Whitlock K, Hodor P Cytokine. 2023; 169:156310.

PMID: 37523803 PMC: 10528342. DOI: 10.1016/j.cyto.2023.156310.


Assessment of longitudinal brain development using super-resolution magnetic resonance imaging following fetal surgery for open spina bifida.

Mufti N, Chappell J, Aertsen M, Ebner M, Fidon L, Deprest J Ultrasound Obstet Gynecol. 2023; 62(5):707-720.

PMID: 37161647 PMC: 10947002. DOI: 10.1002/uog.26244.


References
1.
Del Bigio M, Massicotte E . Protective effect of nimodipine on behavior and white matter of rats with hydrocephalus. J Neurosurg. 2001; 94(5):788-94. DOI: 10.3171/jns.2001.94.5.0788. View

2.
Hidaka M, Matsumae M, Yamamura M, Tsugane R, Sato O . Glucose metabolism and protective biochemical mechanisms in a rat brain affected by kaolin-induced hydrocephalus. Childs Nerv Syst. 1997; 13(4):183-8. DOI: 10.1007/s003810050066. View

3.
LORBER J . Isosorbide in the medical treatment of infantile hydrocephalus. J Neurosurg. 1973; 39(6):702-11. DOI: 10.3171/jns.1973.39.6.0702. View

4.
JONES H, Harris N, Rocca J, Andersohn R . Progressive tissue injury in infantile hydrocephalus and prevention/reversal with shunt treatment. Neurol Res. 2000; 22(1):89-96. DOI: 10.1080/01616412.2000.11741041. View

5.
Nakano H, Bandoh K, Miyaoka M, Sato K . Evaluation of hydrocephalic periventricular radiolucency by dynamic computed tomography and xenon-computed tomography. Neurosurgery. 1996; 39(4):758-62; discussion 762-3. DOI: 10.1097/00006123-199610000-00023. View