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Idiopathic normal pressure hydrocephalus may be a “Two Hit” disease: Benign external hydrocephalus in infancy followed by deep white matter ischemia in late adulthood
Author(s) -
Bradley William G.,
Bahl Gautam,
Alksne John F.
Publication year - 2006
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.20684
Subject(s) - normal pressure hydrocephalus , cerebrospinal fluid , white matter , hydrocephalus , medicine , lateral ventricles , cardiology , ischemia , fourth ventricle , pathology , anesthesia , magnetic resonance imaging , surgery , radiology , disease , dementia
Purpose To determine if normal pressure hydrocephalus (NPH) could result from decreased resorption of cerebrospinal fluid (CSF) by the arachnoidal villi, leading to benign external hydrocephalus [BEH] in infancy, followed by deep white matter ischemia (DWMI) in late adulthood (the more hydrophilic environment increasing resistance to CSF flow through the extracellular space (ECS) of the brain). Materials and Methods CSF outflow via the fourth ventricle and the ECS of the brain was mathematically modeled using a parallel electrical circuit analog. The apparent diffusion coefficient (ADC) was measured as a surrogate of the amount of water in the ECS in normals, patients with symptomatic NPH, and patients with dilated ventricles without symptoms of NPH (“pre‐NPH”). Results The electrical circuit model demonstrates increasing ventricular volume with increasing resistance to flow through the ECS of the brain. ADC measurements performed in the centrum semiovale are significantly higher in patients with NPH and “pre‐NPH” than in age‐matched controls ( P < 0.05), controlling for the same degree of DWMI indicating increased fluid in the ECS of the brain. Conclusion The electrical circuit analog and finding of increased periventricular ADC support the theory that NPH is a “two hit” disease. J. Magn. Reson. Imaging 2006. © 2006 Wiley‐Liss, Inc.