TY - JOUR
T1 - Pathophysiological Mechanisms Underlying Idiopathic Normal Pressure Hydrocephalus
T2 - A Review of Recent Insights
AU - Bonney, Phillip A.
AU - Briggs, Robert G.
AU - Wu, Kevin
AU - Choi, Wooseong
AU - Khahera, Anadjeet
AU - Ojogho, Brandon
AU - Shao, Xingfeng
AU - Zhao, Zhen
AU - Borzage, Matthew
AU - Wang, Danny J.J.
AU - Liu, Charles
AU - Lee, Darrin J.
N1 - Publisher Copyright:
Copyright © 2022 Bonney, Briggs, Wu, Choi, Khahera, Ojogho, Shao, Zhao, Borzage, Wang, Liu and Lee.
PY - 2022/4/28
Y1 - 2022/4/28
N2 - The pathophysiologic mechanisms underpinning idiopathic normal pressure hydrocephalus (iNPH), a clinically diagnosed dementia-causing disorder, continue to be explored. An increasing body of evidence implicates multiple systems in the pathogenesis of this condition, though a unifying causative etiology remains elusive. Increased knowledge of the aberrations involved has shed light on the iNPH phenotype and has helped to guide prognostication for treatment with cerebrospinal fluid diversion. In this review, we highlight the central role of the cerebrovasculature in pathogenesis, from hydrocephalus formation to cerebral blood flow derangements, blood-brain barrier breakdown, and glymphatic pathway dysfunction. We offer potential avenues for increasing our understanding of how this disease occurs.
AB - The pathophysiologic mechanisms underpinning idiopathic normal pressure hydrocephalus (iNPH), a clinically diagnosed dementia-causing disorder, continue to be explored. An increasing body of evidence implicates multiple systems in the pathogenesis of this condition, though a unifying causative etiology remains elusive. Increased knowledge of the aberrations involved has shed light on the iNPH phenotype and has helped to guide prognostication for treatment with cerebrospinal fluid diversion. In this review, we highlight the central role of the cerebrovasculature in pathogenesis, from hydrocephalus formation to cerebral blood flow derangements, blood-brain barrier breakdown, and glymphatic pathway dysfunction. We offer potential avenues for increasing our understanding of how this disease occurs.
KW - blood brain barrier (BBB) breakdown
KW - cerebral blood flow
KW - communicating hydrocephalus
KW - dementia
KW - glymphatic circulation
KW - idiopathic normal pressure hydrocephalus (iNPH)
KW - ventriculoperitoneal (VP) shunt
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UR - http://www.scopus.com/inward/citedby.url?scp=85130211118&partnerID=8YFLogxK
U2 - 10.3389/fnagi.2022.866313
DO - 10.3389/fnagi.2022.866313
M3 - Review article
AN - SCOPUS:85130211118
SN - 1663-4365
VL - 14
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
M1 - 866313
ER -