Adams RDFC, Hakim S et al (1965) Symptomatic occult hydrocephalus with normal cerebrospinal fluid pressure. N Engl J Med 273(3):117–126. https://doi.org/10.1056/NEJM196507152730301
Article CAS PubMed Google Scholar
Langner S, Fleck S, Baldauf J, Mensel B, Kühn J, Kirsch M (2017) Diagnosis and Differential Diagnosis of Hydrocephalus in Adults. RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 189(08):728–739. https://doi.org/10.1055/s-0043-108550
de Laurentis C, Cristaldi P, Arighi A, Cavandoli C, Trezza A, Sganzerla EP et al (2020) Role of aquaporins in hydrocephalus: what do we know and where do we stand? A systematic review. J Neurol 268(11):4078–4094. https://doi.org/10.1007/s00415-020-10122-z
Ishikawa MYS, Yamamoto K et al (2018) Astrogliosis and impaired aquaporin4 and dystrophin systems in idiopathic normal pressure hydrocephalus. Neuropathol Appl Neurobiol 44(5):474–484. https://doi.org/10.1111/nan.12420
Xiao H, Hu F, Ding J, Ye Z (2022) Cognitive Impairment in Idiopathic Normal Pressure Hydrocephalus. Neurosci Bull 38(9):1085–1096. https://doi.org/10.1007/s12264-022-00873-2
Article PubMed PubMed Central Google Scholar
Tarasoff-Conway JM, Carare RO, Osorio RS, Glodzik L, Butler T, Fieremans E et al (2015) Clearance systems in the brain-implications for Alzheimer disease. Nat Rev Neurol 11(8):457–470. https://doi.org/10.1038/nrneurol.2015.119
Article CAS PubMed PubMed Central Google Scholar
Yamada S, Mase M (2023) Cerebrospinal Fluid Production and Absorption and Ventricular Enlargement Mechanisms in Hydrocephalus. Neurologia medico-chirurgica 63(4):141–151. https://doi.org/10.2176/jns-nmc.2022-0331
Article PubMed PubMed Central Google Scholar
Cinalli G, Spennato P, Nastro A, Aliberti F, Trischitta V, Ruggiero C et al (2011) Hydrocephalus in aqueductal stenosis. Child’s Nerv Syst 27(10):1621–1642. https://doi.org/10.1007/s00381-011-1546-2
Bae YJ, Choi BS, Kim J-M, Choi J-H, Cho SJ, Kim JH (2021) Altered glymphatic system in idiopathic normal pressure hydrocephalus. Parkinsonism Relat Disord 82:56–60. https://doi.org/10.1016/j.parkreldis.2020.11.009
Article CAS PubMed Google Scholar
Georgiopoulos C, Tisell A, Holmgren RT, Eleftheriou A, Rydja J, Lundin F et al (2024) Noninvasive assessment of glymphatic dysfunction in idiopathic normal pressure hydrocephalus with diffusion tensor imaging. J Neurosurg 140(3):612–620. https://doi.org/10.3171/2023.6.Jns23260
Reeves BC, Karimy JK, Kundishora AJ, Mestre H, Cerci HM, Matouk C et al (2020) Glymphatic System Impairment in Alzheimer’s Disease and Idiopathic Normal Pressure Hydrocephalus. Trends Mol Med 26(3):285–295. https://doi.org/10.1016/j.molmed.2019.11.008
Article CAS PubMed PubMed Central Google Scholar
Iliff JJ, Wang M, Liao Y, Plogg BA, Peng W, Gundersen GA et al (2012) A Paravascular Pathway Facilitates CSF Flow Through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid β. Sci Transl Med 4(147). https://doi.org/10.1126/scitranslmed.3003748
Mestre H, Kostrikov S, Mehta Rupal I, Nedergaard M (2017) Perivascular spaces, glymphatic dysfunction, and small vessel disease. Clin Sci 131(17):2257–2274. https://doi.org/10.1042/cs20160381
Jiang D, Liu L, Kong Y, Chen Z, Rosa-Neto P, Chen K et al (2023) Regional Glymphatic Abnormality in Behavioral Variant Frontotemporal Dementia. Ann Neurol 94(3):442–456. https://doi.org/10.1002/ana.26710
Article CAS PubMed PubMed Central Google Scholar
Nakajima M, Yamada S, Miyajima M, Ishii K, Kuriyama N, Kazui H et al (2021) Guidelines for Management of Idiopathic Normal Pressure Hydrocephalus (Third Edition): Endorsed by the Japanese Society of Normal Pressure Hydrocephalus. Neurologia medico-chirurgica 61(2):63–97. https://doi.org/10.2176/nmc.st.2020-0292
Article PubMed PubMed Central Google Scholar
Shinoda N, Hirai O, Hori S, Mikami K, Bando T, Shimo D et al (2017) Utility of MRI-based disproportionately enlarged subarachnoid space hydrocephalus scoring for predicting prognosis after surgery for idiopathic normal pressure hydrocephalus: clinical research. J Neurosurg 127(6):1436–1442. https://doi.org/10.3171/2016.9.Jns161080
Taoka T, Masutani Y, Kawai H, Nakane T, Matsuoka K, Yasuno F et al (2017) Evaluation of glymphatic system activity with the diffusion MR technique: diffusion tensor image analysis along the perivascular space (DTI-ALPS) in Alzheimer’s disease cases. Japanese J Radiol 35(4):172–178. https://doi.org/10.1007/s11604-017-0617-z
Boutinaud P, Tsuchida A, Laurent A, Adonias F, Hanifehlou Z, Nozais V et al (2021) 3D Segmentation of Perivascular Spaces on T1-Weighted 3 Tesla MR Images With a Convolutional Autoencoder and a U-Shaped Neural Network. Front Neuroinformatics 15. https://doi.org/10.3389/fninf.2021.641600
Fischl BSD, Busa E et al (2002) Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain. Neuron 33(3):341–355. https://doi.org/10.1016/S0896-6273(02)00569-X
Article CAS PubMed Google Scholar
Tadayon E, Moret B, Sprugnoli G, Monti L, Pascual-Leone A, Santarnecchi E et al (2020) Improving Choroid Plexus Segmentation in the Healthy and Diseased Brain: Relevance for Tau-PET Imaging in Dementia. J Alzheimers Dis 74(4):1057–1068. https://doi.org/10.3233/JAD-190706
Article PubMed PubMed Central Google Scholar
Wu Q, Chen J, Yang X, Zhang X, He W, Xia J (2025) Associations of ventriculomegaly and white matter hyperintensities with glymphatic dysfunction in idiopathic normal pressure hydrocephalus. Eur Radiol. https://doi.org/10.1007/s00330-024-11320-3
Article PubMed PubMed Central Google Scholar
Eide PK, Valnes LM, Pripp AH, Mardal K-A, Ringstad G (2019) Delayed clearance of cerebrospinal fluid tracer from choroid plexus in idiopathic normal pressure hydrocephalus. J Cereb Blood Flow Metabolism 40(9):1849–1858. https://doi.org/10.1177/0271678x19874790
Moses J, Sinclair B, Law M, O’Brien TJ, Vivash L (2022) Automated Methods for Detecting and Quantitation of Enlarged Perivascular spaces on MRI. J Magn Reson Imaging 57(1):11–24. https://doi.org/10.1002/jmri.28369
Article PubMed PubMed Central Google Scholar
Naganawa S, Nakane T, Kawai H, Taoka T (2018) Differences in Signal Intensity and Enhancement on MR Images of the Perivascular Spaces in the Basal Ganglia versus Those in White Matter. Magn Reson Med Sci 17(4):301–307. https://doi.org/10.2463/mrms.mp.2017-0137
Article CAS PubMed PubMed Central Google Scholar
Silverberg GD, Mayo M, Saul T, Rubenstein E, McGuire D (2003) Alzheimer’s disease, normal-pressure hydrocephalus, and senescent changes in CSF circulatory physiology: a hypothesis. Lancet Neurol 2(8):506–511. https://doi.org/10.1016/s1474-4422(03)00487-3
Venkat P, Chopp M, Zacharek A, Cui C, Zhang L, Li Q et al (2017) White matter damage and glymphatic dysfunction in a model of vascular dementia in rats with no prior vascular pathologies. Neurobiol Aging 50:96–106. https://doi.org/10.1016/j.neurobiolaging.2016.11.002
Hasan-Olive MM, Enger R, Hansson HA, Nagelhus EA, Eide PK (2018) Loss of perivascular aquaporin‐4 in idiopathic normal pressure hydrocephalus. Glia 67(1):91–100. https://doi.org/10.1002/glia.23528
Park YW, Shin NY, Chung SJ, Kim J, Lim SM, Lee PH et al (2019) Magnetic Resonance Imaging–Visible Perivascular Spaces in Basal Ganglia Predict Cognitive Decline in Parkinson’s Disease. Mov Disord 34(11):1672–1679. https://doi.org/10.1002/mds.27798
Vinje V, Eklund A, Mardal K-A, Rognes ME, Støverud K-H (2020) Intracranial pressure elevation alters CSF clearance pathways. Fluids Barriers CNS 17(1). https://doi.org/10.1186/s12987-020-00189-1
Liu G, Mestre H, Sweeney AM, Sun Q, Weikop P, Du T et al (2020) Direct Measurement of Cerebrospinal Fluid Production in Mice. Cell Rep 33(12). https://doi.org/10.1016/j.celrep.2020.108524
Liu R, Zhang Z, Chen Y, Liao J, Wang Y, Liu J et al (2022) Choroid plexus epithelium and its role in neurological diseases. Front Mol Neurosci 15. https://doi.org/10.3389/fnmol.2022.949231
Maller VV, Gray RI (2016) Noncommunicating Hydrocephalus. Seminars in Ultrasound. CT MRI 37(2):109–119. https://doi.org/10.1053/j.sult.2015.12.004
Park C, Shin NY, Nam Y, Yoon U, Ahn K, Lee SK (2023) Characteristics of perivascular space dilatation in normal aging. Hum Brain Mapp 44(8):3232–3240. https://doi.org/10.1002/hbm.26277
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