The site of the Media Sphera Publishers contains materials intended solely for healthcare professionals.
By closing this message, you confirm that you are a certified medical professional or a student of a medical educational institution.

Gavrilov G.V.

Kirov Military Medical Academy, St.-Petersburg, Russia

Stanishevskiy A.V.

Military medical Academy named after S. M. Kirov, Saint-Petersburg, Russia

Gaydar B.V.

Kirov Military Medical Academy, St.-Petersburg, Russia

Paramonova N.M.

Kirov Military Medical Academy, St.-Petersburg, Russia;
Sechenov Institute of Evolutionary Physiology and Biochemistry, St.-Petersburg, Russia

Gaykova O.N.

Institute of Toxicology, St.-Petersburg, Russia

Svistov D.V.

Voenno-meditsinskaia akademiia im. S.M. Kirova, Sankt-Peterburg

Pathological changes in human brain biopsies from patients with idiopathic normal pressure hydrocephalus

Authors:

Gavrilov G.V., Stanishevskiy A.V., Gaydar B.V., Paramonova N.M., Gaykova O.N., Svistov D.V.

More about the authors

Read: 3074 times


To cite this article:

Gavrilov GV, Stanishevskiy AV, Gaydar BV, Paramonova NM, Gaykova ON, Svistov DV. Pathological changes in human brain biopsies from patients with idiopathic normal pressure hydrocephalus. S.S. Korsakov Journal of Neurology and Psychiatry. 2019;119(3):50‑54. (In Russ.)
https://doi.org/10.17116/jnevro201911903150

Recommended articles:
Cognitive impairment in patients with Parkinson’s disease. S.S. Korsakov Journal of Neurology and Psychiatry. 2024;(11):81-90
Modern view on the etiology of gallstone disease in children. Russian Journal of Evidence-Based Gastroenterology. 2024;(4):59-68
Black Acanthosis: Diagnosis and Treatment Issues. Russian Journal of Clinical Dermatology and Vene­reology. 2024;(6):709-712
Ultrastructural changes of skeletal muscle tissue of patients with dysferlinopathy. Russian Journal of Archive of Pathology. 2025;(1):28-36
Liver pathology in COVID-19. Russian Journal of Archive of Pathology. 2025;(1):53-59
Infe­ctious factors in atopic dermatitis, pharmaceutical possibilities (systematic lite­rature review). Russian Journal of Clinical Dermatology and Vene­reology. 2025;(1):7-15
Epidemiology of M. geni­talium infe­ction. What is known?. Russian Journal of Clinical Dermatology and Vene­reology. 2025;(2):143-152

References:

  1. Jaraj D, Rabiei K, Marlow T, Jensen C, Skoog I, Wikkelsø C. Prevalence of idiopathic normal-pressure hydrocephalus. Neurology. 2014;82:1449-1454. https://doi.org/10.1212/WNL.0000000000000342
  2. Mori E, Ishikawa M, Kato T, Kazui H, Miyake H, Miyajima M, Nakajima M, Hashimoto M, Kuriyama N, Tokuda T, Ishii K, Kaijima M, Hirata Y, Saito M, Arai H. Guidelines for management of idiopathic normal pressure hydrocephalus: second edition. Neurol Med Chir (Tokyo). 2012;52:775-809.
  3. Kehler U. Normal pressure hydrocephalus: is it worthwhile to treat bedridden patients? Fluids and Barriers of the CNS. 2017;14:17-22.
  4. Khani M, Sass LR, Xing T, Sharp KM, Balédent O, Martin BA. Anthropomorphic Model of Intrathecal Cerebrospinal Fluid Dynamics Within the Spinal Subarachnoid Space: Spinal Cord Nerve Roots Increase Steady-Streaming. J Biomech Eng. 2018;140:39-44. https://doi.org/10.1115/1.4040401
  5. Asgari S, Vespa PM, Bergsneider M, Hu X. Latency relationships between cerebral blood flow velocity and intracranial pressure. Acta Neurochir. 2012;114:5-9. https://doi.org/10.1007/978-3-7091-0956-4_2
  6. Asgari M, Zelicourt D, Kurtcuoglu V. Does glymphatic solute transport need paravascular bulk flow? Fluids and Barriers of the CNS. 2017;14:17-23.
  7. Ringstad G, Valnes LM, Dale AM, Pripp AH, Vatnehol SS, Emblem KE, Mardal KA, Eide PK. Brain-wide glymphatic enhancement and clearance in humans assessed with MRI. JCI Insight. 2018;13. Epub ahead of print. https://doi.org/10.1172/jci.insight.121537
  8. Owler BK, Pena A, Momjian S, Czosnyka Z, Czosnyka M, Harris NG, Smielewski P, Fryer T, Donvan T, Carpenter A, Pickard JD. Changes in cerebral blood flow during cerebrospinal fluid pressure manipulation in patients with normal pressure hydrocephalus: a methodological study. J Cereb Blood Flow Metab. 2004;24:579-587.
  9. Bradley WG. Cerebrospinal fluid dynamics and shunt responsiveness in patients with normal-pressure hydrocephalus. Mayo Clin Proc. 2002;77:507-508.
  10. Bateman GA, Levi CR, Schofield P, Wang Y, Lovett EC. The venous manifestations of pulse wave encephalopathy: windkessel dysfunction in normal aging and senile dementia. Neuroradiology. 2008;50:491-497. Epub 2008 Apr 1. https://doi.org/10.1007/s00234-008-0374-x
  11. Hattingen E, Jurcoane A, Melber J, Blasel S, Zanella FE, Neumann-Haefelin T, Singer OC. Diffusion tensor imaging in patients with adult chronic idiopathic hydrocephalus. Neurosurgery. 2010;66:917-924. https://doi.org/10.1227/01.NEU.0000367801.35654.EC
  12. Radovnický T, Adámek D, Derner M, Sameš M. Fractional anisotropy in patients with disproportionately enlarged subarachnoid space hydrocephalus. Acta Neurochir (Wien). 2016;158:1495-1500. https://doi.org/10.1007/s00701-016-2861-x
  13. Kang K, Yoon U, Choi W, Lee HW. Diffusion tensor imaging of idiopathic normal-pressure hydrocephalus and the cerebrospinal fluid tap test. J Neurol Sci. 2016;364:90-96. https://doi.org/10.1016/j.jns.2016.02.067
  14. Kamiya K, Hori M, Irie R, Miyajima M, Nakajima M, Kamagata K, Tsuruta K, Saito A, Nakazawa M, Suzuki Y, Mori H, Kunimatsu A, Arai H, Aoki S, Abe O. Diffusion imaging of reversible and irreversible microstructural changes within the corticospinal tract in idiopathic normal pressure hydrocephalus. Neuroimage Clin. 2017;14:663-671. eCollection 2017. https://doi.org/10.1016/j.nicl.2017.03.003
  15. Kanno S, Saito M, Kashinoura T, Nishio Y, Iizuka O, Kikuchi H, Takagi M, Iwasaki M, Takahashi S, Mori E. A change in brain white matter after shunt surgery in idiopathic normal pressure hydrocephalus: a tract-based spatial statistics study. Fluids Barriers CNS. 2017;14:32-36. https://doi.org/10.1186/s12987-016-0048-8
  16. Di Rocco C, Pettorossi VE, Caldarelli M, Mancinelli R, Velardi F. Communicating hydrocephalus induced by mechanically increased amplitude of the intraventricular cerebrospinal fluid pressure: Experimental studies. Exp Neurol. 1978;59:40-52.
  17. Ringstad G, Valnes LM, Dale AM, Pripp AH, Vatnehol SS, Emblem KE, Mardal KA, Eide PK. Brain-wide glymphatic enhancement and clearance in humans assessed with MRI. JCI Insight. 2018;13. Epub ahead of print. https://doi.org/10.1172/jci.insight.121537.
  18. Cabral D, Beach TG, Vedders L, Sue LI, Jacobson S, Myers K, Sabbagh MN. Frequency of Alzheimer’s disease pathology at autopsy in patients with clinical normal pressure hydrocephalus. Alzheimers Dement. 2011;7:509-513. https://doi.org/10.1016/j.jalz.2010.12.008

Email Confirmation

An email was sent to test@gmail.com with a confirmation link. Follow the link from the letter to complete the registration on the site.

Email Confirmation

We use cооkies to improve the performance of the site. By staying on our site, you agree to the terms of use of cооkies. To view our Privacy and Cookie Policy, please. click here.