Brain Capillary Ultrastructure in Idiopathic Normal Pressure Hydrocephalus: Relationship With Static and Pulsatile Intracranial Pressure

Abstract Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was...

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Published inJournal of neuropathology and experimental neurology Vol. 76; no. 12; pp. 1034 - 1045
Main Authors Eidsvaag, Vigdis Andersen, Hansson, Hans-Arne, Heuser, Kjell, Nagelhus, Erlend A., Eide, Per K.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.12.2017
by American Association of Neuropathologists, Inc
Subjects
Online AccessGet full text
ISSN0022-3069
1554-6578
1554-6578
DOI10.1093/jnen/nlx091

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Abstract Abstract Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
AbstractList Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9x10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
Abstract Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
Abstract Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal cortex biopsies from iNPH patients and related the observations to overnight intracranial pressure (ICP) scores. A biopsy (0.9×10 mm) was taken from where the ICP sensor subsequently was inserted. Brain capillaries were investigated by electron microscopy of biopsies from 27 iNPH patients and 10 reference subjects, i.e. patients (not healthy individuals) without cerebrospinal fluid circulation disturbances, in whom normal brain tissue was removed as part of necessary neurosurgical treatment. Degenerating and degenerated pericyte processes were identified in 23/27 (85%) iNPH and 6/10 (60%) of reference specimens. Extensive disintegration of pericyte processes were recognized in 11/27 (41%) iNPH and 1/10 (10%) reference specimens. There were no differences in basement membrane (BM) thickness or pericyte coverage between iNPH and reference subjects. The pulsatile or static ICP scores did neither correlate with the BM thickness nor with pericyte coverage. We found increased prevalence of degenerating pericytes in iNPH while the BM thickness and pericyte coverage did not differ from the reference individuals. Observations in iNPH may to some extent be age-related since the iNPH patients were significantly older than the reference individuals.
Author Nagelhus, Erlend A.
Heuser, Kjell
Hansson, Hans-Arne
Eidsvaag, Vigdis Andersen
Eide, Per K.
AuthorAffiliation From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
AuthorAffiliation_xml – name: From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
Author_xml – sequence: 1
  givenname: Vigdis Andersen
  surname: Eidsvaag
  fullname: Eidsvaag, Vigdis Andersen
  organization: From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
– sequence: 2
  givenname: Hans-Arne
  surname: Hansson
  fullname: Hansson, Hans-Arne
  organization: From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
– sequence: 3
  givenname: Kjell
  surname: Heuser
  fullname: Heuser, Kjell
  organization: From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
– sequence: 4
  givenname: Erlend A.
  surname: Nagelhus
  fullname: Nagelhus, Erlend A.
  organization: From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
– sequence: 5
  givenname: Per K.
  surname: Eide
  fullname: Eide, Per K.
  email: p.k.eide@medisin.uio.no
  organization: From the Department of Neurosurgery, Oslo University Hospital – Rikshospitalet, Oslo, Norway (VAE, PKE); Faculty of Medicine (VAE, EAN, PKE); and Division of Physiology, Department of Molecular Medicine, GliaLab and Letten Centre, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway (VAE, EAN); Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden (H-AH); and Department of Neurology, Oslo University Hospital – Rikshospitalet, Oslo, Norway (KH, EAN)
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ContentType Journal Article
Copyright 2017 American Association of Neuropathologists, Inc. All rights reserved. 2017
2017 by American Association of Neuropathologists, Inc.
2017 American Association of Neuropathologists, Inc. All rights reserved.
Copyright © 2017 American Association of Neuropathologists
Copyright_xml – notice: 2017 American Association of Neuropathologists, Inc. All rights reserved. 2017
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Issue 12
Keywords Brain water turnover
Human brain biopsy
Capillary basement membrane thickness
Neurovascular unit
Pericyte degeneration
Pericyte coverage
Language English
License 2017 American Association of Neuropathologists, Inc. All rights reserved.
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Snippet Abstract Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in...
Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in frontal...
Abstract Idiopathic normal pressure hydrocephalus (iNPH) is a neurodegenerative disease of unknown cause. We investigated the morphology of capillaries in...
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SubjectTerms Adult
Age Factors
Aged
Aged, 80 and over
alzheimers-disease
aquaporin-4 polarization
arterioles
basement-membrane
Biopsy
Brain - blood supply
Brain - diagnostic imaging
Brain - ultrastructure
Brain water turnover
Capillaries - diagnostic imaging
Capillaries - ultrastructure
Capillary basement membrane thickness
Cell and Molecular Biology
Cell- och molekylärbiologi
cerebral-blood-flow
Cohort Studies
drainage
features
Female
Human brain biopsy
Humans
Hydrocephalus, Normal Pressure - diagnostic imaging
Hydrocephalus, Normal Pressure - physiopathology
Intracranial Pressure - physiology
Male
microvessels
Middle Aged
mouse cortical astrocytes
Neurosciences
Neurosciences & Neurology
Neurovascular
Neurovetenskaper
Pathology
pericyte degeneration
Prospective Studies
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Title Brain Capillary Ultrastructure in Idiopathic Normal Pressure Hydrocephalus: Relationship With Static and Pulsatile Intracranial Pressure
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