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 in | Journal of neuropathology and experimental neurology Vol. 76; no. 12; pp. 1034 - 1045 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.12.2017
by American Association of Neuropathologists, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0022-3069 1554-6578 1554-6578 |
DOI | 10.1093/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. |
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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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Keywords | Brain water turnover Human brain biopsy Capillary basement membrane thickness Neurovascular unit Pericyte degeneration Pericyte coverage |
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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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