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Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease
BACKGROUND: Abnormalities in cerebrospinal fluid (CSF) production and turnover, seen in normal pressure hydrocephalus (NPH) and in Alzheimer's disease (AD), may be an important cause of amyloid retention in the brain and may relate the two diseases. There is a high incidence of AD pathology in...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538629/ https://www.ncbi.nlm.nih.gov/pubmed/16737542 http://dx.doi.org/10.1186/1743-8454-3-7 |
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author | Silverberg, Gerald Mayo, Martha Saul, Thomas Fellmann, Jere McGuire, Dawn |
author_facet | Silverberg, Gerald Mayo, Martha Saul, Thomas Fellmann, Jere McGuire, Dawn |
author_sort | Silverberg, Gerald |
collection | PubMed |
description | BACKGROUND: Abnormalities in cerebrospinal fluid (CSF) production and turnover, seen in normal pressure hydrocephalus (NPH) and in Alzheimer's disease (AD), may be an important cause of amyloid retention in the brain and may relate the two diseases. There is a high incidence of AD pathology in patients being shunted for NPH, the AD-NPH syndrome. We now report elevated CSF pressure (CSFP), consistent with very early hydrocephalus, in a subset of AD patients enrolled in a clinical trial of chronic low-flow CSF drainage. Our objective was to determine the frequency of elevated CSFP in subjects meeting National Institutes of Neurological and Communicative Diseases and Stroke – Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria for AD, excluding those with signs of concomitant NPH. METHODS: AD subjects by NINCDS-ADRDA criteria (n = 222), were screened by history, neurological examination, and radiographic imaging to exclude those with clinical or radiographic signs of NPH. As part of this exclusion process, opening CSFP was measured supine under general anesthesia during device implantation surgery at a controlled pCO(2 )of 40 Torr (40 mmHg). RESULTS: Of the 222 AD subjects 181 had pressure measurements recorded. Seven subjects (3.9%) enrolled in the study had CSFP of 220 mmH(2)0 or greater, mean 249 ± 20 mmH(2)0 which was significantly higher than 103 ± 47 mmH(2)O for the AD-only group. AD-NPH patients were significantly younger and significantly less demented on the Mattis Dementia Rating Scale (MDRS). CONCLUSION: Of the AD subjects who were carefully screened to exclude those with clinical NPH, 4% had elevated CSFP. These subjects were presumed to have the AD-NPH syndrome and were withdrawn from the remainder of the study. |
format | Text |
id | pubmed-1538629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15386292006-08-10 Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease Silverberg, Gerald Mayo, Martha Saul, Thomas Fellmann, Jere McGuire, Dawn Cerebrospinal Fluid Res Research BACKGROUND: Abnormalities in cerebrospinal fluid (CSF) production and turnover, seen in normal pressure hydrocephalus (NPH) and in Alzheimer's disease (AD), may be an important cause of amyloid retention in the brain and may relate the two diseases. There is a high incidence of AD pathology in patients being shunted for NPH, the AD-NPH syndrome. We now report elevated CSF pressure (CSFP), consistent with very early hydrocephalus, in a subset of AD patients enrolled in a clinical trial of chronic low-flow CSF drainage. Our objective was to determine the frequency of elevated CSFP in subjects meeting National Institutes of Neurological and Communicative Diseases and Stroke – Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria for AD, excluding those with signs of concomitant NPH. METHODS: AD subjects by NINCDS-ADRDA criteria (n = 222), were screened by history, neurological examination, and radiographic imaging to exclude those with clinical or radiographic signs of NPH. As part of this exclusion process, opening CSFP was measured supine under general anesthesia during device implantation surgery at a controlled pCO(2 )of 40 Torr (40 mmHg). RESULTS: Of the 222 AD subjects 181 had pressure measurements recorded. Seven subjects (3.9%) enrolled in the study had CSFP of 220 mmH(2)0 or greater, mean 249 ± 20 mmH(2)0 which was significantly higher than 103 ± 47 mmH(2)O for the AD-only group. AD-NPH patients were significantly younger and significantly less demented on the Mattis Dementia Rating Scale (MDRS). CONCLUSION: Of the AD subjects who were carefully screened to exclude those with clinical NPH, 4% had elevated CSFP. These subjects were presumed to have the AD-NPH syndrome and were withdrawn from the remainder of the study. BioMed Central 2006-05-31 /pmc/articles/PMC1538629/ /pubmed/16737542 http://dx.doi.org/10.1186/1743-8454-3-7 Text en Copyright © 2006 Silverberg et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Silverberg, Gerald Mayo, Martha Saul, Thomas Fellmann, Jere McGuire, Dawn Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease |
title | Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease |
title_full | Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease |
title_fullStr | Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease |
title_full_unstemmed | Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease |
title_short | Elevated cerebrospinal fluid pressure in patients with Alzheimer's disease |
title_sort | elevated cerebrospinal fluid pressure in patients with alzheimer's disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538629/ https://www.ncbi.nlm.nih.gov/pubmed/16737542 http://dx.doi.org/10.1186/1743-8454-3-7 |
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