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Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old
INTRODUCTION: Age-related vascular changes, including blood pressure elevation and cerebral blood flow (CBF) reduction, are associated with cognitive decline and Alzheimer’s disease (AD). Evidence suggests that the relationship between blood pressure and dementia risk varies between younger and olde...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942967/ https://www.ncbi.nlm.nih.gov/pubmed/27391477 http://dx.doi.org/10.1186/s13195-014-0080-3 |
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author | Clark, Lindsay R Nation, Daniel A Wierenga, Christina E Bangen, Katherine J Dev, Sheena I Shin, David D Delano-Wood, Lisa Liu, Thomas T Rissman, Robert A Bondi, Mark W |
author_facet | Clark, Lindsay R Nation, Daniel A Wierenga, Christina E Bangen, Katherine J Dev, Sheena I Shin, David D Delano-Wood, Lisa Liu, Thomas T Rissman, Robert A Bondi, Mark W |
author_sort | Clark, Lindsay R |
collection | PubMed |
description | INTRODUCTION: Age-related vascular changes, including blood pressure elevation and cerebral blood flow (CBF) reduction, are associated with cognitive decline and Alzheimer’s disease (AD). Evidence suggests that the relationship between blood pressure and dementia risk varies between younger and older samples within the elderly population. METHODS: We examined the relationship between mean arterial pressure (MAP), CBF, and cognition in young-old (60 to 75 years of age) versus very-old (80+ years of age) adults. Fifty-eight non-demented older adults completed an arterial spin labeling MRI scan, and an index of cerebrovascular resistance (CVRi) was estimated for each participant by calculating the ratio of MAP and CBF. RESULTS: Results demonstrated a similar negative relationship between MAP and CBF across both age groups. However, very-old participants exhibited elevated CVRi and reduced CBF compared to young-old participants in regions implicated in AD and cerebral small vessel disease. Furthermore, significant age by CVRi interactions revealed that elevated CVRi in the thalamus was inversely related to verbal fluency performance in the very-old group. CONCLUSIONS: Findings support CVRi as a potential vascular biomarker and suggest that regionally-specific vascular changes may contribute to cognitive decline, particularly in the very-old. |
format | Online Article Text |
id | pubmed-4942967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49429672016-07-14 Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old Clark, Lindsay R Nation, Daniel A Wierenga, Christina E Bangen, Katherine J Dev, Sheena I Shin, David D Delano-Wood, Lisa Liu, Thomas T Rissman, Robert A Bondi, Mark W Alzheimers Res Ther Research INTRODUCTION: Age-related vascular changes, including blood pressure elevation and cerebral blood flow (CBF) reduction, are associated with cognitive decline and Alzheimer’s disease (AD). Evidence suggests that the relationship between blood pressure and dementia risk varies between younger and older samples within the elderly population. METHODS: We examined the relationship between mean arterial pressure (MAP), CBF, and cognition in young-old (60 to 75 years of age) versus very-old (80+ years of age) adults. Fifty-eight non-demented older adults completed an arterial spin labeling MRI scan, and an index of cerebrovascular resistance (CVRi) was estimated for each participant by calculating the ratio of MAP and CBF. RESULTS: Results demonstrated a similar negative relationship between MAP and CBF across both age groups. However, very-old participants exhibited elevated CVRi and reduced CBF compared to young-old participants in regions implicated in AD and cerebral small vessel disease. Furthermore, significant age by CVRi interactions revealed that elevated CVRi in the thalamus was inversely related to verbal fluency performance in the very-old group. CONCLUSIONS: Findings support CVRi as a potential vascular biomarker and suggest that regionally-specific vascular changes may contribute to cognitive decline, particularly in the very-old. BioMed Central 2015-01-21 /pmc/articles/PMC4942967/ /pubmed/27391477 http://dx.doi.org/10.1186/s13195-014-0080-3 Text en © Clark et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Clark, Lindsay R Nation, Daniel A Wierenga, Christina E Bangen, Katherine J Dev, Sheena I Shin, David D Delano-Wood, Lisa Liu, Thomas T Rissman, Robert A Bondi, Mark W Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
title | Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
title_full | Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
title_fullStr | Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
title_full_unstemmed | Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
title_short | Elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
title_sort | elevated cerebrovascular resistance index is associated with cognitive dysfunction in the very-old |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942967/ https://www.ncbi.nlm.nih.gov/pubmed/27391477 http://dx.doi.org/10.1186/s13195-014-0080-3 |
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