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Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects

BACKGROUND AND PURPOSE: Both cerebral hypoperfusion and vascular risk factors have been implicated in early aging of the brain and the development of neurodegenerative disease. However, the current knowledge of the importance of cardiovascular health on resting brain perfusion is limited. The aim of...

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Autores principales: Henriksen, Otto M., Jensen, Lars T., Krabbe, Katja, Guldberg, Per, Teerlink, Tom, Rostrup, Egill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026139/
https://www.ncbi.nlm.nih.gov/pubmed/24840730
http://dx.doi.org/10.1371/journal.pone.0097363
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author Henriksen, Otto M.
Jensen, Lars T.
Krabbe, Katja
Guldberg, Per
Teerlink, Tom
Rostrup, Egill
author_facet Henriksen, Otto M.
Jensen, Lars T.
Krabbe, Katja
Guldberg, Per
Teerlink, Tom
Rostrup, Egill
author_sort Henriksen, Otto M.
collection PubMed
description BACKGROUND AND PURPOSE: Both cerebral hypoperfusion and vascular risk factors have been implicated in early aging of the brain and the development of neurodegenerative disease. However, the current knowledge of the importance of cardiovascular health on resting brain perfusion is limited. The aim of the present study was to elucidate the relation between brain perfusion variability and risk factors of endothelial dysfunction and atherosclerosis in healthy aged subjects. METHODS: Thirty-eight healthy subjects aged 50–75 years old were included. Mean global brain perfusion was measured using magnetic resonance phase contrast mapping and regional brain perfusion by use of arterial spin labeling. RESULTS: Mean global brain perfusion was inversely correlated with caffeine and hematocrit, and positively with end-tidal P(CO2). Furthermore, the mean global brain perfusion was inversely correlated with circulating homocysteine, but not with asymmetric dimethylarginine, dyslipidemia or the carotid intima-media thickness. The relative regional brain perfusion was associated with circulating homocysteine, with a relative parietal hypoperfusion and a frontal hyperperfusion. No effect on regional brain perfusion was observed for any of the other risk factors. A multiple regression model including homocysteine, caffeine, hematocrit and end-tidal P(CO2), explained nearly half of the observed variability. CONCLUSION: Both intrinsic and extrinsic factors influenced global cerebral perfusion variation between subjects. Further, the results suggest that the inverse relation between homocysteine and brain perfusion is owing to other mechanisms, than reflected by asymmetric dimethylarginine, and that homocysteine may be a marker of cerebral perfusion in aging brains.
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spelling pubmed-40261392014-05-21 Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects Henriksen, Otto M. Jensen, Lars T. Krabbe, Katja Guldberg, Per Teerlink, Tom Rostrup, Egill PLoS One Research Article BACKGROUND AND PURPOSE: Both cerebral hypoperfusion and vascular risk factors have been implicated in early aging of the brain and the development of neurodegenerative disease. However, the current knowledge of the importance of cardiovascular health on resting brain perfusion is limited. The aim of the present study was to elucidate the relation between brain perfusion variability and risk factors of endothelial dysfunction and atherosclerosis in healthy aged subjects. METHODS: Thirty-eight healthy subjects aged 50–75 years old were included. Mean global brain perfusion was measured using magnetic resonance phase contrast mapping and regional brain perfusion by use of arterial spin labeling. RESULTS: Mean global brain perfusion was inversely correlated with caffeine and hematocrit, and positively with end-tidal P(CO2). Furthermore, the mean global brain perfusion was inversely correlated with circulating homocysteine, but not with asymmetric dimethylarginine, dyslipidemia or the carotid intima-media thickness. The relative regional brain perfusion was associated with circulating homocysteine, with a relative parietal hypoperfusion and a frontal hyperperfusion. No effect on regional brain perfusion was observed for any of the other risk factors. A multiple regression model including homocysteine, caffeine, hematocrit and end-tidal P(CO2), explained nearly half of the observed variability. CONCLUSION: Both intrinsic and extrinsic factors influenced global cerebral perfusion variation between subjects. Further, the results suggest that the inverse relation between homocysteine and brain perfusion is owing to other mechanisms, than reflected by asymmetric dimethylarginine, and that homocysteine may be a marker of cerebral perfusion in aging brains. Public Library of Science 2014-05-19 /pmc/articles/PMC4026139/ /pubmed/24840730 http://dx.doi.org/10.1371/journal.pone.0097363 Text en © 2014 Henriksen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Henriksen, Otto M.
Jensen, Lars T.
Krabbe, Katja
Guldberg, Per
Teerlink, Tom
Rostrup, Egill
Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects
title Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects
title_full Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects
title_fullStr Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects
title_full_unstemmed Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects
title_short Resting Brain Perfusion and Selected Vascular Risk Factors in Healthy Elderly Subjects
title_sort resting brain perfusion and selected vascular risk factors in healthy elderly subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026139/
https://www.ncbi.nlm.nih.gov/pubmed/24840730
http://dx.doi.org/10.1371/journal.pone.0097363
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