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Brain Energy Metabolism and Blood Flow Differences in Healthy Aging
Author(s) -
Joel Aanerud,
Per Borghammer,
M. Mallar Chakravarty,
Kim Vang,
Anders Rodell,
Kristjana Ýr Jónsdóttir,
Arne Møller,
Mahmoud Ashkanian,
Manouchehr Seyedi Vafaee,
Peter Iversen,
Peter Johannsen,
Albert Gjedde
Publication year - 2012
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.2012.18
Subject(s) - cerebral blood flow , neuroscience , neurodegeneration , somatosensory system , brain aging , positron emission tomography , cerebral cortex , medicine , oxygen metabolism , motor cortex , psychology , oxygen , cognition , chemistry , disease , stimulation , organic chemistry
Cerebral metabolic rate of oxygen consumption ( CMRO 2 ), cerebral blood flow ( CBF), and oxygen extraction fraction ( OEF) are important indices of healthy aging of the brain. Although a frequent topic of study, changes of CBF and CMRO 2 during normal aging are still controversial, as some authors find decreases of both CBF and CMRO 2 but increased OEF, while others find no change, and yet other find divergent changes. In this reanalysis of previously published results from positron emission tomography of healthy volunteers, we determined CMRO 2 and CBF in 66 healthy volunteers aged 21 to 81 years. The magnitudes of CMRO 2 and CBF declined in large parts of the cerebral cortex, including association areas, but the primary motor and sensory areas were relatively spared. We found significant increases of OEF in frontal and parietal cortices, excluding primary motor and somatosensory regions, and in the temporal cortex. Because of the inverse relation between OEF and capillary oxygen tension, increased OEF can compromise oxygen delivery to neurons, with possible perturbation of energy turnover. The results establish a possible mechanism of progression from healthy to unhealthy brain aging, as the regions most affected by age are the areas that are most vulnerable to neurodegeneration.

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