A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.

Glucose is the predominant fuel supporting brain function. If the brain's entire glucose supply is consumed by oxidative phosphorylation, the molar ratio of oxygen to glucose consumption (OGI) is equal to 6. An OGI of less than 6 is evidence of non-oxidative glucose metabolism. Several studies...

Full description

Bibliographic Details
Main Authors: Tyler Blazey, Abraham Z Snyder, Manu S Goyal, Andrei G Vlassenko, Marcus E Raichle
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0204242
_version_ 1819259591504953344
author Tyler Blazey
Abraham Z Snyder
Manu S Goyal
Andrei G Vlassenko
Marcus E Raichle
author_facet Tyler Blazey
Abraham Z Snyder
Manu S Goyal
Andrei G Vlassenko
Marcus E Raichle
author_sort Tyler Blazey
collection DOAJ
description Glucose is the predominant fuel supporting brain function. If the brain's entire glucose supply is consumed by oxidative phosphorylation, the molar ratio of oxygen to glucose consumption (OGI) is equal to 6. An OGI of less than 6 is evidence of non-oxidative glucose metabolism. Several studies have reported that the OGI in the resting human brain is less than 6.0, but the exact value remains uncertain. Additionally, it is not clear if lactate efflux accounts for the difference between OGI and its theoretical value of 6.0. To address these issues, we conducted a meta-analysis of OGI and oxygen-to-carbohydrate (glucose + 0.5*lactate; OCI) ratios in healthy young and middle-aged adults. We identified 47 studies that measured at least one of these ratios using arterio-venous differences of glucose, lactate, and oxygen. Using a Bayesian random effects model, the population median OGI was 5.46 95% credible interval (5.25-5.66), indicating that approximately 9% of the brain's glucose metabolism is non-oxidative. The population median OCI was 5.60 (5.36-5.84), suggesting that lactate efflux does not account for all non-oxidative glucose consumption. Significant heterogeneity across studies was observed, which implies that further work is needed to characterize how demographic and methodological factors influence measured cerebral metabolic ratios.
first_indexed 2024-12-23T19:12:27Z
format Article
id doaj.art-8e1767395e5b43f1b77aaacb6aac7661
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-23T19:12:27Z
publishDate 2018-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-8e1767395e5b43f1b77aaacb6aac76612022-12-21T17:34:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01139e020424210.1371/journal.pone.0204242A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.Tyler BlazeyAbraham Z SnyderManu S GoyalAndrei G VlassenkoMarcus E RaichleGlucose is the predominant fuel supporting brain function. If the brain's entire glucose supply is consumed by oxidative phosphorylation, the molar ratio of oxygen to glucose consumption (OGI) is equal to 6. An OGI of less than 6 is evidence of non-oxidative glucose metabolism. Several studies have reported that the OGI in the resting human brain is less than 6.0, but the exact value remains uncertain. Additionally, it is not clear if lactate efflux accounts for the difference between OGI and its theoretical value of 6.0. To address these issues, we conducted a meta-analysis of OGI and oxygen-to-carbohydrate (glucose + 0.5*lactate; OCI) ratios in healthy young and middle-aged adults. We identified 47 studies that measured at least one of these ratios using arterio-venous differences of glucose, lactate, and oxygen. Using a Bayesian random effects model, the population median OGI was 5.46 95% credible interval (5.25-5.66), indicating that approximately 9% of the brain's glucose metabolism is non-oxidative. The population median OCI was 5.60 (5.36-5.84), suggesting that lactate efflux does not account for all non-oxidative glucose consumption. Significant heterogeneity across studies was observed, which implies that further work is needed to characterize how demographic and methodological factors influence measured cerebral metabolic ratios.https://doi.org/10.1371/journal.pone.0204242
spellingShingle Tyler Blazey
Abraham Z Snyder
Manu S Goyal
Andrei G Vlassenko
Marcus E Raichle
A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.
PLoS ONE
title A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.
title_full A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.
title_fullStr A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.
title_full_unstemmed A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.
title_short A systematic meta-analysis of oxygen-to-glucose and oxygen-to-carbohydrate ratios in the resting human brain.
title_sort systematic meta analysis of oxygen to glucose and oxygen to carbohydrate ratios in the resting human brain
url https://doi.org/10.1371/journal.pone.0204242
work_keys_str_mv AT tylerblazey asystematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT abrahamzsnyder asystematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT manusgoyal asystematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT andreigvlassenko asystematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT marcuseraichle asystematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT tylerblazey systematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT abrahamzsnyder systematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT manusgoyal systematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT andreigvlassenko systematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain
AT marcuseraichle systematicmetaanalysisofoxygentoglucoseandoxygentocarbohydrateratiosintherestinghumanbrain