Cargando…
Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain
The correspondence between cerebral glucose metabolism (indexing energy utilization) and synchronous fluctuations in blood oxygenation (indexing neuronal activity) is relevant for neuronal specialization and is affected by brain disorders. Here, we define novel measures of relative power (rPWR, exte...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370887/ https://www.ncbi.nlm.nih.gov/pubmed/30741935 http://dx.doi.org/10.1038/s41467-019-08546-x |
_version_ | 1783394450176737280 |
---|---|
author | Shokri-Kojori, Ehsan Tomasi, Dardo Alipanahi, Babak Wiers, Corinde E. Wang, Gene-Jack Volkow, Nora D. |
author_facet | Shokri-Kojori, Ehsan Tomasi, Dardo Alipanahi, Babak Wiers, Corinde E. Wang, Gene-Jack Volkow, Nora D. |
author_sort | Shokri-Kojori, Ehsan |
collection | PubMed |
description | The correspondence between cerebral glucose metabolism (indexing energy utilization) and synchronous fluctuations in blood oxygenation (indexing neuronal activity) is relevant for neuronal specialization and is affected by brain disorders. Here, we define novel measures of relative power (rPWR, extent of concurrent energy utilization and activity) and relative cost (rCST, extent that energy utilization exceeds activity), derived from FDG-PET and fMRI. We show that resting-state networks have distinct energetic signatures and that brain could be classified into major bilateral segments based on rPWR and rCST. While medial-visual and default-mode networks have the highest rPWR, frontoparietal networks have the highest rCST. rPWR and rCST estimates are generalizable to other indexes of energy supply and neuronal activity, and are sensitive to neurocognitive effects of acute and chronic alcohol exposure. rPWR and rCST are informative metrics for characterizing brain pathology and alternative energy use, and may provide new multimodal biomarkers of neuropsychiatric disorders. |
format | Online Article Text |
id | pubmed-6370887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63708872019-02-13 Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain Shokri-Kojori, Ehsan Tomasi, Dardo Alipanahi, Babak Wiers, Corinde E. Wang, Gene-Jack Volkow, Nora D. Nat Commun Article The correspondence between cerebral glucose metabolism (indexing energy utilization) and synchronous fluctuations in blood oxygenation (indexing neuronal activity) is relevant for neuronal specialization and is affected by brain disorders. Here, we define novel measures of relative power (rPWR, extent of concurrent energy utilization and activity) and relative cost (rCST, extent that energy utilization exceeds activity), derived from FDG-PET and fMRI. We show that resting-state networks have distinct energetic signatures and that brain could be classified into major bilateral segments based on rPWR and rCST. While medial-visual and default-mode networks have the highest rPWR, frontoparietal networks have the highest rCST. rPWR and rCST estimates are generalizable to other indexes of energy supply and neuronal activity, and are sensitive to neurocognitive effects of acute and chronic alcohol exposure. rPWR and rCST are informative metrics for characterizing brain pathology and alternative energy use, and may provide new multimodal biomarkers of neuropsychiatric disorders. Nature Publishing Group UK 2019-02-11 /pmc/articles/PMC6370887/ /pubmed/30741935 http://dx.doi.org/10.1038/s41467-019-08546-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shokri-Kojori, Ehsan Tomasi, Dardo Alipanahi, Babak Wiers, Corinde E. Wang, Gene-Jack Volkow, Nora D. Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain |
title | Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain |
title_full | Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain |
title_fullStr | Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain |
title_full_unstemmed | Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain |
title_short | Correspondence between cerebral glucose metabolism and BOLD reveals relative power and cost in human brain |
title_sort | correspondence between cerebral glucose metabolism and bold reveals relative power and cost in human brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370887/ https://www.ncbi.nlm.nih.gov/pubmed/30741935 http://dx.doi.org/10.1038/s41467-019-08546-x |
work_keys_str_mv | AT shokrikojoriehsan correspondencebetweencerebralglucosemetabolismandboldrevealsrelativepowerandcostinhumanbrain AT tomasidardo correspondencebetweencerebralglucosemetabolismandboldrevealsrelativepowerandcostinhumanbrain AT alipanahibabak correspondencebetweencerebralglucosemetabolismandboldrevealsrelativepowerandcostinhumanbrain AT wierscorindee correspondencebetweencerebralglucosemetabolismandboldrevealsrelativepowerandcostinhumanbrain AT wanggenejack correspondencebetweencerebralglucosemetabolismandboldrevealsrelativepowerandcostinhumanbrain AT volkownorad correspondencebetweencerebralglucosemetabolismandboldrevealsrelativepowerandcostinhumanbrain |