4.4 Article

Metabolic Brain Covariant Networks as Revealed by FDG-PET with Reference to Resting-State fMRI Networks

期刊

BRAIN CONNECTIVITY
卷 2, 期 5, 页码 275-283

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/brain.2012.0086

关键词

brain metabolism; brain network; default-mode network; independent component analysis; metabolism covariance; PET

资金

  1. National Institute of Health [5R01AG032088]
  2. Alzheimer's Disease Neuroimaging Initiative (ADNI
  3. National Institutes of Health) [U01 AG024904]
  4. NIA
  5. NIBIB
  6. Abbott
  7. Alzheimer's Association
  8. Alzheimer's Drug Discovery Foundation
  9. Amorfix Life Sciences Ltd.
  10. AstraZeneca
  11. Bayer HealthCare
  12. BioClinica, Inc.
  13. Biogen Idec, Inc.
  14. Bristol-Myers Squibb Company
  15. Eisai, Inc.
  16. Elan Pharmaceuticals, Inc.
  17. Eli Lilly and Company
  18. F. Hoffmann-La Roche Ltd.
  19. Genentech, Inc.
  20. GE Healthcare
  21. Innogenetics, N.V.
  22. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  23. Johnson & Johnson Pharmaceutical Research & Development LLC.
  24. Medpace, Inc.
  25. Merck Co., Inc.
  26. Meso Scale Diagnostics, LLC.
  27. Novartis Pharmaceuticals Corporation
  28. Pfizer, Inc.
  29. Servier
  30. Synarc, Inc.
  31. Takeda Pharmaceutical Company
  32. Canadian Institutes of Health Research
  33. NIH [P30 AG010129, K01 AG030514]
  34. Dana Foundation

向作者/读者索取更多资源

The human brain is inherently organized as separate networks, as has been widely revealed by resting-state functional magnetic resonance imaging (fMRI). Although the large-scale functional connectivity can be partially explained by the underlying white-matter structural connectivity, the question of whether the underlying functional connectivity is related to brain metabolic factors is still largely unanswered. The present study investigated the presence of metabolic covariant networks across subjects using a set of fluorodeoxyglucose (F-18, FDG) positron-emission tomography (PET) images. Spatial-independent component analysis was performed on the subject series of FDG-PET images. A number of networks that were mainly homotopic regions could be identified, including visual, auditory, motor, cerebellar, and subcortical networks. However, the anterior-posterior networks such as the default-mode and left frontoparietal networks could not be observed. Region-of-interest-based correlation analysis confirmed that the intersubject metabolic covariances within the default-mode and left frontoparietal networks were reduced as compared with corresponding time-series correlations using resting-state fMRI from an independent sample. In contrast, homotopic intersubject metabolic covariances observed using PET were comparable to the corresponding fMRI resting-state time-series correlations. The current study provides preliminary illustration, suggesting that the human brain metabolism pertains to organized covariance patterns that might partially reflect functional connectivity as revealed by resting-state blood oxygen level dependent (BOLD). The discrepancy between the PET covariance and BOLD functional connectivity might reflect the differences of energy consumption coupling and ongoing neural synchronization within these brain networks.

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