Literature DB >> 28540741

Fine-Grained Parcellation of Brain Connectivity Improves Differentiation of States of Consciousness During Graded Propofol Sedation.

Xiaolin Liu1, Kathryn K Lauer2, B Douglas Ward3, Christopher J Roberts2, Suyan Liu2, Suneeta Gollapudy2, Robert Rohloff4, William Gross2, Zhan Xu3, Guangyu Chen3, Jeffrey R Binder4, Shi-Jiang Li3, Anthony G Hudetz5.   

Abstract

Conscious perception relies on interactions between spatially and functionally distinct modules of the brain at various spatiotemporal scales. These interactions are altered by anesthesia, an intervention that leads to fading consciousness. Relatively little is known about brain functional connectivity and its anesthetic modulation at a fine spatial scale. Here, we used functional imaging to examine propofol-induced changes in functional connectivity in brain networks defined at a fine-grained parcellation based on a combination of anatomical and functional features. Fifteen healthy volunteers underwent resting-state functional imaging in wakeful baseline, mild sedation, deep sedation, and recovery of consciousness. Compared with wakeful baseline, propofol produced widespread, dose-dependent functional connectivity changes that scaled with the extent to which consciousness was altered. The dominant changes in connectivity were associated with the frontal lobes. By examining node pairs that demonstrated a trend of functional connectivity change between wakefulness and deep sedation, quadratic discriminant analysis differentiated the states of consciousness in individual participants more accurately at a fine-grained parcellation (e.g., 2000 nodes) than at a coarse-grained parcellation (e.g., 116 anatomical nodes). Our study suggests that defining brain networks at a high granularity may provide a superior imaging-based distinction of the graded effect of anesthesia on consciousness.

Entities:  

Keywords:  brain parcellation; loss of consciousness; propofol sedation; resting-state fMRI; state classification

Mesh:

Substances:

Year:  2017        PMID: 28540741      PMCID: PMC5685154          DOI: 10.1089/brain.2016.0477

Source DB:  PubMed          Journal:  Brain Connect        ISSN: 2158-0014


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