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Posterior integration and thalamo-frontotemporal broadcasting are impaired in disorders of consciousness

Panda, R.; Lopez-Gonzalez, A.; Gilson, M.; Gosseries, O.; Thibaut, A.; Frasso, G.; Cecconi, B.; Escrichs, A.; GIGA group collaborators, ; Deco, G.; Laureys, S.; Zamora-Lopez, G.; Annen, J.

2021-11-10 neuroscience
10.1101/2021.11.08.467694 bioRxiv
Show abstract

The study of the brains static and dynamical activity is opening a valuable source of assistance for the clinical assessment of patients with disorders of consciousness. For example, glucose uptake and dysfunctional spread of naturalistic and synthetic stimuli has proven useful to characterize hampered consciousness. However, understanding of the mechanisms behind loss of consciousness following brain injury is still missing. Here, we study the propagation of endogenous and in-silico exogenous perturbations in patients with disorders of consciousness, based upon directed and causal interactions estimated from resting-state fMRI. We found that patients with disorders of consciousness suffer decreased capacity for neural propagation and responsiveness to events, and that this can be related to glucose metabolism as measured with [18F]FDG-PET. In particular, we show that loss of consciousness is related to the malfunctioning of two neural circuits: the posterior cortical regions failing to convey information, in conjunction with reduced broadcasting of information from subcortical, temporal, parietal and frontal regions. These results seed light on the mechanisms behind disorders of consciousness, triangulating network function with basic measures of brain integrity and behavior. HighlightsO_LIPropagation of neural events and network responses are disrupted in patients with DoC. C_LIO_LILoss of consciousness is related to the malfunctioning of two neural circuits. C_LIO_LIPosterior cortical regions lack to integrate information in altered consciousness. C_LIO_LIBreakdown of information broadcasting of subcortical cortical areas in DoC. C_LIO_LILoss of network responses in DoC patients is related to glucose metabolism. C_LI

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