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Breakdown of within- and between-network Resting State Functional Magnetic Resonance Imaging Connectivity during Propofol-induced Loss of Consciousness
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Background: Mechanisms of anesthesia-induced loss of consciousness remain poorly understood. Resting-state functional magnetic resonance imaging allows investigating whole-brain connectivity changes during pharmacological modulation of the level of consciousness. Methods: Low-frequency spontaneous blood oxygen level-dependent fluctuations were measured in 19 healthy volunteers during wakefulness, mild sedation, deep sedation with clinical unconsciousness, and subsequent recovery of consciousness. Results: Propofol-induced decrease in consciousness linearly correlates with decreased corticocortical and thalamocortical connectivity in frontoparietal networks (i.e., default- and executive-control networks). Furthermore, during propofol-induced unconsciousness, a negative correlation was identified between thalamic and cortical activity in these networks. Finally, negative correlations between default network and lateral frontoparietal cortices activity, present during wakefulness, decreased proportionally to propofol-induced loss of consciousness. In contrast, connectivity was globally preserved in low-level sensory cortices, (i.e., in auditory and visual networks across sedation stages). This was paired with preserved thalamocortical connectivity in these networks. Rather, waning of consciousness was associated with a loss of cross-modal interactions between visual and auditory networks. Conclusions: Our results shed light on the functional significance of spontaneous brain activity fluctuations observed in functional magnetic resonance imaging. They suggest that propofol-induced unconsciousness could be linked to a breakdown of cerebral temporal architecture that modifies both within- and between-network connectivity and thus prevents communication between low-level sensory and higher-order frontoparietal cortices, thought to be necessary for perception of external stimuli. They emphasize the importance of thalamocortical connectivity in higher-order cognitive brain networks in the genesis of conscious perception.
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“Based on fMRI, functional disconnections of frontal-parietal networks have been shown during general anesthesia in humans induced by structurally and pharmacologically diverse agents, including the volatile anesthetic sevoflurane [131, 139–141]”
From The Biology of General Anesthesia from Paramecium to Primate (2019) · cites this paper as [140]
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Cites
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
Self-citationSpontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Neurophysiological investigation of the basis of the fMRI signal
Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,551
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
Self-citationConsistent resting-state networks across healthy subjects
Damoiseaux, J. S., Rombouts, S. A. R. B., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Beckmann, C. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601417103 · Cited by 4,326
Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684
Self-citation(1988) · Cited by 3,656
Investigations into resting-state connectivity using independent component analysis
Beckmann, C. F., DeLuca, M., Devlin, J. T., & Smith, S. M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1634 · Cited by 3,398
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371
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Hutchison, R. M., Womelsdorf, T., Allen, E. A., Bandettini, P. A., Calhoun, V. D., Corbetta, M., Della Penna, S., Duyn, J. H., Glover, G. H., Gonzalez-Castillo, J., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.079 · Cited by 2,962
Conscious Processing and the Global Neuronal Workspace Hypothesis
Mashour, G. A., Roelfsema, P., Changeux, J.-P., & Dehaene, S. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.026 · Cited by 1,164
“29 by fMRI to functionally disconnect prefrontal cortex and posterior parietal cortices (such as the precuneus) in humans (Bonhomme et al., 2016; Boveroux et al., 2010; Palanca et al., 2015).”
BackgroundSignature of consciousness in the dynamics of resting-state brain activity
Barttfeld, P., Uhrig, L., Sitt, J. D., Sigman, M., Jarraya, B., & Dehaene, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418031112 · Cited by 670
Resting-state brain networks: literature review and clinical applications
Rosazza, C., & Minati, L. (2011) · Neurological Sciences · doi:10.1007/s10072-011-0636-y · Cited by 535
Unresponsiveness ≠ unconsciousness
Sanders, R. D., Tononi, G., Laureys, S., Sleigh, J. W., & Warner, D. S. (2012) · Anesthesiology · doi:10.1097/aln.0b013e318249d0a7 · Cited by 474
Self-citationPalhano-Fontes, F., Andrade, K. C., Tofoli, L. F., Santos, A. C., Crippa, J. A. S., Hallak, J. E. C., Ribeiro, S., & de Araujo, D. B. (2015) · PLOS ONE · doi:10.1371/journal.pone.0118143 · Cited by 454
Disruption of frontal-parietal communication by ketamine, propofol, and sevoflurane
Lee, U., Ku, S., Noh, G., Baek, S., Choi, B., & Mashour, G. A. (2013) · Anesthesiology · doi:10.1097/aln.0b013e31829103f5 · Cited by 426
Coma and consciousness: paradigms (re)framed by neuroimaging
Laureys, S., & Schiff, N. D. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.041 · Cited by 397
Self-citationIntrinsic functional connectivity differentiates minimally conscious from unresponsive patients
Athena Demertzi, A., Antonopoulos, G., Heine, L., Voss, H. U., Crone, J. S., Angeles, C. D. L., Bahri, M. A., Perri, C. D., Vanhaudenhuyse, A., Charland‐Verville, V., et al. (2015) · Brain · doi:10.1093/brain/awv169 · Cited by 398
Self-citationResting-State Functional MR Imaging: A New Window to the Brain
Barkhof, F., Haller, S., & Rombouts, S. A. R. B. (2014) · Radiology · doi:10.1148/radiol.14132388 · Cited by 397
De Havas, J. A., Parimal, S., Soon, C. S., & Chee, M. W. L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.026 · Cited by 363
EEG correlates of time-varying BOLD functional connectivity
Chang, C., Liu, Z., Chen, M. C., Liu, X., & Duyn, J. H. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.01.049 · Cited by 355
Connectivity Changes Underlying Spectral EEG Changes during Propofol-Induced Loss of Consciousness
Boly, M., Moran, R., Murphy, M., Boveroux, P., Bruno, M., Noirhomme, Q., Ledoux, D., Bonhomme, V. L., Brichant, J.-F., Tononi, G., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3769-11.2012 · Cited by 326
Self-citationConsciousness in humans and non-human animals: recent advances and future directions
Boly, M., Seth, A. K., Wilke, M., Ingmundson, P., Baars, B., Laureys, S., Edelman, D. B., & Tsuchiya, N. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00625 · Cited by 291
Self-citationEmergence delirium in children
Dahmani, S., Delivet, H., & Hilly, J. (2014) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0000000000000076 · Cited by 283
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Heine, L., Soddu, A., Gómez, F., Vanhaudenhuyse, A., Tshibanda, L., Thonnard, M., Charland-Verville, V., Kirsch, M., Laureys, S., & Demertzi, A. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00295 · Cited by 272
Self-citationConsciousness-specific dynamic interactions of brain integration and functional diversity
Luppi, A. I., Craig, M. M., Pappas, I., Finoia, P., Williams, G. B., Allanson, J., Pickard, J. D., Owen, A. M., Naci, L., Menon, D. K., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12658-9 · Cited by 251
Neurological diseases and pain
Borsook, D. (2011) · Brain · doi:10.1093/brain/awr271 · Cited by 300
General Anesthesia and Human Brain Connectivity
Hudetz, A. G. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0107 · Cited by 284
Perri, C. D., Bahri, M. A., Amico, E., Thibaut, A., Heine, L., Antonopoulos, G., Charland‐Verville, V., Wannez, S., Gómez, F. A., Hustinx, R., et al. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)00111-3 · Cited by 277
Self-citationFunctional Connectivity Measures After Psilocybin Inform a Novel Hypothesis of Early Psychosis
Carhart-Harris, R. L., Leech, R., Erritzoe, D., Williams, T. M., Stone, J. M., Evans, J., Sharp, D. J., Feilding, A., Wise, R. G., & Nutt, D. J. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs117 · Cited by 256
Neural Network Functional Connectivity During and After an Episode of Delirium
Choi, S., Lee, H., Chung, T.-S., Park, K., Jung, Y., Kim, S. I., & Kim, J. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.11060976 · Cited by 242
Emergence agitation: current knowledge and unresolved questions
Lee, S., & Sung, T. (2020) · Korean Journal of Anesthesiology · doi:10.4097/kja.20097 · Cited by 239
Temporal circuit of macroscale dynamic brain activity supports human consciousness
Huang, Z., Zhang, J., Wu, J., Mashour, G. A., & Hudetz, A. G. (2020) · Science Advances · doi:10.1126/sciadv.aaz0087 · Cited by 217
Brain functional integration decreases during propofol-induced loss of consciousness
Schrouff, J., Perlbarg, V., Boly, M., Marrelec, G., Boveroux, P., Vanhaudenhuyse, A., Bruno, M., Laureys, S., Phillips, C. L. M., Pélégrini‐Issac, M., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.04.020 · Cited by 237
Self-citationLarge-scale functional connectivity networks in the rodent brain
Gozzi, A., & Schwarz, A. J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.12.017 · Cited by 224
Cross-hemispheric functional connectivity in the human fetal brain
Thomason, M. E., Dassanayake, M. T., Shen, S., Katkuri, Y., Alexis, M., Anderson, A. L., Yeo, L., Mody, S., Hernandez-Andrade, E., Hassan, S. S., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3004978 · Cited by 225
Auditory Resting-State Network Connectivity in Tinnitus: A Functional MRI Study
Maudoux, A., Lefebvre, P. P., Cabay, J.-E., Athena Demertzi, A., Vanhaudenhuyse, A., Laureys, S., & Soddu, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036222 · Cited by 224
Self-citationJonckers, E., Audekerke, J. V., Visscher, G. D., der Linden, A. V., & Verhoye, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018876 · Cited by 228
Gao, Y., Ma, Y., Zhang, Q., Winder, A. T., Liang, Z., Antinori, L., Drew, P. J., & Zhang, N. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.069 · Cited by 226
Bonhomme, V., Vanhaudenhuyse, A., Demertzi, A., Bruno, M.-A., Jaquet, O., Bahri, M. A., Plenevaux, A., Boly, M., Boveroux, P., Soddu, A., et al. (2016) · Anesthesiology · doi:10.1097/aln.0000000000001275 · Cited by 207
Self-citationKu, S. W., Lee, U., Noh, G. J., Jun, I., & Mashour, G. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025155 · Cited by 212
Athena Demertzi, A., Gómez, F., Crone, J. S., Vanhaudenhuyse, A., Tshibanda, L., Noirhomme, Q., Thonnard, M., Charland‐Verville, V., Kirsch, M., Laureys, S., et al. (2013) · Cortex · doi:10.1016/j.cortex.2013.11.005 · Cited by 217
Self-citationReturning from oblivion: imaging the neural core of consciousness
Långsjö, J. W., Alkire, M. T., Kaskinoro, K., Hayama, H., Maksimow, A., Kaisti, K. K., Aalto, S., Aantaa, R., Jääskeläinen, S. K., Revonsuo, A., et al. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4962-11.2012 · Cited by 205
Neural correlates of unconsciousness in large-scale brain networks
Mashour, G. A., & Hudetz, A. G. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.01.003 · Cited by 189
Distributed BOLD and CBV-weighted resting-state networks in the mouse brain
Sforazzini, F., Schwarz, A. J., Galbusera, A., Bifone, A., & Gozzi, A. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.050 · Cited by 207
Spontaneous eyelid closures link vigilance fluctuation with fMRI dynamic connectivity states
Wang, C., Ong, J. L., Patanaik, A., Zhou, J. H., & Chee, M. W. L. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1523980113 · Cited by 191
Large-scale signatures of unconsciousness are consistent with a departure from critical dynamics
Tagliazucchi, E., Chialvo, D. R., Siniatchkin, M., Amico, E., Brichant, J.-F., Bonhomme, V. L., Noirhomme, Q., Laufs, H., & Laureys, S. (2016) · Journal of The Royal Society Interface · doi:10.1098/rsif.2015.1027 · Cited by 191
Self-citationIntrinsic organization of the anesthetized brain
Liang, Z., King, J., & Zhang, N. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.1020-12.2012 · Cited by 168
Akeju, O., Loggia, M. L., Catana, C., Pavone, K. J., Vazquez, R., Rhee, J., Contreras Ramirez, V., Chonde, D. B., Izquierdo-Garcia, D., Arabasz, G., et al. (2014) · eLife · doi:10.7554/elife.04499 · Cited by 168
Connectivity graph analysis of the auditory resting state network in tinnitus
Maudoux, A., Lefebvre, P. P., Cabay, J.-E., Athena Demertzi, A., Vanhaudenhuyse, A., Laureys, S., & Soddu, A. (2012) · Brain Research · doi:10.1016/j.brainres.2012.05.006 · Cited by 183
Self-citationJordan, D., Ilg, R., Riedl, V., Schorer, A., Grimberg, S., Neufang, S., Omerovic, A., Berger, S., Untergehrer, G., Preibisch, C., et al. (2013) · Anesthesiology · doi:10.1097/aln.0b013e3182a7ca92 · Cited by 180
Chai, X. J., Ofen, N., Gabrieli, J. D. E., & Whitfield, S. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00517 · Cited by 186
LSD alters dynamic integration and segregation in the human brain
Luppi, A. I., Carhart-Harris, R. L., Roseman, L., Pappas, I., Menon, D. K., & Stamatakis, E. A. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117653 · Cited by 165
Resting-state activity in development and maintenance of normal brain function
Pizoli, C. E., Shah, M. N., Snyder, A. Z., Shimony, J. S., Limbrick, D. D., Raichle, M. E., Schlaggar, B. L., & Smyth, M. D. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109144108 · Cited by 171
The Neurology of Consciousness
Tononi, G., Boly, M., Gosseries, O., & Laureys, S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800948-2.00025-x · Cited by 178
Self-citationEntropy and the Brain: An Overview
Keshmiri, S. (2020) · Entropy · doi:10.3390/e22090917 · Cited by 176
Kim, M., Mashour, G. A., Moraes, S.-B., Vanini, G., Tarnal, V., Janke, E., Hudetz, A. G., & Lee, U. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00001 · Cited by 164
Unique spatiotemporal fMRI dynamics in the awake mouse brain
Gutierrez‐Barragan, D., Singh, N. A., Alvino, F. G., Coletta, L., Rocchi, F., de Guzman, A. E., Galbusera, A., Uboldi, M., Panzeri, S., & Gozzi, A. (2022) · Current Biology · doi:10.1016/j.cub.2021.12.015 · Cited by 157
Ranft, A., Golkowski, D., Kiel, T., Riedl, V., Kohl, P., Rohrer, G., Pientka, J., Berger, S., Thul, A., Maurer, M., et al. (2016) · Anesthesiology · doi:10.1097/aln.0000000000001322 · Cited by 142
The Biology of General Anesthesia from Paramecium to Primate
Kelz, M. B., & Mashour, G. A. (2019) · Current Biology · doi:10.1016/j.cub.2019.09.071 · Cited by 151
Measuring Consciousness in Severely Damaged Brains
Gosseries, O., Di, H., Laureys, S., & Boly, M. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170339 · Cited by 153
Self-citationBarrett, A. B., Murphy, M., Bruno, M., Noirhomme, Q., Boly, M., Laureys, S., & Seth, A. K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029072 · Cited by 152
Self-citationReconfiguration of Network Hub Structure after Propofol-induced Unconsciousness
Lee, H., Mashour, G. A., Noh, G., Kim, S., & Lee, U. (2013) · Anesthesiology · doi:10.1097/aln.0b013e3182a8ec8c · Cited by 150
Liu, X., Lauer, K. K., Ward, B. D., Li, S., & Hudetz, A. G. (2012) · Anesthesiology · doi:10.1097/aln.0b013e318277a801 · Cited by 149
Threlkeld, Z. D., Bodien, Y. G., Rosenthal, E. S., Giacino, J. T., Nieto-Castañón, A., Wu, O., Whitfield, S., & Edlow, B. L. (2018) · Cortex · doi:10.1016/j.cortex.2018.05.004 · Cited by 153
Niesters, M., Khalili-Mahani, N., Martini, C., Aarts, L., van Gerven, J., van Buchem, M. A., Dahan, A., & Rombouts, S. (2012) · Anesthesiology · doi:10.1097/aln.0b013e31826a0db3 · Cited by 147
Resting-state Dynamics as a Cortical Signature of Anesthesia in Monkeys
Uhrig, L., Sitt, J. D., Jacob, A., Tasserie, J., Barttfeld, P., Dupont, M., Dehaene, S., & Jarraya, B. (2018) · Anesthesiology · doi:10.1097/aln.0000000000002336 · Cited by 131
Uehara, T., Yamasaki, T., Okamoto, T., Koike, T., Kan, S., Miyauchi, S., Kira, J.-I., & Tobimatsu, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht004 · Cited by 136
Age-dependent electroencephalogram (EEG) patterns during sevoflurane general anesthesia in infants
Cornelissen, L., Kim, S., Purdon, P. L., Brown, E. N., & Berde, C. B. (2015) · eLife · doi:10.7554/elife.06513 · Cited by 144
Schröter, M. S., Spoormaker, V. I., Schorer, A., Wohlschläger, A. M., Czisch, M., Kochs, E. F., Zimmer, C., Hemmer, B., Schneider, G. H., Jordan, D., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6046-11.2012 · Cited by 148
Kay, D. B., & Buysse, D. J. (2017) · Brain Sciences · doi:10.3390/brainsci7030023 · Cited by 149
Large-Scale Brain Networks in the Awake, Truly Resting Marmoset Monkey
Belcher, A. M., Yen, C. C., Stepp, H., Gu, H., Lu, H., Yang, Y., Silva, A. C., & Stein, E. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3146-13.2013 · Cited by 142
Dynamic Repertoire of Intrinsic Brain States Is Reduced in Propofol-Induced Unconsciousness
Hudetz, A. G., Liu, X., & Pillay, S. (2014) · Brain Connectivity · doi:10.1089/brain.2014.0230 · Cited by 145
Soddu, A., Vanhaudenhuyse, A., Bahri, M. A., Bruno, M., Boly, M., Athena Demertzi, A., Tshibanda, J., Phillips, C. L. M., Stanziano, M., Ovadia‐Caro, S., et al. (2011) · Human Brain Mapping · doi:10.1002/hbm.21249 · Cited by 145
Self-citationHutchison, R. M., Hutchison, M., Manning, K. Y., Menon, R. S., & Everling, S. (2014) · Human Brain Mapping · doi:10.1002/hbm.22583 · Cited by 141
Baker, R. H., Gent, T. C., Yang, Q., Parker, S., Vyssotski, A. L., Wisden, W., Brickley, S. G., & Franks, N. P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1519-14.2014 · Cited by 149
How are different neural networks related to consciousness?
Qin, P., Wu, X., Huang, Z., Duncan, N. W., Tang, W., Wolff, A., Hu, J., Gao, L., Jin, Y., Wu, X., et al. (2015) · Annals of Neurology · doi:10.1002/ana.24479 · Cited by 146
Monti, M. M., Lutkenhoff, E. S., Rubinov, M., Boveroux, P., Vanhaudenhuyse, A., Gosseries, O., Bruno, M., Noirhomme, Q., Boly, M., & Laureys, S. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003271 · Cited by 140
Self-citationWatching the fetal brain at ‘rest’
Schöpf, V., Kasprian, G., Brugger, P. C., & Prayer, D. (2012) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2011.10.006 · Cited by 137
Hypnotic modulation of resting state fMRI default mode and extrinsic network connectivity
Athena Demertzi, A., Soddu, A., Faymonville, M.-É., Bahri, M. A., Gosseries, O., Vanhaudenhuyse, A., Phillips, C. L. M., Maquet, P., Noirhomme, Q., Luxen, A., et al. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00020-x · Cited by 146
Self-citationTop-down mechanisms of anesthetic-induced unconsciousness
Mashour, G. A. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00115 · Cited by 138
Harmonic brain modes: a unifying framework for linking space and time in brain dynamics
Atasoy, S., Deco, G., Kringelbach, M. L., & Pearson, J. (2018) · The Neuroscientist · doi:10.1177/1073858417728032 · Cited by 124
Mashour, G. A., & Hudetz, A. G. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00044 · Cited by 133
Premotor functional connectivity predicts impulsivity in juvenile offenders
Shannon, B. J., Raichle, M. E., Snyder, A. Z., Fair, D. A., Mills, K. L., Zhang, D., Bache, K., Calhoun, V. D., Nigg, J. T., Nagel, B. J., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108241108 · Cited by 137
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Amico, E., Marinazzo, D., Perri, C. D., Heine, L., Annen, J., Martial, C., Džemidžić, M., Kirsch, M., Bonhomme, V. L., Laureys, S., et al. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.020 · Cited by 123
Self-citationBrain functional connectivity differentiates dexmedetomidine from propofol and natural sleep
Guldenmund, P., Vanhaudenhuyse, A., Sanders, R. D., SLEIGH, J. W., Bruno, M.-A., Athena Demertzi, A., Bahri, M. A., Jaquet, O., Sanfilippo, J., Baquero, K., et al. (2017) · British Journal of Anaesthesia · doi:10.1093/bja/aex257 · Cited by 133
Self-citationBlain‐Moraes, S., Lee, U., Ku, S., Noh, G., & Mashour, G. A. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00114 · Cited by 130
To wake or not to wake? The two-sided nature of the human K-complex
Jahnke, K., von Wegner, F., Morzelewski, A., Borisov, S. V., Maischein, M., Steinmetz, H., & Laufs, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.013 · Cited by 126
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Thul, A., Lechinger, J., Donis, J. A., Michitsch, G., Pichler, G., Kochs, E. F., Jordan, D., Ilg, R., & Schabus, M. (2015) · Clinical Neurophysiology · doi:10.1016/j.clinph.2015.07.039 · Cited by 127
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Liu, X., Lauer, K. K., Ward, B. D., Rao, S. M., Li, S., & Hudetz, A. G. (2011) · Human Brain Mapping · doi:10.1002/hbm.21385 · Cited by 119
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Self-citationHuang, Z., Liu, X., Mashour, G. A., & Hudetz, A. G. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2545-17.2018 · Cited by 110
Tagliazucchi, E., von Wegner, F., Morzelewski, A., Brodbeck, V., Borisov, S. V., Jahnke, K., & Laufs, H. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.073 · Cited by 114
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Self-citationResting-State Functional Magnetic Resonance Imaging
Lang, S., Duncan, N. W., & Northoff, G. (2014) · Neurosurgery · doi:10.1227/neu.0000000000000307 · Cited by 103
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Metadata
- Authors
- Boveroux, P., Vanhaudenhuyse, A., Bruno, M.-A., Noirhomme, Q., Lauwick, S., Luxen, A., Degueldre, C., Plenevaux, A., Schnakers, C., Phillips, C., Brichant, J.-F., Bonhomme, V., Maquet, P., Greicius, M. D., Laureys, S., & Boly, M.
- Affiliations
- University of Liège (BE)
- Ph.D. Student, A.R.C. Research Fellow.
- Ph.D. Student, F.N.R.S. Research Fellow.
- F.N.R.S. Postdoctoral Researcher.
- Staff Anesthesiologist.
- Professor.
- Research Assistant.
- F.N.R.S. Postdoctoral Research Fellow.
- Stanford Medicine (US)
- Professor, F.N.R.S. Senior Research Associate.
- ORCID
- Venue
- Anesthesiology
- Published
- 2010-11-01
- Volume
- 113
- Issue
- 5
- Pages
- 1038-1053
- ISSN
- 0003-3022 (ISSN-L)
- OpenAlex
- W2112639978
- Cited by
- 630
- References
- 93
- Citations by year
- 2026: 32 · 2025: 27 · 2024: 33 · 2023: 27 · 2022: 33 · 2021: 37 · 2020: 50 · 2019: 41 · 2018: 39 · 2017: 56 · 2016: 45 · 2015: 51 · 2014: 35 · 2013: 55 · 2012: 37
- FWCI
- 24.05
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Anesthesiology (publishedVersion)
- PubMed (publishedVersion)
- ORBi (University of Liège) (submittedVersion, other-oa)
- Open Repository and Bibliography (University of Liège) (submittedVersion, other-oa)
- Funders
- James S. McDonnell Foundation
- Mind Science Foundation
- European Commission
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Anesthesia and Sedative Agents
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- propofol, loss of consciousness, anesthesia, resting-state functional connectivity, thalamocortical connections, corticocortical connectivity, default mode network, frontoparietal network, frontoparietal cortex, cross-modal interaction, consciousness, consciousness recovery, sedation
- MeSH terms
- Adolescent, Adult, Consciousness, Female, Humans, Magnetic Resonance Imaging, Male, Nerve Net, Rest, Unconsciousness, Propofol, Procedural Sedation, Conscious Sedation, Deep Sedation, Young Adult
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