Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects. / Olsen, Anders S; Lykkebo-Valløe, Anders; Ozenne, Brice; Madsen, Martin K; Stenbæk, Dea S; Armand, Sophia; Mørup, Morten; Ganz, Melanie; Knudsen, Gitte M; Fisher, Patrick M.

In: NeuroImage, Vol. 264, 119716, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Olsen, AS, Lykkebo-Valløe, A, Ozenne, B, Madsen, MK, Stenbæk, DS, Armand, S, Mørup, M, Ganz, M, Knudsen, GM & Fisher, PM 2022, 'Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects', NeuroImage, vol. 264, 119716. https://doi.org/10.1016/j.neuroimage.2022.119716

APA

Olsen, A. S., Lykkebo-Valløe, A., Ozenne, B., Madsen, M. K., Stenbæk, D. S., Armand, S., Mørup, M., Ganz, M., Knudsen, G. M., & Fisher, P. M. (2022). Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects. NeuroImage, 264, [119716]. https://doi.org/10.1016/j.neuroimage.2022.119716

Vancouver

Olsen AS, Lykkebo-Valløe A, Ozenne B, Madsen MK, Stenbæk DS, Armand S et al. Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects. NeuroImage. 2022;264. 119716. https://doi.org/10.1016/j.neuroimage.2022.119716

Author

Olsen, Anders S ; Lykkebo-Valløe, Anders ; Ozenne, Brice ; Madsen, Martin K ; Stenbæk, Dea S ; Armand, Sophia ; Mørup, Morten ; Ganz, Melanie ; Knudsen, Gitte M ; Fisher, Patrick M. / Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects. In: NeuroImage. 2022 ; Vol. 264.

Bibtex

@article{4f23f7f38a724df2ac81ac194197a16b,
title = "Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects",
abstract = "BACKGROUND: Psilocin, the neuroactive metabolite of psilocybin, is a serotonergic psychedelic that induces an acute altered state of consciousness, evokes lasting changes in mood and personality in healthy individuals, and has potential as an antidepressant treatment. Examining the acute effects of psilocin on resting-state time-varying functional connectivity implicates network-level connectivity motifs that may underlie acute and lasting behavioral and clinical effects.AIM: Evaluate the association between resting-state time-varying functional connectivity (tvFC) characteristics and plasma psilocin level (PPL) and subjective drug intensity (SDI) before and right after intake of a psychedelic dose of psilocybin in healthy humans.METHODS: Fifteen healthy individuals completed the study. Before and at multiple time points after psilocybin intake, we acquired 10-minute resting-state blood-oxygen-level-dependent functional magnetic resonance imaging scans. Leading Eigenvector Dynamics Analysis (LEiDA) and diametrical clustering were applied to estimate discrete, sequentially active brain states. We evaluated associations between the fractional occurrence of brain states during a scan session and PPL and SDI using linear mixed-effects models. We examined associations between brain state dwell time and PPL and SDI using frailty Cox proportional hazards survival analysis.RESULTS: Fractional occurrences for two brain states characterized by lateral frontoparietal and medial fronto-parietal-cingulate coherence were statistically significantly negatively associated with PPL and SDI. Dwell time for these brain states was negatively associated with SDI and, to a lesser extent, PPL. Conversely, fractional occurrence and dwell time of a fully connected brain state partly associated with motion was positively associated with PPL and SDI.CONCLUSION: Our findings suggest that the acute perceptual psychedelic effects induced by psilocybin may stem from drug-level associated decreases in the occurrence and duration of lateral and medial frontoparietal connectivity motifs. We apply and argue for a modified approach to modeling eigenvectors produced by LEiDA that more fully acknowledges their underlying structure. Together these findings contribute to a more comprehensive neurobiological framework underlying acute effects of serotonergic psychedelics.",
author = "Olsen, {Anders S} and Anders Lykkebo-Vall{\o}e and Brice Ozenne and Madsen, {Martin K} and Stenb{\ae}k, {Dea S} and Sophia Armand and Morten M{\o}rup and Melanie Ganz and Knudsen, {Gitte M} and Fisher, {Patrick M}",
note = "Copyright {\textcopyright} 2022. Published by Elsevier Inc.",
year = "2022",
doi = "10.1016/j.neuroimage.2022.119716",
language = "English",
volume = "264",
journal = "NeuroImage",
issn = "1053-8119",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Psilocybin modulation of time-varying functional connectivity is associated with plasma psilocin and subjective effects

AU - Olsen, Anders S

AU - Lykkebo-Valløe, Anders

AU - Ozenne, Brice

AU - Madsen, Martin K

AU - Stenbæk, Dea S

AU - Armand, Sophia

AU - Mørup, Morten

AU - Ganz, Melanie

AU - Knudsen, Gitte M

AU - Fisher, Patrick M

N1 - Copyright © 2022. Published by Elsevier Inc.

PY - 2022

Y1 - 2022

N2 - BACKGROUND: Psilocin, the neuroactive metabolite of psilocybin, is a serotonergic psychedelic that induces an acute altered state of consciousness, evokes lasting changes in mood and personality in healthy individuals, and has potential as an antidepressant treatment. Examining the acute effects of psilocin on resting-state time-varying functional connectivity implicates network-level connectivity motifs that may underlie acute and lasting behavioral and clinical effects.AIM: Evaluate the association between resting-state time-varying functional connectivity (tvFC) characteristics and plasma psilocin level (PPL) and subjective drug intensity (SDI) before and right after intake of a psychedelic dose of psilocybin in healthy humans.METHODS: Fifteen healthy individuals completed the study. Before and at multiple time points after psilocybin intake, we acquired 10-minute resting-state blood-oxygen-level-dependent functional magnetic resonance imaging scans. Leading Eigenvector Dynamics Analysis (LEiDA) and diametrical clustering were applied to estimate discrete, sequentially active brain states. We evaluated associations between the fractional occurrence of brain states during a scan session and PPL and SDI using linear mixed-effects models. We examined associations between brain state dwell time and PPL and SDI using frailty Cox proportional hazards survival analysis.RESULTS: Fractional occurrences for two brain states characterized by lateral frontoparietal and medial fronto-parietal-cingulate coherence were statistically significantly negatively associated with PPL and SDI. Dwell time for these brain states was negatively associated with SDI and, to a lesser extent, PPL. Conversely, fractional occurrence and dwell time of a fully connected brain state partly associated with motion was positively associated with PPL and SDI.CONCLUSION: Our findings suggest that the acute perceptual psychedelic effects induced by psilocybin may stem from drug-level associated decreases in the occurrence and duration of lateral and medial frontoparietal connectivity motifs. We apply and argue for a modified approach to modeling eigenvectors produced by LEiDA that more fully acknowledges their underlying structure. Together these findings contribute to a more comprehensive neurobiological framework underlying acute effects of serotonergic psychedelics.

AB - BACKGROUND: Psilocin, the neuroactive metabolite of psilocybin, is a serotonergic psychedelic that induces an acute altered state of consciousness, evokes lasting changes in mood and personality in healthy individuals, and has potential as an antidepressant treatment. Examining the acute effects of psilocin on resting-state time-varying functional connectivity implicates network-level connectivity motifs that may underlie acute and lasting behavioral and clinical effects.AIM: Evaluate the association between resting-state time-varying functional connectivity (tvFC) characteristics and plasma psilocin level (PPL) and subjective drug intensity (SDI) before and right after intake of a psychedelic dose of psilocybin in healthy humans.METHODS: Fifteen healthy individuals completed the study. Before and at multiple time points after psilocybin intake, we acquired 10-minute resting-state blood-oxygen-level-dependent functional magnetic resonance imaging scans. Leading Eigenvector Dynamics Analysis (LEiDA) and diametrical clustering were applied to estimate discrete, sequentially active brain states. We evaluated associations between the fractional occurrence of brain states during a scan session and PPL and SDI using linear mixed-effects models. We examined associations between brain state dwell time and PPL and SDI using frailty Cox proportional hazards survival analysis.RESULTS: Fractional occurrences for two brain states characterized by lateral frontoparietal and medial fronto-parietal-cingulate coherence were statistically significantly negatively associated with PPL and SDI. Dwell time for these brain states was negatively associated with SDI and, to a lesser extent, PPL. Conversely, fractional occurrence and dwell time of a fully connected brain state partly associated with motion was positively associated with PPL and SDI.CONCLUSION: Our findings suggest that the acute perceptual psychedelic effects induced by psilocybin may stem from drug-level associated decreases in the occurrence and duration of lateral and medial frontoparietal connectivity motifs. We apply and argue for a modified approach to modeling eigenvectors produced by LEiDA that more fully acknowledges their underlying structure. Together these findings contribute to a more comprehensive neurobiological framework underlying acute effects of serotonergic psychedelics.

U2 - 10.1016/j.neuroimage.2022.119716

DO - 10.1016/j.neuroimage.2022.119716

M3 - Journal article

C2 - 36341951

VL - 264

JO - NeuroImage

JF - NeuroImage

SN - 1053-8119

M1 - 119716

ER -

ID: 325333752