Evidence map›Paper›PMID 42282806›Full record

ArticlebioRxiv : the preprint server for biology2026

Reorganization of Human Brain Waves Across Diverse States of Consciousness.

Panagiotis Fotiadis, Hyunwoo Jang, Rui Dai, Duan Li, Rodrigo Cofré, Christopher Timmermann, George A Mashour, Anthony G Hudetz, Zirui Huang

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Panagiotis FotiadisDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0001-7287-9227
Hyunwoo JangCenter for Consciousness Science, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0003-3881-0159
Rui DaiDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, USA.
Duan LiDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, USA.
Rodrigo CofréCRONOS Team, Inria Centre, Université Côte d'Azur, Sophia Antipolis, France.
Christopher TimmermannCentre for Consciousness Research, Department of Experimental Psychology, University College London, London, United Kingdom.
George A MashourDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, USA.
Anthony G HudetzDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, USA.
Zirui HuangDepartment of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0002-5949-0206

Funding

Neuroimaging of Anesthetic Modulation of Human ConsciousnessR01GM103894 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Zirui Huang, Anthony George Hudetz · 2013 to 2026
$4.0M
Michigan Translational Imaging Program (M-TIP)T32EB035504 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Vikas Gulani, Peter James Henry Scott · 2025 to 2026
$552k
NIBIB NIH HHS T32 EB035504NIGMS NIH HHS R01 GM103894
6 · The paper itself

Abstract

Brain waves are ubiquitous phenomena of human brain activity. As they propagate, they coordinate neural communication, shaping conscious perception. Understanding how brain waves unfold across space and time is thus critical for uncovering the neural mechanisms that support and suppress consciousness. Here, we analyzed data from the Human Connectome Project alongside multiple independent human datasets of various states of consciousness collected during non-rapid eye movement sleep, propofol anesthesia, and psychedelic states produced by lysergic acid diethylamide, N,N-dimethyltryptamine, psilocybin, nitrous oxide, and ketamine. We then applied complex principal component analysis to map spatiotemporal propagation patterns of blood oxygen level-dependent activity across the human brain, under these diverse states of consciousness. We identified four dominant motifs of wave propagation: a global synchronized wave supporting unimodal-transmodal propagation, an anti-correlated unimodal-transmodal wave, an anti-correlated task-positive/task-negative wave, and an anti-correlated visual-somatomotor wave. Among them, the global wave exhibited the most pronounced state-dependent reconfiguration: in diminished states (sleep and anesthesia), the time needed for the wave to propagate across brain regions consistently increased and the distribution of regional contributions to the wave's power became more spatially concentrated and heterogeneous across individuals, indicating slower, more fragmented, and less stereotyped dynamics. In contrast, propagation duration decreased under psychedelic states, reflecting accelerated global wave dynamics alongside a trend towards more spatially distributed and uniform regional contributions, consistent with a more integrated global wave propagation pattern. Beyond this global mode, diminished states slowed propagation primarily along the unimodal-transmodal axis, whereas psychedelic states selectively accelerated propagation along the task-positive/task-negative axis. Together, our findings reveal that diminished (sleep and anesthesia) and psychedelic states alter the spatiotemporal structure of wave propagation across the brain in opposite and distinct ways, providing a unifying account of how macroscale brain dynamics are dynamically reshaped under pharmacological and endogenous perturbations of consciousness.

Identifiers

PMID42282806
PMCPMC13252131

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.