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Shared functional connectome fingerprints following ritualistic ayahuasca intake.

Pablo Mallaroni, Natasha L Mason, Lilian Kloft, Johannes T Reckweg, Kim van Oorsouw, Stefan W Toennes, Hanna M Tolle, Enrico Amico, Johannes G Ramaekers

NeuroImage January 1, 2024 DOI: 10.1016/j.neuroimage.2023.120480 via PubMed

Summary

AI-generated from the abstract

Brain functional connectomes are unique fingerprints that persist across mental states, but their stability under altered states is unknown. After collective ayahuasca intake in 21 Santo Daime members, 7T fMRI showed reduced idiosyncrasy in static and dynamic functional connectivity, with a spatiotemporal reallocation of keypoint edges. Interindividual differences in higher-order connectivity motifs predicted perceptual drug effects, demonstrating that individualized connectivity markers can trace a subject's functional connectome across altered states of consciousness.

Study at a glance

Characteristics Within-subject study Peer reviewed
Sample size 21
Population Santo Daime members
Intervention Ayahuasca
Duration Acute
Topics Ayahuasca DMT
Keywords Entheogens Brain connectivity connectome Neuroimaging FMRI Brain scanning Connectome fingerprints
Citations 17
Key finding Ayahuasca reduces the idiosyncrasy of functional connectomes and reallocates keypoint edges, with interindividual differences in higher-order connectivity motifs predicting perceptual drug effects.

Abstract

The knowledge that brain functional connectomes are unique and reliable has enabled behaviourally relevant inferences at a subject level. However, whether such "fingerprints" persist under altered states of consciousness is unknown. Ayahuasca is a potent serotonergic psychedelic which produces a widespread dysregulation of functional connectivity. Used communally in religious ceremonies, its shared use may highlight relevant novel interactions between mental state and functional connectome (FC) idiosyncrasy. Using 7T fMRI, we assessed resting-state static and dynamic FCs for 21 Santo Daime members after collective ayahuasca intake in an acute, within-subject study. Here, connectome fingerprinting revealed FCs showed reduced idiosyncrasy, accompanied by a spatiotemporal reallocation of keypoint edges. Importantly, we show that interindividual differences in higher-order FC motifs are relevant to experiential phenotypes, given that they can predict perceptual drug effects. Collectively, our findings offer an example of how individualised connectivity markers can be used to trace a subject's FC across altered states of consciousness.

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