Linking human brain functional connectivity to underlying neurotransmitter systems
Leon D. LotteriD, Golia ShafieiiD, Daouia I. LarabiiD, Abhay KoushikiD, Ottavia DipasqualeiD, Mitul Ashok MehtaiD, Mara CercignaniiD, Arjun SethiiD, Neil Andrew HarrisoniD, Štefan HoligaiD, Daniel UmbrichtiD, Igor Y. YakusheviD, Suresh D MuthukumaraswamyiD, Anna ForsythiD, Joerg F. HippiD, Bratislav MišićiD, Svenja CaspersiD, Julian KoenigiD, Kaustubh R. PatiliD, Casey PaquolaiD, Simon Bodo EickhoffiD, Juergen DukartiD
Abstract
The human brain is organized into interacting functional systems. Their underlying neurobiological mechanisms remain difficult to study in vivo. Here, we adopt a topological framework to quantify the association between neurobiology and brain functional connectivity derived from both resting-state fMRI and MEG. Across six healthy adult cohorts (n = 19-112), regional variation in fMRI connectivity robustly aligns with the distribution of neurotransmitter receptors and transporters. These patterns are present in every single subject, replicate across all cohorts, and are mirrored in MEG. Most prominently, noradrenergic modulation of connectivity in a sensorimotor-insular network is consistently detected across individuals and linked to autonomic arousal. In pharmacological and clinical samples, associations are sensitive to neurotransmitter system manipulation and are altered in early psychosis, aligning with clinical symptomatology. These findings provide biological insight into typical and atypical functional organization of the human brain using a framework linking underlying neurobiology to the functional connectome (NEOFC).
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