PMID- 37274214 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230606 IS - 1662-4548 (Print) IS - 1662-453X (Electronic) IS - 1662-453X (Linking) VI - 17 DP - 2023 TI - Cortical depth-dependent human fMRI of resting-state networks using EPIK. PG - 1151544 LID - 10.3389/fnins.2023.1151544 [doi] LID - 1151544 AB - INTRODUCTION: Recent laminar-fMRI studies have substantially improved understanding of the evoked cortical responses in multiple sub-systems; in contrast, the laminar component of resting-state networks spread over the whole brain has been less studied due to technical limitations. Animal research strongly suggests that the supragranular layers of the cortex play a critical role in maintaining communication within the default mode network (DMN); however, whether this is true in this and other human cortical networks remains unclear. METHODS: Here, we used EPIK, which offers unprecedented coverage at sub-millimeter resolution, to investigate cortical broad resting-state dynamics with depth specificity in healthy volunteers. RESULTS: Our results suggest that human DMN connectivity is primarily supported by intermediate and superficial layers of the cortex, and furthermore, the preferred cortical depth used for communication can vary from one network to another. In addition, the laminar connectivity profile of some networks showed a tendency to change upon engagement in a motor task. In line with these connectivity changes, we observed that the amplitude of the low-frequency-fluctuations (ALFF), as well as the regional homogeneity (ReHo), exhibited a different laminar slope when subjects were either performing a task or were in a resting state (less variation among laminae, i.e., lower slope, during task performance compared to rest). DISCUSSION: The identification of varied laminar profiles concerning network connectivity, ALFF, and ReHo, observed across two brain states (task vs. rest) has major implications for the characterization of network-related diseases and suggests the potential diagnostic value of laminar fMRI in psychiatric disorders, e.g., to differentiate the cortical dynamics associated with disease stages linked, or not linked, to behavioral changes. The evaluation of laminar-fMRI across the brain encompasses computational challenges; nonetheless, it enables the investigation of a new dimension of the human neocortex, which may be key to understanding neurological disorders from a novel perspective. CI - Copyright (c) 2023 Pais-Roldan, Yun, Palomero-Gallagher and Shah. FAU - Pais-Roldan, Patricia AU - Pais-Roldan P AD - Institute of Neuroscience and Medicine 4, Medical Imaging Physics, Forschungszentrum Julich, Julich, Germany. FAU - Yun, Seong Dae AU - Yun SD AD - Institute of Neuroscience and Medicine 4, Medical Imaging Physics, Forschungszentrum Julich, Julich, Germany. FAU - Palomero-Gallagher, Nicola AU - Palomero-Gallagher N AD - Institute of Neuroscience and Medicine 1, Structural and Functional Organisation of the Brain, Forschungszentrum Julich, Julich, Germany. AD - C. and O. Vogt Institute for Brain Research, Heinrich-Heine-University, Dusseldorf, Germany. AD - Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, RWTH Aachen, Aachen, Germany. FAU - Shah, N Jon AU - Shah NJ AD - Institute of Neuroscience and Medicine 4, Medical Imaging Physics, Forschungszentrum Julich, Julich, Germany. AD - Institute of Neuroscience and Medicine 11, Molecular Neuroscience and Neuroimaging, JARA, Forschungszentrum Julich, Julich, Germany. AD - JARA-BRAIN-Translational Medicine, Aachen, Germany. AD - Department of Neurology, RWTH Aachen University, Aachen, Germany. LA - eng PT - Journal Article DEP - 20230518 PL - Switzerland TA - Front Neurosci JT - Frontiers in neuroscience JID - 101478481 PMC - PMC10232833 OTO - NOTNLM OT - EPIK OT - cerebral cortex OT - cortical layer OT - high-resolution OT - resting-state fMRI COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/06/05 13:05 MHDA- 2023/06/05 13:06 PMCR- 2023/01/01 CRDT- 2023/06/05 11:59 PHST- 2023/01/26 00:00 [received] PHST- 2023/04/26 00:00 [accepted] PHST- 2023/06/05 13:06 [medline] PHST- 2023/06/05 13:05 [pubmed] PHST- 2023/06/05 11:59 [entrez] PHST- 2023/01/01 00:00 [pmc-release] AID - 10.3389/fnins.2023.1151544 [doi] PST - epublish SO - Front Neurosci. 2023 May 18;17:1151544. doi: 10.3389/fnins.2023.1151544. eCollection 2023.