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Atalay, A. S.

Publications and source records attributed to Atalay, A. S..

3 recordsLinked to original sources

Functional fractionation of large-scale brain networks in the human subcortex

Brain network mapping plays a crucial role in advancing our understanding of human brain organization and the neuroanatomic foundations of cognition. Historically, the identification of large-scale brain networks has focused on the cerebral cortex. Some cortical networks have been fractionated into subnetworks, yielding valuable insights into their domain-specific cognitive functions. In contrast, functional mapping of large-scale brain networks within subcortical regions remains an emerging and challenging field, hindered by a low signal-to-noise ratio in subcortical functional MRI data and an inability to distinguish networks with substantial spatiotemporal overlap. In this study, we fractionated and identified fifteen spatially overlapped and temporally correlated subnetworks, which can be categorized into four large-scale brain networks. The subcortical functional connectivity patterns of these subnetworks exhibited distinct, yet overlapping, spatial configurations, with widely connected hub nodes identified in the caudate, putamen, hippocampus, and thalamus. These subnetworks are highly reproducible across healthy human brains and provide normative functional atlases, which we release here as a resource for the academic community. As a proof-of-principle demonstration of how the atlases can be used to elucidate the pathophysiology of neuropsychiatric disorders, we show that the spatial patterns of the subnetworks predict the level of consciousness in patients with severe traumatic brain injury. These observations indicate a highly conserved and spatially overlapped subcortical functional architecture in the human brain, providing opportunities to elucidate pathophysiologic mechanisms and develop new neuromodulatory therapies for a broad spectrum of neuropsychiatric diseases.

neuroscience↗

Visualizing Effective Connectivity in the Human Brain

To enhance mechanistic understanding of effective connectivity in the human brain, we created a tool that links high-temporal resolution transcranial magnetic stimulation electroencephalography (TMS-EEG) with high-spatial resolution diffusion MRI. This tool, Surface to Tractography Real-time EEG Activation Mapping in 4 Dimensions (STREAM-4D), integrates electrophysiologic source estimation models from TMS-evoked potentials (TEPs) with structural connectivity models from diffusion MRI tractography. In a proof-of-principle application, we used STREAM-4D to analyze TMS-EEG and diffusion MRI tractography data in a neurotypical subject across three stimulation sites: premotor, parietal, and occipital cortex. STREAM-4D revealed extensive structural connections associated with the TMS-evoked source models, involving thalamocortical, ipsilateral cortico-cortical, and transcallosal cortico-cortical connections. Activity-weighted structural connectivity differed for the three stimulation sites but shared two extensively connected nodes: the ipsilateral thalamus and putamen. STREAM-4D provides opportunities to elucidate how electrical activity evoked by a TMS pulse is related to underlying white matter architecture.

neuroscience↗

Developmental Ramifications of the Screen Age: Associations between Screen Time and Neural Maturation in a Massive Adolescent Cohort

A growing body of literature associates increases in electronic screen time with a vast array of psychological consequences amongst adolescents, but little is known about the neurological underpinnings of this relationship. This longitudinal study examines structural and diffusion brain MRI scans from the Adolescent Brain Cognitive Development (ABCD)Study: a large multi-site study with thousands of participants. By assessing both gray matter density (GMD) and grey matter measurements of diffusion microstructure in the adolescent brain, we describe how the developmental trajectory of the brain changes with screen-based media consumption at the sub-cellular level. Grey matter microstructure was measured across 13 bilateral regions functionally implicated with screen time use, and associated with either the control or reward system. After controlling for age, sex, total brain volume, scanning site, sibling relationships, physical activity, and socioeconomic status, this study finds significant positive correlations between increased screen time and axonal signal across 6 of the 13 regions while also finding significantly decreased intracellular signal in 8 regions. Comparing these associations to normal developmental trajectories suggests adolescent age-related brain development may be accelerated by increased screen time in brain areas associated with reward processing while age-related brain development may be decelerated in regions of the control system. Highlighting the sensitivity of microstructural analysis, no significant cross-sectional or longitudinal relationship with increased screen time was found using GMD, or fractional anisotropy. This work suggests that increased screen usage during adolescent development has a complex association with brain tissue that cannot be completely described by traditional quantifications of tissue microstructure.

neuroscience↗