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A comprehensive map of the structural connectome in the human brain has been a coveted resource for understanding macroscopic brain networks. Here we report an expert-vetted, population-averaged atlas of the structural connectome derived from diffusion MRI data (N = 842). This was achieved by creating a high-resolution template of diffusion patterns averaged across individual subjects and using tractography to generate 550,000 trajectories of representative white matter fascicles annotated by 80 anatomical labels. The trajectories were subsequently clustered and labeled by a team of experienced neuroanatomists in order to conform to prior neuroanatomical knowledge. A multi-level network topology was then described using whole-brain connectograms, with subdivisions of the association pathways showing small-worldness in intra-hemisphere connections, projection pathways showing hub structures at thalamus, putamen, and brainstem, and commissural pathways showing bridges connecting cerebral hemispheres to provide global efficiency. This atlas of the structural connectome provides representative organization of human brain white matter, complementary to traditional histologically-derived and voxel-based white matter atlases, allowing for better modeling and simulation of brain connectivity for future connectome studies.

Advances in understanding the structural connectomes of human brain require improved approaches for the construction, comparison and integration of high-dimensional whole-brain tractography data from a large number of individuals. This article develops a population-based structural connectome (PSC) mapping framework to address these challenges. PSC simultaneously characterizes a large number of white matter bundles within and across different subjects by registering different subjects’ brains based on coarse cortical parcellations, compressing the bundles of each connection, and extracting novel connection weights. A robust tractography algorithm and streamline post-processing techniques, including dilation of gray matter regions, streamline cutting, and outlier streamline removal are applied to improve the robustness of the extracted structural connectomes. The developed PSC framework can be used to reproducibly extract binary networks, weighted networks and streamline-based brain connectomes. We apply the PSC to Human Connectome Project data to illustrate its application in characterizing normal variations and heritability of structural connectomes in healthy subjects. •Construction, comparison and integration of high-dimensional whole-brain tractographic data.•Extract binary networks, weighted networks and streamline-based connectivity representations of brain connectomes.•Relating structural connectomes to demographic and behavioral measures.•A test-retest dataset for validation.•A comprehensive Human Connectome Project (HCP) data analysis results.•The package for PSC, along with its documentation, is freely accessible from the nitric and bigs2 websites.

Diffusion MRI streamlines tractography is increasingly being used to characterise and assess the structural connectome of the human brain. However, issues pertaining to quantification of structural connectivity using streamlines reconstructions are well-established in the field, and therefore the validity of any conclusions that may be drawn from these analyses remains ambiguous. We recently proposed a post-processing method entitled “SIFT: Spherical-deconvolution Informed Filtering of Tractograms” as a mechanism for reducing the biases in quantitative measures of connectivity introduced by the streamlines reconstruction method. Here, we demonstrate the advantage of this approach in the context of connectomics in three steps. Firstly, we carefully consider the model imposed by the SIFT method, and the implications this has for connectivity quantification. Secondly, we investigate the effects of SIFT on the reproducibility of structural connectome construction. Thirdly, we compare quantitative measures extracted from structural connectomes derived from streamlines tractography, with and without the application of SIFT, to published estimates drawn from post-mortem brain dissection. The combination of these sources of evidence demonstrates the important role the SIFT methodology has for the robust quantification of structural connectivity of the brain using diffusion MRI. •Evaluated effects of SIFT method on quantitative tractography applications•Synthetic phantom demonstrates vital importance of SIFT.•SIFT reduces scan–rescan variability of structural connectome construction.•SIFT improves biological accuracy of structural connectome.

•We associated structural brain organization with time-varying functional dynamics.•Structure-function coupling is strong for transitions involving sensorimotor states.•Sensorimotor transitions involve network diffusion along structural connectome gradients.•Transitions in higher-order states increasingly engage inter-hub routing. Human cognition is dynamic, alternating over time between externally-focused states and more abstract, often self-generated, patterns of thought. Although cognitive neuroscience has documented how networks anchor particular modes of brain function, mechanisms that describe transitions between distinct functional states remain poorly understood. Here, we examined how time-varying changes in brain function emerge within the constraints imposed by macroscale structural network organization. Studying a large cohort of healthy adults (n = 326), we capitalized on manifold learning techniques that identify low dimensional representations of structural connectome organization and we decomposed neurophysiological activity into distinct functional states and their transition patterns using Hidden Markov Models. Structural connectome organization predicted dynamic transitions anchored in sensorimotor systems and those between sensorimotor and transmodal states. Connectome topology analyses revealed that transitions involving sensorimotor states traversed short and intermediary distances and adhered strongly to communication mechanisms of network diffusion. Conversely, transitions between transmodal states involved spatially distributed hubs and increasingly engaged long-range routing. These findings establish that the structure of the cortex is optimized to allow neural states the freedom to vary between distinct modes of processing, and so provides a key insight into the neural mechanisms that give rise to the flexibility of human cognition.

Diffusion MRI‐based structural connectomes are increasingly used to investigate brain connectivity changes associated with various disorders. However, small sample sizes in individual studies, along with highly heterogeneous disorder‐related manifestations, underscore the need to pool datasets across multiple studies to be able to identify coherent and generalizable connectivity patterns linked to these disorders. Yet, combining datasets introduces site‐related differences due to variations in scanner hardware or acquisition protocols. These differences highlight the necessity for statistical data harmonization to mitigate site‐related effects on structural connectomes while preserving the biological information associated with participant demographics and the disorders. While several paradigms exist for harmonizing normally distributed neuroimaging measures, this paper represents the first effort to establish a harmonization framework specifically tailored for the structural connectome. We conduct a thorough investigation of various statistical harmonization methods, adapting them to accommodate the unique distributional characteristics and graph‐based properties of structural connectomes. Through rigorous evaluation, we show that our MATCH algorithm, based on the gamma‐distributed model, consistently outperforms existing approaches in modeling structural connectomes, enabling the effective removal of site‐related biases in both edge‐based and downstream graph analyses while preserving biological variability. Two real‐world applications further highlight the utility of our harmonization framework in addressing challenges in multi‐site structural connectome analysis. Specifically, harmonization with MATCH enhances the generalizability of connectome‐based machine learning predictors to new datasets and increases statistical power for detecting group‐level differences. Our work provides essential guidelines for harmonizing multi‐site structural connectomes, paving the way for more robust discoveries through collaborative research in the era of team science and big data. As big data drives collaboration across institutions, this study tackles the challenge of merging multi‐site structural connectome data while minimizing site‐related biases. We present a pioneering harmonization framework, MATCH, tailored to structural connectomes, offering essential guidelines to facilitate multi‐site data integration to yield more robust, replicable, and generalizable findings.

Diffusion MRI fiber tracking provides a non-invasive method for mapping the trajectories of human brain connections, but its false connection problem has been a major challenge. This study introduces topology-informed pruning (TIP), a method that automatically identifies singular tracts and eliminates them to improve the tracking accuracy. The accuracy of the tractography with and without TIP was evaluated by a team of 6 neuroanatomists in a blinded setting to examine whether TIP could improve the accuracy. The results showed that TIP improved the tracking accuracy by 11.93% in the single-shell scheme and by 3.47% in the grid scheme. The improvement is significantly different from a random pruning (p value < 0.001). The diagnostic agreement between TIP and neuroanatomists was comparable to the agreement between neuroanatomists. The proposed TIP algorithm can be used to automatically clean-up noisy fibers in deterministic tractography, with a potential to confirm the existence of a fiber connection in basic neuroanatomical studies or clinical neurosurgical planning.

Ongoing brain function is largely determined by the underlying wiring of the brain, but the specific rules governing this relationship remain unknown. Emerging literature has suggested that functional interactions between brain regions emerge from the structural connections through mono- as well as polysynaptic mechanisms. Here, we propose a novel approach based on diffusion maps and Riemannian optimization to emulate this dynamic mechanism in the form of random walks on the structural connectome and predict functional interactions as a weighted combination of these random walks. Our proposed approach was evaluated in two different cohorts of healthy adults (Human Connectome Project, HCP; Microstructure-Informed Connectomics, MICs). Our approach outperformed existing approaches and showed that performance plateaus approximately around the third random walk. At macroscale, we found that the largest number of walks was required in nodes of the default mode and frontoparietal networks, underscoring an increasing relevance of polysynaptic communication mechanisms in transmodal cortical networks compared to primary and unimodal systems.

•A computational framework that jointly embeds both functional and structural connectomes.•A method to predict structural connectome from structural one.•Multimodal brain connectivity analysis and differences between diseased and healthy populations. Understanding the connection between the brain’s structural connectivity and its functional connectivity is of immense interest in computational neuroscience. Although some studies have suggested that whole brain functional connectivity is shaped by the underlying structure, the rule by which anatomy constraints brain dynamics remains an open question. In this work, we introduce a computational framework that identifies a joint subspace of eigenmodes for both functional and structural connectomes. We found that a small number of those eigenmodes are sufficient to reconstruct functional connectivity from the structural connectome, thus serving as low-dimensional basis function set. We then develop an algorithm that can estimate the functional eigen spectrum in this joint space from the structural eigen spectrum. By concurrently estimating the joint eigenmodes and the functional eigen spectrum, we can reconstruct a given subject’s functional connectivity from their structural connectome. We perform elaborate experiments and demonstrate that the proposed algorithm for estimating functional connectivity from the structural connectome using joint space eigenmodes gives competitive performance as compared to the existing benchmark methods with better interpretability.

Recent graph-theoretical studies of Parkinson's disease (PD) have examined alterations in the global properties of the brain structural connectome; however, reported alterations are not consistent. The present study aimed to identify the most robust global metric alterations in PD via a meta-analysis. A comprehensive literature search was conducted for all available diffusion MRI structural connectome studies that compared global graph metrics between PD patients and healthy controls (HC). Hedges’ g effect sizes were calculated for each study and then pooled using a random-effects model in Comprehensive Meta-Analysis software, and the effects of potential moderator variables were tested. A total of 22 studies met the inclusion criteria for review. Of these, 16 studies reporting 10 global graph metrics (916 PD patients; 560 HC) were included in the meta-analysis. In the structural connectome of PD patients compared with HC, we found a significant decrease in clustering coefficient (g = -0.357, P = 0.005) and global efficiency (g = -0.359, P < 0.001), and a significant increase in characteristic path length (g = 0.250, P = 0.006). Dopaminergic medication, sex and age of patients were potential moderators of global brain network changes in PD. These findings provide evidence of decreased global segregation and integration of the structural connectome in PD, indicating a shift from a balanced small-world network to ‘weaker small-worldization’, which may provide useful markers of the pathophysiological mechanisms underlying PD.

When using diffusion MRI streamlines tractograms to construct structural connectomes, ideally, each streamline should connect exactly 2 regions-of-interest (i.e. network nodes) as defined by a given brain parcellation scheme. However, the ill-posed nature of termination criteria in many tractography algorithms can cause streamlines apparently being associated with zero, one, or more than two grey matter (GM) nodes; streamlines that terminate in white matter or cerebrospinal fluid may even end up being assigned to nodes if the definitions of these nodes are not strictly constrained to genuine GM areas, resulting in a misleading connectome in non-trivial ways. Based on both in-house MRI data and state-of-the-art data provided by the Human Connectome Project, this study investigates the actual influence of streamline-to-node assignment methods, and their interactions with fibre-tracking terminations and brain parcellations, on the construction of pairwise regional connectivity and subsequent connectomic measures. Our results show that the frequency of generating successful pairwise connectivity is heavily affected by the convoluted interactions between the applied strategies for connectome construction, and that minor changes in the mechanism can cause significant variations in the within- and between-module connectivity strengths as well as in the commonly-used graph theory metrics. Our data suggest that these fundamental processes should not be overlooked in structural connectomics research, and that improved data quality is not in itself sufficient to solve the underlying problems associated with assigning streamlines to brain nodes. We demonstrate that the application of advanced fibre-tracking techniques that are designed to correct for inaccuracies of track terminations with respect to anatomical information at the fibre-tracking stage is advantageous to the subsequent connectome construction process, in which pairs of parcellation nodes can be more robustly identified from streamline terminations via a suitable assignment mechanism. •The process of assigning streamlines to brain nodes can be a significant problem.•Using over-dilated node images may result in biologically unrealistic connections.•Connectome topology is significantly affected by connection construction mechanisms.•Improved data quality cannot fix the underlying issues of connectome construction.•Advanced tractography methods can improve the construction of pairwise connections.