scholarly journals Topological organization of the human brain functional connectome across the lifespan

2014 ◽  
Vol 7 ◽  
pp. 76-93 ◽  
Author(s):  
Miao Cao ◽  
Jin-Hui Wang ◽  
Zheng-Jia Dai ◽  
Xiao-Yan Cao ◽  
Li-Li Jiang ◽  
...  
2019 ◽  
Vol Volume 15 ◽  
pp. 2487-2502 ◽  
Author(s):  
Xin Huang ◽  
Yan Tong ◽  
Chen-Xing Qi ◽  
Yang-Tao Xu ◽  
Han-Dong Dan ◽  
...  

2020 ◽  
Vol 4 (3) ◽  
pp. 925-945
Author(s):  
Leonardo Tozzi ◽  
Scott L. Fleming ◽  
Zachary D. Taylor ◽  
Cooper D. Raterink ◽  
Leanne M. Williams

Countless studies have advanced our understanding of the human brain and its organization by using functional magnetic resonance imaging (fMRI) to derive network representations of human brain function. However, we do not know to what extent these “functional connectomes” are reliable over time. In a large public sample of healthy participants ( N = 833) scanned on two consecutive days, we assessed the test-retest reliability of fMRI functional connectivity and the consequences on reliability of three common sources of variation in analysis workflows: atlas choice, global signal regression, and thresholding. By adopting the intraclass correlation coefficient as a metric, we demonstrate that only a small portion of the functional connectome is characterized by good (6–8%) to excellent (0.08–0.14%) reliability. Connectivity between prefrontal, parietal, and temporal areas is especially reliable, but also average connectivity within known networks has good reliability. In general, while unreliable edges are weak, reliable edges are not necessarily strong. Methodologically, reliability of edges varies between atlases, global signal regression decreases reliability for networks and most edges (but increases it for some), and thresholding based on connection strength reduces reliability. Focusing on the reliable portion of the connectome could help quantify brain trait-like features and investigate individual differences using functional neuroimaging.


2020 ◽  
Vol 4 (3) ◽  
pp. 698-713 ◽  
Author(s):  
Meenusree Rajapandian ◽  
Enrico Amico ◽  
Kausar Abbas ◽  
Mario Ventresca ◽  
Joaquín Goñi

The identifiability framework (𝕀 f) has been shown to improve differential identifiability (reliability across-sessions and -sites, and differentiability across-subjects) of functional connectomes for a variety of fMRI tasks. But having a robust single session/subject functional connectome is just the starting point to subsequently assess network properties for characterizing properties of integration, segregation, and communicability, among others. Naturally, one wonders whether uncovering identifiability at the connectome level also uncovers identifiability on the derived network properties. This also raises the question of where to apply the 𝕀 f framework: on the connectivity data or directly on each network measurement? Our work answers these questions by exploring the differential identifiability profiles of network measures when 𝕀 f is applied (a) on the functional connectomes, and (b) directly on derived network measurements. Results show that improving across-session reliability of functional connectomes (FCs) also improves reliability of derived network measures. We also find that, for specific network properties, application of 𝕀 f directly on network properties is more effective. Finally, we discover that applying the framework, either way, increases task sensitivity of network properties. At a time when the neuroscientific community is focused on subject-level inferences, this framework is able to uncover FC fingerprints, which propagate to derived network properties.


2019 ◽  
Author(s):  
Andreas Horn ◽  
Gregor Wenzel ◽  
Friederike Irmen ◽  
Julius Hübl ◽  
Ningfei Li ◽  
...  

AbstractNeuroimaging has seen a paradigm shift from a formal description of local activity patterns toward studying distributed brain networks. The recently defined framework of the ‘human connectome’ allows to globally analyse parts of the brain and their interconnections. Deep brain stimulation (DBS) is an invasive therapy for patients with severe movement disorders aiming to retune abnormal brain network activity by local high frequency stimulation of the basal ganglia. Beyond clinical utility, DBS represents a powerful research platform to study functional connectomics and the modulation of distributed brain networks in the human brain. We acquired resting-state functional MRI in twenty Parkinson’s disease (PD) patients with subthalamic DBS switched ON and OFF. An age-matched control cohort of fifteen subjects was acquired from an open data repository. DBS lead placement in the subthalamic nucleus (STN) was localized using a state-of-the art pipeline that involved brain shift correction, multispectral image registration and use of a precise subcortical atlas. Based on a realistic 3D model of the electrode and surrounding anatomy, the amount of local impact of DBS was estimated using a finite element method approach. On a global level, average connectivity increases and decreases throughout the brain were estimated by contrasting ON and OFF DBS scans on a voxel-wise graph comprising eight thousand nodes. Local impact of DBS on the sensorimotor STN explained half the variance in global connectivity increases within the sensorimotor network (R = 0.711, p < 0.001). Moreover, local impact of DBS on the motor STN could explain the degree of how much voxel-wise average brain connectivity normalized toward healthy controls (R = 0.713, p < 0.001). Finally, a network based statistics analysis revealed that DBS attenuated specific couplings that are known to be pathological in PD. Namely, coupling between motor thalamus and sensorimotor cortex was increased and striatal coupling with cerebellum, external pallidum and STN was decreased by DBS.Our results show that rs-fMRI may be acquired in DBS ON and OFF conditions on clinical MRI hardware and that data is useful to gain additional insight into how DBS modulates the functional connectome of the human brain. We demonstrate that effective DBS increases overall connectivity in the motor network, normalizes the network profile toward healthy controls and specifically strengthens thalamo-cortical connectivity while reducing striatal control over basal ganglia and cerebellar structures.


NeuroImage ◽  
2014 ◽  
Vol 90 ◽  
pp. 246-255 ◽  
Author(s):  
Pengfei Xu ◽  
Ruiwang Huang ◽  
Jinhui Wang ◽  
Nicholas T. Van Dam ◽  
Teng Xie ◽  
...  

2017 ◽  
Author(s):  
Stuart J. Ritchie ◽  
Simon R. Cox ◽  
Xueyi Shen ◽  
Michael V. Lombardo ◽  
Lianne M. Reus ◽  
...  

AbstractSex differences in the human brain are of interest, for example because of sex differences in the observed prevalence of psychiatric disorders and in some psychological traits. We report the largest single-sample study of structural and functional sex differences in the human brain (2,750 female, 2,466 male participants; 44-77 years). Males had higher volumes, surface areas, and white matter fractional anisotropy; females had thicker cortices and higher white matter tract complexity. There was considerable distributional overlap between the sexes. Subregional differences were not fully attributable to differences in total volume or height. There was generally greater male variance across structural measures. Functional connectome organization showed stronger connectivity for males in unimodal sensorimotor cortices, and stronger connectivity for females in the default mode network. This large-scale study provides a foundation for attempts to understand the causes and consequences of sex differences in adult brain structure and function.


Author(s):  
Antonio G. Zippo ◽  
Isabella Castiglioni ◽  
Jianyi Lin ◽  
Virginia M. Borsa ◽  
Maurizio Valente ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Jiao Li ◽  
Heng Chen ◽  
Feiyang Fan ◽  
Jiang Qiu ◽  
Lian Du ◽  
...  

Abstract Aberrant topological organization of brain connectomes underlies pathological mechanisms in major depressive disorder (MDD). However, accumulating evidence has only focused on functional organization in brain gray-matter, ignoring functional information in white-matter (WM) that has been confirmed to have reliable and stable topological organizations. The present study aimed to characterize the functional pattern disruptions of MDD from a new perspective—WM functional connectome topological organization. A case-control, cross-sectional resting-state functional magnetic resonance imaging study was conducted on both discovery [91 unmedicated MDD patients, and 225 healthy controls (HCs)], and replication samples (34 unmedicated MDD patients, and 25 HCs). The WM functional networks were constructed in 128 anatomical regions, and their global topological properties (e.g., small-worldness) were analyzed using graph theory-based approaches. At the system-level, ubiquitous small-worldness architecture and local information-processing capacity were detectable in unmedicated MDD patients but were less salient than in HCs, implying a shift toward randomization in MDD WM functional connectomes. Consistent results were replicated in an independent sample. For clinical applications, small-world topology of WM functional connectome showed a predictive effect on disease severity (Hamilton Depression Rating Scale) in discovery sample (r = 0.34, p = 0.001). Furthermore, the topologically-based classification model could be generalized to discriminate MDD patients from HCs in replication sample (accuracy, 76%; sensitivity, 74%; specificity, 80%). Our results highlight a reproducible topologically shifted WM functional connectome structure and provide possible clinical applications involving an optimal small-world topology as a potential neuromarker for the classification and prediction of MDD patients.


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