Altered brain structural and functional connectivity in schizotypy

2020 ◽  
pp. 1-10
Author(s):  
Yong-ming Wang ◽  
Xin-lu Cai ◽  
Rui-ting Zhang ◽  
Yi-jing Zhang ◽  
Han-yu Zhou ◽  
...  

Abstract Background Schizotypy refers to schizophrenia-like traits below the clinical threshold in the general population. The pathological development of schizophrenia has been postulated to evolve from the initial coexistence of ‘brain disconnection’ and ‘brain connectivity compensation’ to ‘brain connectivity decompensation’. Methods In this study, we examined the brain connectivity changes associated with schizotypy by combining brain white matter structural connectivity, static and dynamic functional connectivity analysis of diffusion tensor imaging data and resting-state functional magnetic resonance imaging data. A total of 87 participants with a high level of schizotypal traits and 122 control participants completed the experiment. Group differences in whole-brain white matter structural connectivity probability, static mean functional connectivity strength, dynamic functional connectivity variability and stability among 264 brain sub-regions of interests were investigated. Results We found that individuals with high schizotypy exhibited increased structural connectivity probability within the task control network and within the default mode network; increased variability and decreased stability of functional connectivity within the default mode network and between the auditory network and the subcortical network; and decreased static mean functional connectivity strength mainly associated with the sensorimotor network, the default mode network and the task control network. Conclusions These findings highlight the specific changes in brain connectivity associated with schizotypy and indicate that both decompensatory and compensatory changes in structural connectivity within the default mode network and the task control network in the context of whole-brain functional disconnection may be an important neurobiological correlate in individuals with high schizotypy.

2016 ◽  
Vol 33 (S1) ◽  
pp. S357-S357 ◽  
Author(s):  
V. Pereira ◽  
P. de Castro-Manglano ◽  
C. Soutullo Esperon

IntroductionAttention deficit hyperactivity disorder (ADHD) is a challenge in child and adolescent psychiatry. In the recent decades many studies with longitudinal designs have used neuroimaging with ADHD patients, suggesting its neurodevelopmental origin.ObjectivesStudy the findings of neuroimaging (MRI, fMRI, DTI, PET) techniques on ADHD patients from a longitudinal point of view, looking also for the potential influence of treatments and other predictors (i.e. genetics).AimsTo provide a global perspective of all the recent findings on ADHD patients with the neuroimaging technics, focusing on longitudinal measurements of the changes in brain development.MethodsWe conducted a review of the literature in the databases Pubmed and ScienceDirect (terms ADHD, neuroimaging, MRI, fMRI, DTI, PET, functional connectivity, metilphenidate and cortical thickness). We focused on studies using neuroimaging techniques with ADHD patients, looking at their populations, methodologies and results.ResultsThe studies found abnormalities in the structure of grey matter, activity and brain connectivity in many neural networks, with particular involvement of the fronto-parietal and Default Mode Network. There is also convergent evidence for white matter pathology and disrupted anatomical connectivity in ADHD. In addition, dysfunctional connectivity during rest and during cognitive tasks has been demonstrated.ConclusionsThis evidence describe ADHD as a brain development disorder, with delays and disruptions in the global development of the central nervous system that compromises grey and white matters, most evident in the prefrontal cortex, parietal and posterior cingulate cortices, as well as basal ganglia, damaging activity and structural and functional connectivity of various brain networks, especially the fronto-striato-parietal and default mode network.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Emiliano Santarnecchi ◽  
Chiara Del Bianco ◽  
Isabella Sicilia ◽  
Davide Momi ◽  
Giorgio Di Lorenzo ◽  
...  

Insomnia might occur as result of increased cognitive and physiological arousal caused by acute or long acting stressors and associated cognitive rumination. This might lead to alterations in brain connectivity patterns as those captured by functional connectivity fMRI analysis, leading to potential insight about primary insomnia (PI) pathophysiology as well as the impact of long-term exposure to sleep deprivation. We investigated changes of voxel-wise connectivity patterns in a sample of 17 drug-naïve PI patients and 17 age-gender matched healthy controls, as well as the relationship between brain connectivity and age of onset, illness duration, and severity. Results showed a significant increase in resting-state functional connectivity of the bilateral visual cortex in PI patients, associated with decreased connectivity between the visual cortex and bilateral temporal pole. Regression with clinical scores originally unveiled a pattern of increased local connectivity as measured by intrinsic connectivity contrast (ICC), specifically resembling the default mode network (DMN). Additionally, age of onset was found to be correlated with the connectivity of supplementary motor area (SMA), and the strength of DMN←→SMA connectivity was significantly correlated with both age of onset (R2 = 41%) and disease duration (R2 = 21%). Chronic sleep deprivation, but most importantly early insomnia onset, seems to have a significant disruptive effect over the physiological negative correlation between DMN and SMA, a well-known fMRI marker of attention performance in humans. This suggests the need for more in-depth investigations on the prevention and treatment of connectivity changes and associated cognitive and psychological deficits in PI patients.


2012 ◽  
Vol 139 (1) ◽  
pp. 56-65 ◽  
Author(s):  
George S. Alexopoulos ◽  
Matthew J. Hoptman ◽  
Dora Kanellopoulos ◽  
Christopher F. Murphy ◽  
Kelvin O. Lim ◽  
...  

2013 ◽  
Author(s):  
Xin Di ◽  
Bharat B. Biswal

Communications between different brain systems are critical to support complex brain functions. Unlike generally high functional connectivity between brain regions from same system, functional connectivity between regions from different systems are more variable. In the present study, we examined whether the connectivity between different brain networks were modulated by other regions by using physiophysiological interaction (PPI) on resting-state functional magnetic resonance imaging data. Spatial independent component analysis was first conducted to identify the default mode network (DMN) and several task positive networks, including the salience, dorsal attention, left and right executive networks. PPI analysis was conducted between pairs of these networks to identify networks or regions that showed modulatory interactions with the two networks. Network-wise analysis revealed reciprocal modulatory interactions between the DMN, salience, and executive networks. Together with the anatomical properties of the salience network regions, the results suggest that the salience network may modulate the relationship between the DMN and executive networks. In addition, voxel-wise analysis demonstrated that the basal ganglia and thalamus positively interacted with the salience network and the dorsal attention network, and negatively interacted with the salience network and the DMN. The results demonstrated complex relationships among brain networks in resting-state, and suggested that between network communications of these networks may be modulated by some critical brain structures such as the salience network, basal ganglia, and thalamus.


2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Matteo De Marco ◽  
Riccardo Manca ◽  
Micaela Mitolo ◽  
Annalena Venneri

White matter hyperintensities (WMHs) are acquired lesions that accumulate and disrupt neuron-to-neuron connectivity. We tested the associations between WMH load and (1) regional grey matter volumes and (2) functional connectivity of resting-state networks, in a sample of 51 healthy adults. Specifically, we focused on the positive associations (more damage, more volume/connectivity) to investigate a potential route of adaptive plasticity. WMHs were quantified with an automated procedure. Voxel-based morphometry was carried out to model grey matter. An independent component analysis was run to extract the anterior and posterior default-mode network, the salience network, the left and right frontoparietal networks, and the visual network. Each model was corrected for age, global levels of atrophy, and indices of brain and cognitive reserve. Positive associations were found with morphometry and functional connectivity of the anterior default-mode network and salience network. Within the anterior default-mode network, an association was found in the left mediotemporal-limbic complex. Within the salience network, an association was found in the right parietal cortex. The findings support the suggestion that, even in the absence of overt disease, the brain actuates a compensatory (neuroplastic) response to the accumulation of WMH, leading to increases in regional grey matter and modified functional connectivity.


2019 ◽  
Author(s):  
Hanna Lu ◽  
Suk Ling Ma ◽  
Winnie Chu Chiu Wing ◽  
Savio Wai Ho Wong ◽  
Linda C. W. Lam

ABSTRACTBackgroundDisturbance of intrinsic brain networks is often associated with APOE ε 4 allele and cognitive dysfunction. However, little is known about the functional connectivity strength (FCS) within default mode network (DMN).ObjectiveWe aimed to examine the independent effects APOE ε 4 and cognitive status and the interaction effect on the functional connectivity within DMN.MethodsResting-state functional MRI was conducted for sixty-five senior adults who had normal cognition or cognitive decline with or without APOE ε 4. Regions within DMN include mPFC, IPL, LTC, hippocampus and PCC. The absolute values of correlation coefficient between DMN regions were employed as the measures of FCS for quantifying the functional connectivity.ResultsMain effect of APOE ε 4 was found on the FCS of bilateral PCC (F = 6.133, p = 0.016), while the main effect of cognitive status was found on the FCS of left IPL and right mPFC (F = 4.585, p = 0.036). Interaction effect was found in the FCS of right mPFC and left LTC (F = 4.698, p = 0.034), right hippocampus and left LTC (F = 7.673, p = 0.008), left PCC and left LTC (F = 6.719, p = 0.012), right IPL and right LTC (F = 4.516, p = 0.038).ConclusionsAPOE ε 4 carriers with cognitive impairment denote a preclinical status characterized by aberrant inter-hemispheric FC within DMN. The network-level connectivity may be useful in the evaluation of the individuals at risk for developing AD and affiliate network-guided brain stimulation.


Author(s):  
Yunlong Nie ◽  
Eugene Opoku ◽  
Laila Yasmin ◽  
Yin Song ◽  
Jie Wang ◽  
...  

AbstractWe conduct an imaging genetics study to explore how effective brain connectivity in the default mode network (DMN) may be related to genetics within the context of Alzheimer’s disease and mild cognitive impairment. We develop an analysis of longitudinal resting-state functional magnetic resonance imaging (rs-fMRI) and genetic data obtained from a sample of 111 subjects with a total of 319 rs-fMRI scans from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. A Dynamic Causal Model (DCM) is fit to the rs-fMRI scans to estimate effective brain connectivity within the DMN and related to a set of single nucleotide polymorphisms (SNPs) contained in an empirical disease-constrained set which is obtained out-of-sample from 663 ADNI subjects having only genome-wide data. We relate longitudinal effective brain connectivity estimated using spectral DCM to SNPs using both linear mixed effect (LME) models as well as function-on-scalar regression (FSR). In both cases we implement a parametric bootstrap for testing SNP coefficients and make comparisons with p-values obtained from asymptotic null distributions. In both networks at an initial q-value threshold of 0.1 no effects are found. We report on exploratory patterns of associations with relatively high ranks that exhibit stability to the differing assumptions made by both FSR and LME.


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