scholarly journals Fronto-limbic dysconnectivity leads to impaired brain network controllability in young people with bipolar disorder and those at high genetic risk

2017 ◽  
Author(s):  
Jayson Jeganathan ◽  
Alistair Perry ◽  
Danielle S. Bassett ◽  
Gloria Roberts ◽  
Philip B. Mitchell ◽  
...  

AbstractRecent investigations have used diffusion-weighted imaging to reveal disturbances in the neurocircuitry that underlie cognitive-emotional control in bipolar disorder (BD) and in unaffected siblings or children at high genetic risk (HR). It has been difficult to quantify the mechanism by which structural changes disrupt the superimposed brain dynamics, leading to the emotional lability that is characteristic of BD. Average controllability is a concept from network control theory that extends structural connectivity data to estimate the manner in which local neuronal fluctuations spread from a node or subnetwork to alter the state of the rest of the brain. We used this theory to ask whether structural connectivity deficits previously observed in HR (n=84, mean age 22.4) individuals, patients with BD (n=38, mean age 23.9), and age- and gender-matched controls (n=96, mean age 22.6) translate to differences in the ability of brain systems to be manipulated between states. Localized impairments in network controllability were seen in the left parahippocampal, left middle occipital, left superior frontal, right inferior frontal, and right precentral gyri in BD and HR groups. Subjects with BD had distributed deficits in a subnetwork containing the left superior and inferior frontal gyri, postcentral gyrus, and insula (p=0.004). HR participants had controllability deficits in a right-lateralized subnetwork involving connections between the dorsomedial and ventrolateral prefrontal cortex, the superior temporal pole, putamen, and caudate nucleus (p=0.008). Between-group controllability differences were attenuated after removal of topological factors by network randomization. Some previously reported differences in network connectivity were not associated with controllability-differences, likely reflecting the contribution of more complex brain network properties. These analyses highlight the potential functional consequences of altered brain networks in BD, and may guide future clinical interventions.HighlightsControl theory estimates how neuronal fluctuations spread from local networks.We compare brain controllability in bipolar disorder and their high-risk relatives.These groups have impaired controllability in networks supporting cognitive and emotional control.Weaker connectivity as well as topological alterations contribute to these changes.

2018 ◽  
Vol 19 ◽  
pp. 71-81 ◽  
Author(s):  
Jayson Jeganathan ◽  
Alistair Perry ◽  
Danielle S. Bassett ◽  
Gloria Roberts ◽  
Philip B. Mitchell ◽  
...  

2019 ◽  
Vol 245 ◽  
pp. 228-236 ◽  
Author(s):  
Riya Wadhwa ◽  
Wei Wen ◽  
Andrew Frankland ◽  
Vivian Leung ◽  
Carina Sinbandhit ◽  
...  

Author(s):  
Linden Parkes ◽  
Tyler M. Moore ◽  
Monica E. Calkins ◽  
Matthew Cieslak ◽  
David R. Roalf ◽  
...  

ABSTRACTBackgroundThe psychosis spectrum is associated with structural dysconnectivity concentrated in transmodal association cortex. However, understanding of this pathophysiology has been limited by an exclusive focus on the direct connections to a region. Using Network Control Theory, we measured variation in both direct and indirect structural connections to a region to gain new insights into the pathophysiology of the psychosis spectrum.MethodsWe used psychosis symptom data and structural connectivity in 1,068 youths aged 8 to 22 years from the Philadelphia Neurodevelopmental Cohort. Applying a Network Control Theory metric called average controllability, we estimated each brain region’s capacity to leverage its direct and indirect structural connections to control linear brain dynamics. Next, using non-linear regression, we determined the accuracy with which average controllability could predict negative and positive psychosis spectrum symptoms in out-of-sample testing. We also compared prediction performance for average controllability versus strength, which indexes only direct connections to a region. Finally, we assessed how the prediction performance for psychosis spectrum symptoms varied over the functional hierarchy spanning unimodal to transmodal cortex.ResultsAverage controllability outperformed strength at predicting positive psychosis spectrum symptoms, demonstrating that indexing indirect structural connections to a region improved prediction performance. Critically, improved prediction was concentrated in association cortex for average controllability, whereas prediction performance for strength was uniform across the cortex, suggesting that indexing indirect connections is crucial in association cortex.ConclusionsExamining inter-individual variation in direct and indirect structural connections to association cortex is crucial for accurate prediction of positive psychosis spectrum symptoms.


2019 ◽  
Vol 29 ◽  
pp. S129
Author(s):  
Philip Mitchell ◽  
Gloria Roberts ◽  
Rhoshel K. Lenroot ◽  
Bronwyn Overs ◽  
Janice Fullerton ◽  
...  

2017 ◽  
Vol 81 (10) ◽  
pp. S318-S319 ◽  
Author(s):  
Philip Mitchell ◽  
Michael Breakspear ◽  
Gloria Roberts ◽  
Alistair Perry ◽  
Andrew Frankland ◽  
...  

2016 ◽  
Vol 33 (S1) ◽  
pp. S124-S125
Author(s):  
M.R. Raposo ◽  
M.D. Piqueras ◽  
I. Martínez ◽  
A.L. Galdámez ◽  
A. Gil ◽  
...  

IntroductionAlthough early interventions in individuals with bipolar disorder may reduce the associated personal and economic burden, the neurobiologic markers of enhanced risk are unknown.ObjectivesThe objective of this paper is to analyze the existence of neurobiological abnormalities in individuals with genetic risk for developing bipolar disorder (HR)Material and methodsA literature search was performed in the available scientific literature on the subject study object, by searching MEDLINE.ResultsThere were 37 studies included in this systematic review. The overall sample for the systematic review included 1258 controls and 996 HR individuals. No significant differences were detected between HR individuals and controls in the selected ROIs (regions of interest): striatum, amygdala, hippocampus, pituitary and frontal lobe. The HR group showed increased grey matter volume compared with patients with established bipolar disorder. The HR individuals showed increased neural response in the left superior frontal gyrus, medial frontal gyrus and left insula compared with controls. The overall results found no significant differences between individuals at high genetic risk and controls since the magnitude of the association as corresponds to an OR < 1.5 (low association)ConclusionThere is accumulating evidence for the existence of neurobiologic abnormalities in individuals at genetic risk for bipolar disorder at various scales of investigation. The etiopathogenesis of bipolar disorder will be better elucidated by future imaging studies investigating larger and more homogeneous samples and using longitudinal designs to dissect neurobiologic abnormalities that are underlying traits of the illness from those related to psychopathologic states, such as episodes of mood exacerbation or pharmacologic treatment.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2012 ◽  
Vol 37 (12) ◽  
pp. 2720-2729 ◽  
Author(s):  
Heather C Whalley ◽  
Martina Papmeyer ◽  
Liana Romaniuk ◽  
Emma Sprooten ◽  
Eve C Johnstone ◽  
...  

2016 ◽  
Vol 23 (2) ◽  
pp. 413-421 ◽  
Author(s):  
G Roberts ◽  
A Perry ◽  
A Lord ◽  
A Frankland ◽  
V Leung ◽  
...  

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