Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/40092
Conference/Presentation Title: Longitudinal change in structural connectome in Huntington's disease: The image-HD study.
Authors: Chua P.;Stout J.C.;Churchyard A.;Georgiou-Karistianis N. ;Poudel G.;Egan G.F.
Monash Health Department(s): Neurology
Urology
Institution: (Georgiou-Karistianis, Stout, Egan, Poudel) Monash Institute of Cognitive and Clinical Neurosciences, School of Psychological Sciences, Monash University, Clayton, VIC, Australia (Churchyard, Chua) Department of Neurology, Monash Medical Centre, Clayton, VIC, Australia (Egan) Monash Biomedical Imaging (MBI), Monash University, Melbourne, VIC, Australia
Presentation/Conference Date: 14-Aug-2017
Copyright year: 2016
Publisher: BMJ Publishing Group
Publication information: Journal of Neurology, Neurosurgery and Psychiatry. Conference: 2016 Annual Meeting of the European Huntington's Disease Network, EHDN 2016. The Hague Netherlands. 87 (Supplement 1) (pp A38), 2016. Date of Publication: September 2016.
Abstract: Aims To investigate 18 month longitudinal changes in structural connectome in pre-HD and symp-HD, compared with controls. Method Longitudinal analysis of diffusion tensor imaging data was conducted for 28 pre-HD, 25 symp-HD, and 27 controls at baseline and 18 months. Unbiased tensor-based registration pipeline was used to register diffusion tensor data across time and groups. Whole brain probabilistic tractography was performed by seeding 50 million white-matter tracts (streamlines). The SIFT algorithm (spherical-deconvolution informed filtering of tractograms) removed bias in reconstructed tracts. 90x90 structural connectome was generated for each group. Longitudinal change in connectome was analysed using a Network Based Statistics analysis method and a group by time ANOVA model. Results There was a significant within group change in structural connectivity in pre-HD and symp-HD (P < 0.05, FDR Corrected) but not controls. In pre-HD, longitudinal change was observed in two distinct networks: the first connected striatum with motor cortex and the second connected prefrontal cortex with parieto-occipital cortices. In symp-HD, longitudinal change was observed in widespread connexions between frontal and parietal cortices, and striatum and cortex. No distinct networklevel changes were observed in symp-HD. Conclusions Structural connectome analysis can capture network- specific structural disconnectivity. While connectivity change in symp-HD was diffuse overall, the pre-HD group showed distinct networks that changed over time. These connectional pathways offer new avenues to further investigate disease spread pathways in HD.
Conference Start Date: 2016-09-16
Conference End Date: 2016-09-18
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1136/jnnp-2016-314597.111
ISSN: 1468-330X
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/40092
Type: Conference Abstract
Subjects: diffusion tensor imaging
filtration
frontoparietal cortex
*Huntington chorea
motor cortex
occipital cortex
pipeline
prefrontal cortex
registration
statistics
white matter
analysis of variance
*connectome
controlled study
corpus striatum
statistics
white matter
frontoparietal cortex
filtration
diffusion tensor imaging
corpus striatum
*Huntington chorea
*connectome
analysis of variance
controlled study
motor cortex
occipital cortex
pipeline
prefrontal cortex
registration
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