A multi-shell multi-tissue diffusion study of brain connectivity in early multiple sclerosis
Articolo
Data di Pubblicazione:
2019
Abstract:
Background: The potential of multi-shell diffusion imaging to produce accurate brain connectivity metrics able to unravel key pathophysiological processes in multiple sclerosis (MS) has scarcely been investigated. Objective: To test, in patients with a clinically isolated syndrome (CIS), whether multi-shell imaging-derived connectivity metrics can differentiate patients from controls, correlate with clinical measures, and perform better than metrics obtained with conventional single-shell protocols. Methods: Nineteen patients within 3 months from the CIS and 12 healthy controls underwent anatomical and 53-direction multi-shell diffusion-weighted 3T images. Patients were cognitively assessed. Voxel-wise fibre orientation distribution functions were estimated and used to obtain network metrics. These were also calculated using a conventional single-shell diffusion protocol. Through linear regression, we obtained effect sizes and standardised regression coefficients. Results: Patients had lower mean nodal strength (p = 0.003) and greater network modularity than controls (p = 0.045). Greater modularity was associated with worse cognitive performance in patients, even after accounting for lesion load (p = 0.002). Multi-shell-derived metrics outperformed single-shell-derived ones. Conclusion: Connectivity-based nodal strength and network modularity are abnormal in the CIS. Furthermore, the increased network modularity observed in patients, indicating microstructural damage, is clinically relevant. Connectivity analyses based on multi-shell imaging can detect potentially relevant network changes in early MS.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
clinically isolated syndrome; Diffusion-weighted imaging; multi-shell acquisitions; multi-shell multi-tissue constrained spherical deconvolution; multiple sclerosis; tractography
Elenco autori:
Tur, C.; Grussu, F.; Prados, F.; Charalambous, T.; Collorone, S.; Kanber, B.; Cawley, N.; Altmann, D. R.; Ourselin, S.; Barkhof, F.; Clayden, J. D.; Toosy, A. T.; Wheeler-Kingshott, C.; Ciccarelli, O.
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