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Dynamic modular-level alterations of structural-functional coupling in clinically isolated syndrome.
Ismail Koubiyr1,2, Pierre Besson3,4, Mathilde Deloire5
1University of Bordeaux, F Bordeaux, France.
In early multiple sclerosis (MS), structural brain damage precedes functional changes, leading to decoupling between structural and functional connectivity. This occurs even with preserved cognitive function, suggesting compensatory mechanisms.
Area of Science:
- Neuroscience
- Radiology
- Neurology
Background:
- Multiple sclerosis (MS) involves abnormalities in brain structure and function.
- The relationship between evolving structural and functional connectivity in MS is not well understood.
- Structural-functional coupling may detect brain alterations more sensitively than individual modalities.
Purpose of the Study:
- To investigate the longitudinal changes in structural-functional coupling in the first year after clinically isolated syndrome (CIS).
- To explore global and modular alterations in connectivity over time.
- To test the hypothesis that MS causes decoupling between functional and structural connectivity.
Main Methods:
- Prospective study of 41 patients with CIS and 19 healthy controls over 1 year.
- Resting-state functional MRI and diffusion tensor imaging at baseline and follow-up.
- Graph theory analysis and neuropsychological assessments.
Main Results:
- Patients with CIS showed baseline structural reorganization (increased clustering coefficient) and modular alterations.
- After 1 year, both structural and functional reorganization occurred, with abnormal modular connectivity and increased functional betweenness centrality.
- Structural-functional decoupling was observed in salience, visual, and somatomotor networks, despite preserved cognitive performance.
Conclusions:
- Structural damage precedes functional reorganization in the first year of MS following CIS.
- The observed structural-functional decoupling suggests compensatory mechanisms are active.
- Functional reorganization may occur via indirect anatomical pathways in early MS.
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