Abstract

BackgroundMore than 80% of multiple sclerosis (MS) patients experience symptoms of fatigue. MS-related fatigue is only partly explained by structural (lesions and atrophy) and functional (brain activation and conventional static functional connectivity) brain properties. ObjectivesTo investigate the relationship of dynamic functional connectivity (dFC) with fatigue in MS patients and to compare dFC with commonly used clinical and MRI parameters. MethodsIn 35 relapsing-remitting MS patients (age: 42.83 years, female/male: 20/15, disease duration: 11 years) and 19 healthy controls (HCs) (age: 41.38 years, female/male: 11/8), fatigue was measured using the CIS-20r questionnaire at baseline and at 6-month follow-up. All subjects underwent structural and resting-state functional MRI at baseline. Global static functional connectivity (sFC) and dynamic functional connectivity (dFC) were calculated. dFC was assessed using a sliding-window approach by calculating the summed difference (diff) and coefficient of variation (cv) across windows. Moreover, regional connectivity between regions previously associated with fatigue in MS was estimated (i.e. basal ganglia and regions of the Default Mode Network (DMN): medial prefrontal, posterior cingulate and precuneal cortices). Hierarchical regression analyses were performed with forward selection to identify the most important correlates of fatigue at baseline. Results were not corrected for multiple testing due to the exploratory nature of the study. ResultsPatients were more fatigued than HCs at baseline (p = 0.001) and follow-up (p = 0.002) and fatigue in patients was stable over time (p = 0.213). Patients had significantly higher baseline global dFC than HCs, but no difference in basal ganglia-DMN dFC. In the regression model for baseline fatigue in patients, basal ganglia-DMN dFC-cv (standardized β = -0.353) explained 12.5% additional variance on top of EDSS (p = 0.032). Post-hoc analysis revealed higher basal ganglia-DMN dFC-cv in non-fatigued patients compared to healthy controls (p = 0.013), whereas fatigued patients and healthy controls showed similar basal ganglia-DMN dFC. ConclusionsLess dynamic connectivity between the basal ganglia and the cortex is associated with greater fatigue in MS patients, independent of disability status. Within patients, lower dynamics of these connections could relate to lower efficiency and increased fatigue. Increased dynamics in non-fatigued patients compared to healthy controls might represent a network organization that protects against fatigue or signal early network dysfunction.

Highlights

  • Fatigue is one of the most common symptoms in multiple sclerosis (MS), with up to 83% of patients reporting symptoms of transient or chronic fatigue during the disease course (Manjaly et al, 2019)

  • In line with previous literature describing functional connectivity alterations in MS patients overall, patients in this study showed greater global dynamic functional connectivity (dFC) compared to healthy controls (HCs)

  • Lower dFC of specific connections between the basal ganglia and cortical regions within the Default Mode Network (DMN) relates to greater baseline fatigue in MS pa­ tients

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Summary

Introduction

Fatigue is one of the most common symptoms in multiple sclerosis (MS), with up to 83% of patients reporting symptoms of transient or chronic fatigue during the disease course (Manjaly et al, 2019). Various primary (neuro)biological correlates of fatigue in MS have been described in the literature, though the explanatory value is low Many of these correlates can be fitted into a framework involving physiological alterations in the basal ganglia and frontoparietal regions on various levels of organization. Task-based fMRI studies suggest that dysfunction of frontal cortical regions and basal ganglia relates to fatigue in MS patients (Fil­ ippi et al, 2002; Roelcke et al, 1997). Reductions in fatigue in response to medication correlate with the modification of these functional basal ganglia-cortical connections, further linking the functional brain network to fatigue in MS patients (Rocca et al, 2018). Patients had significantly higher baseline global dFC than HCs, but no difference in basal ganglia-DMN dFC. Increased dynamics in non-fatigued patients compared to healthy controls might represent a network organization that protects against fatigue or signal early network dysfunction

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