Disrupted hemodynamic response within dorsolateral prefrontal cortex during cognitive tasks among people with multiple sclerosis-related fatigue

PLoS One. 2024 Jun 5;19(6):e0303211. doi: 10.1371/journal.pone.0303211. eCollection 2024.

Abstract

Introduction: Mental fatigue is an early and enduring symptom in persons with autoimmune disease particularly multiple sclerosis (MS). Neuromodulation has emerged as a potential treatment although optimal cortical targets have yet to be determined. We aimed to examine cortical hemodynamic responses within bilateral dorsolateral prefrontal cortex (dlPFC) and frontopolar areas during single and dual cognitive tasks in persons with MS-related fatigue compared to matched controls.

Methods: We recruited persons (15 MS and 12 age- and sex-matched controls) who did not have physical or cognitive impairment and were free from depressive symptoms. Functional near infrared spectroscopy (fNIRS) registered hemodynamic responses during the tasks. We calculated oxyhemoglobin peak, time-to-peak, coherence between channels (a potential marker of neurovascular coupling) and functional connectivity (z-score).

Results: In MS, dlPFC demonstrated disrupted hemodynamic coherence during both single and dual tasks, as evidenced by non-significant and negative correlations between fNIRS channels. In MS, reduced coherence occurred in left dorsolateral PFC during the single task but occurred bilaterally as the task became more challenging. Functional connectivity was lower during dual compared to single tasks in the right dorsolateral PFC in both groups. Lower z-score was related to greater feelings of fatigue. Peak and time-to-peak hemodynamic response did not differ between groups or tasks.

Conclusions: Hemodynamic responses were inconsistent and disrupted in people with MS experiencing mental fatigue, which worsened as the task became more challenging. Our findings point to dlPFC, but not frontopolar areas, as a potential target for neuromodulation to treat cognitive fatigue.

MeSH terms

  • Adult
  • Case-Control Studies
  • Cognition* / physiology
  • Dorsolateral Prefrontal Cortex* / diagnostic imaging
  • Dorsolateral Prefrontal Cortex* / physiopathology
  • Fatigue / physiopathology
  • Female
  • Hemodynamics*
  • Humans
  • Male
  • Mental Fatigue / physiopathology
  • Middle Aged
  • Multiple Sclerosis* / complications
  • Multiple Sclerosis* / physiopathology
  • Prefrontal Cortex / diagnostic imaging
  • Prefrontal Cortex / physiopathology
  • Spectroscopy, Near-Infrared*

Grants and funding

The research was funded by Canada Research Chairs (Grant Number 2019-00290) and Canada Foundation for Innovation (Grant Number 33621) (MP). The funders were not involved in the conduct of the research.