Increased perfusion in normal appearing white matter in high inflammatory multiple sclerosis patients

PLoS One. 2015 Mar 16;10(3):e0119356. doi: 10.1371/journal.pone.0119356. eCollection 2015.

Abstract

Purpose: Although cerebral perfusion alterations have long been acknowledged in multiple sclerosis (MS), the relationship between measurable perfusion changes and the status of highly active MS has not been examined. We hypothesized that alteration of perfusion can be detected in normal appearing white matter and is increased in high inflammatory patients.

Materials and methods: Thirty-three patients with relapsing-remitting MS underwent four monthly 3T MRI scans including dynamic susceptibility contrast perfusion-weighted MRI. Cerebral blood flow (CBF) and cerebral blood volume (CBV) were measured in normal appearing white matter. Patients were stratified in a high- and low-inflammatory group according to the number of new contrast enhancing lesions.

Results: Thirteen patients were classified as high-inflammatory. Compared to low-inflammatory patients, the high-inflammatory group demonstrated significantly higher CBV (p = 0.001) and CBF (p = 0.014) values. A mixed model analysis to assess independent variables associated with CBV and CBF revealed that white matter lesion load and atrophy measurements had no significant influence on CBF and CBV.

Conclusion: This work provides evidence that high inflammatory lesion load is associated with increased CBV and CBF, underlining the role of global modified microcirculation prior to leakage of the blood-brain barrier in the pathophysiology of MS. Perfusion changes might therefore be sensitive to active inflammation apart from lesion development without local blood-brain barrier breakdown, and could be utilized to further assess the metabolic aspect of current inflammation.

MeSH terms

  • Adult
  • Cerebrovascular Circulation*
  • Female
  • Humans
  • Inflammation / diagnosis*
  • Inflammation / physiopathology
  • Magnetic Resonance Angiography
  • Male
  • Middle Aged
  • Multiple Sclerosis, Relapsing-Remitting / physiopathology*
  • Prospective Studies
  • White Matter / blood supply*
  • White Matter / physiopathology
  • Young Adult

Grants and funding

The authors have no support or funding to report.