Quantification and clinical relevance of brain atrophy in multiple sclerosis: a review

Blandine Grassiot1, Béatrice Desgranges, Francis Eustache

  • 1Département de Neurologie, CHU Côte de Nacre, 14000 Caen, France.

Journal of Neurology
|April 9, 2009
PubMed

Insights

Grey matter atrophy is a key indicator of multiple sclerosis (MS) progression, strongly linked to clinical and cognitive decline. This review details MRI methods for quantifying atrophy and its relevance in MS phenotypes.

Area of Science:

  • Neurology
  • Radiology
  • Neuroscience

Background:

  • Multiple sclerosis (MS) is an inflammatory demyelinating disease.
  • White matter lesions are traditional markers, but cortical lesions and brain atrophy are emerging as critical indicators of disease progression.
  • Magnetic Resonance Imaging (MRI) enables reproducible quantification of brain tissue loss.

Purpose of the Study:

  • To review MRI-based methods for quantifying whole and regional brain atrophy in MS.
  • To discuss the clinical relevance of brain atrophy by examining its relationship with white matter lesions, motor, and cognitive disabilities.
  • To emphasize the role of brain atrophy across different MS phenotypes.

Main Methods:

  • Review of current literature on MRI-based quantification of brain atrophy.
  • Correlation analysis between brain atrophy, white matter lesions, and clinical/cognitive disability.
  • Examination of brain atrophy patterns in various MS phenotypes.

Main Results:

  • Grey matter (GM) atrophy is well-established in MS and significantly associated with clinical and cognitive deterioration.
  • GM volume loss manifests as focal atrophy in deep grey nuclei and diffuse cortical atrophy.
  • Phenotypic variations in MS correlate with different degrees and regional locations of brain atrophy.

Conclusions:

  • Brain atrophy, particularly grey matter atrophy, is a crucial pathological marker in MS progression.
  • MRI quantification of brain atrophy is vital for understanding its association with disability and cognition.
  • Further research is needed to elucidate the specific discrepancies in brain atrophy across different MS forms.