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Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...

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Imaging chronic active lesions in multiple sclerosis: a consensus statement.

Francesca Bagnato1,2, Pascal Sati3, Christopher C Hemond4

  • 1Neuroimaging Unit, Neuroimmunology Division, Department of Neurology, Vanderbilt University Medical Center, Nashville, TN 37212, USA.

Brain : a Journal of Neurology
|January 16, 2024
PubMed
Summary
This summary is machine-generated.

New imaging biomarkers can detect chronic active lesions (CAL) in multiple sclerosis (MS) brains. A consensus statement provides guidance for their radiological definition and measurement to aid clinical translation.

Keywords:
MRI-defined slowly evolving lesionschronic active lesionsironmicrogliamultiple sclerosisparamagnetic rim lesions

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Area of Science:

  • Neuroimaging
  • Neurology
  • Inflammation research

Background:

  • Chronic active lesions (CAL) are key indicators of chronic inflammation in multiple sclerosis (MS), impacting disease progression.
  • Recent advancements in MRI and PET imaging allow for in vivo detection and quantification of CAL in MS patients.

Purpose of the Study:

  • To present a consensus statement from the North American Imaging in Multiple Sclerosis Cooperative on the radiological definition and measurement of CAL.
  • To summarize the development process of this consensus statement and highlight existing knowledge gaps.

Main Methods:

  • Review of innovative MRI and PET-derived biomarkers for CAL detection, including paramagnetic rim lesions and 18-kDa translocator protein-positive lesions.
  • Development of a consensus statement providing radiological guidance for CAL identification, quantification, and monitoring.

Main Results:

  • Identification of promising candidate biomarkers for CAL, such as paramagnetic rim lesions and slowly expanding lesions on MRI, and 18-kDa translocator protein-positive lesions on PET.
  • Acknowledgement that current biomarkers have overlapping but not equivalent sensitivity and specificity compared to histopathological CAL.
  • Highlighting the lack of standardization in current imaging measures for CAL.

Conclusions:

  • The consensus statement offers crucial guidance for standardizing CAL assessment in MS.
  • Further research is needed to address remaining knowledge gaps and refine imaging biomarkers for more accurate CAL detection and monitoring.