Evidence of diffuse cerebellar neuroinflammation in multiple sclerosis by 11C-PBR28 MR-PET

Mult Scler. 2020 May;26(6):668-678. doi: 10.1177/1352458519843048. Epub 2019 Apr 11.

Abstract

Background: Activated microglia, which can be detected in vivo by 11C-PBR28 positron emission tomography (PET), represent a main component of MS pathology in the brain. Their role in the cerebellum is still unexplored, although cerebellar involvement in MS is frequent and accounts for disability progression.

Objectives: We aimed at characterizing cerebellar neuroinflammation in MS patients compared to healthy subjects by combining 11C-PBR28 MRI-Positron Emission Tomography (MR-PET) with 7 Tesla (T) MRI and assessing its relationship with brain neuroinflammation and clinical outcome measures.

Methods: Twenty-eight MS patients and 16 healthy controls underwent 11C-PBR28 MR-PET to measure microglia activation in normal appearing cerebellum and lesions segmented from 7 T scans. Patients were evaluated using the Expanded Disability Status Scale and Symbol Digit Modalities Test. 11C-PBR28 binding was assessed in regions of interest using 60-90 minutes standardized uptake values normalized by a pseudo-reference region in the brain normal appearing white matter. Multilinear regression was used to compare tracer uptake in MS and healthy controls and assess correlations with clinical scores.

Results: In all cerebellar regions examined, MS patients showed abnormally increased tracer uptake, which correlated with cognitive and neurological disability.

Conclusion: Neuroinflammation is widespread in the cerebellum of patients with MS and related to neurological disability and cognitive impairment.

Keywords: Cerebellum; MR-PET; microglia; neuroinflammation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Cerebellum* / diagnostic imaging
  • Cerebellum* / immunology
  • Cerebellum* / metabolism
  • Cerebellum* / pathology
  • Female
  • Humans
  • Inflammation* / diagnostic imaging
  • Inflammation* / immunology
  • Inflammation* / metabolism
  • Inflammation* / pathology
  • Magnetic Resonance Imaging
  • Male
  • Microglia*
  • Middle Aged
  • Multimodal Imaging
  • Multiple Sclerosis* / diagnostic imaging
  • Multiple Sclerosis* / immunology
  • Multiple Sclerosis* / metabolism
  • Multiple Sclerosis* / pathology
  • Neuroimaging*
  • Positron-Emission Tomography
  • Pyrimidines / pharmacokinetics*
  • White Matter* / diagnostic imaging
  • White Matter* / immunology
  • White Matter* / metabolism
  • White Matter* / pathology

Substances

  • (methyl-(11)C)N-acetyl-N-(2-methoxybenzyl)-2-phenoxy-5-pyridinamine
  • Pyrimidines