Published December 31, 2012 | Version v1
Journal article Open

Molecular Imaging of Microglial Activation in Amyotrophic Lateral Sclerosis

  • 1. ALS Center, Department of Neurology, CHRU Bretonneau, Tours, France; Universite´ Franc¸ois Rabelais de Tours, Tours, France and Inserm U 930, Tours, France
  • 2. Universite´ Franc¸ois Rabelais de Tours, Tours, France, and Inserm U 930, Tours, France
  • 3. Universite´ Franc¸ois Rabelais de Tours, Tours, France; Inserm U 930, Tours, France and Nuclear Medicine Department, CHRU Tours, France
  • 4. Nuclear Medicine Department, CHRU Tours, France
  • 5. ALS Center, Department of Neurology, CHRU Bretonneau, Tours, France
  • 6. ALS Center, Department of Neurology, CHRU Angers, Angers, France
  • 7. Universite´ Franc¸ois Rabelais de Tours, Tours, France and Inserm U 930, Tours, France
  • 8. CIC-IT 806 Ultrasons et Radiopharmaceutiques, Tours, France
  • 9. School of Chemistry, University of Sydney, New South Wales, Australia; Brain and Mind Research Institute, Sydney, New South Wales, Australia and Discipline of Med Rad Sci, Univ Sydney, New South, Wales, Australia
  • 10. Universite´ Franc¸ois Rabelais de Tours, Tours, France; Inserm U 930, Tours, France; Nuclear Medicine Department, CHRU Tours, France and CIC-IT 806 Ultrasons et Radiopharmaceutiques, Tours, France

Description

There is growing evidence of activated microglia and inflammatory processes in the cerebral cortex in amyotrophic lateral sclerosis (ALS). Activated microglia is characterized by increased expression of the 18 kDa translocator protein (TSPO) in the brain and may be a useful biomarker of inflammation. In this study, we evaluated neuroinflammation in ALS patients using a radioligand of TSPO, 18F-DPA-714. Ten patients with probable or definite ALS (all right-handed, without dementia, and untreated by riluzole or other medication that might bias the binding on the TSPO), were enrolled prospectively and eight healthy controls matched for age underwent a PET study. Comparison of the distribution volume ratios between both groups were performed using a Mann-Whitney’s test. Significant increase of distribution of volume ratios values corresponding to microglial activation was found in the ALS sample in primary motor, supplementary motor and temporal cortex (p = 0.009, p = 0.001 and p = 0.004, respectively). These results suggested that the cortical uptake of 18F-DPA-714 was increased in ALS patients during the ‘‘time of diagnosis’’ phase of the disease. This finding might improve our understanding of the pathophysiology of ALS and might be a surrogate marker of efficacy of treatment on microglial activation.

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Funding

INMIND – Imaging of Neuroinflammation in Neurodegenerative Diseases 278850
European Commission