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Molecular Imaging of Microglial Activation in Amyotrophic Lateral Sclerosis
Author(s) -
Philippe Corcia,
Clovis Tauber,
Johnnie Vercoullie,
Nicolas Arlicot,
Caroline Prunier,
Julien Praline,
Nicolas Guillaume,
Y. Venel,
Caroline Hommet,
JeanLouis Baulieu,
JeanPhilippe Cottier,
Catherine Roussel,
Michael Kassiou,
Denis Guilloteau,
Maria-Joao Santiago Ribeiro
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0052941
Subject(s) - amyotrophic lateral sclerosis , microglia , neuroscience , medicine , biology , pathology , immunology , inflammation , disease
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, 18 F-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 18 F-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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