PET Study of Microglial Activation in Kleine-Levin Syndrome

克莱恩-莱文综合征小胶质细胞活化的 PET 研究

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作者:Lucie Barateau, Anis Krache, Alexandre Da Costa, Michel Lecendreux, Sofiene Chenini, Nicolas Arlicot, Patrick Vourc'h, Mathieu Alonso, Anne-Sophie Salabert, Séverine Beziat, Isabelle Jaussent, Denis Mariano-Goulart, Pierre Payoux, Yves Dauvilliers

Discussion

Our findings do not support the presence of neuroinflammation in KLS. Further research is needed to identify relevant biomarkers in KLS.

Methods

Patients with KLS and controls underwent a standardized clinical evaluation and PET imaging, using a radiolabeled ligand specific to the 18 kDa translocator protein. Images were processed on the PMOD (peripheral module) interface using a standard uptake value (SUV). Five regions of interest (ROIs) were analyzed: hypothalamus, thalamus, frontal area, cerebellum, and whole brain. SUV ratios (SUVr) were calculated by normalizing SUV with cerebellum uptake.

Results

Images of 17 consecutive patients with KLS (7 during episodes, 10 out of episodes) and 14 controls were analyzed. We found no SUV/SUVr difference between KLS and controls, between patients in and out episodes in all ROIs, and no correlation between SUVr and episode duration at the time of PET scan. No association was found between SUVr and sex, disease duration, or orexin levels.

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