|Title||Accumulation of amyloid-β in the cerebellar cortex of essential tremor patients.|
|Publication Type||Journal Article|
|Year of Publication||2015|
|Auteurs||Béliveau, E, Tremblay, C, Aubry-Lafontaine, É, Paris-Robidas, S, Delay, C, Robinson, C, Ferguson, L, Rajput, AH, Rajput, A, Calon, F|
|Date Published||2015 Oct|
|Keywords||Aged, Aged, 80 and over, Alzheimer Disease, Amyloid beta-Peptides, Amyloid beta-Protein Precursor, Apolipoprotein E4, Cerebellar Cortex, Essential Tremor, Female, Humans, Male, Membrane Proteins, Nerve Tissue Proteins, Neurofilament Proteins, Parietal Lobe, Parkinson Disease, Peptide Fragments, Phosphorylation, Purkinje Cells, tau Proteins, Temporal Lobe|
The accumulation of insoluble amyloid-beta (Aβ) peptides is associated with neurodegenerative disorders, such as Alzheimer's disease (AD). As essential tremor (ET) could involve neurodegenerative processes in the cerebellum, we quantified soluble and insoluble Aβ in cerebellar cortices from patients diagnosed with ET (n=9), compared to Controls (n=16) or individuals with Parkinson's disease (n=10). Although ante-mortem cognitive performance was not documented, all individuals included had the diagnosis of AD ruled out by a neuropathologist. ELISA-determined concentrations of insoluble Aβ42 in ET patients displayed a bimodal distribution, with a median 246-fold higher than in Controls (P<0.01, Kruskal-Wallis). Higher Aβ42 concentrations were measured in the parietal cortex of the same ET patients, compared to Controls (107-fold median increase, P<0.01, Kruskal-Wallis), but similar phosphorylated tau levels were detected. The rise in cerebellar insoluble Aβ42 concentrations is not associated to APP expression and processing or the ApoE4 status. However, Aβ42 levels in ET individuals were correlated with cerebellar insoluble phosphorylated tau (r(2)=0.71, P=0.005), unphosphorylated neurofilament heavy chain (NF-H; r(2)=0.50, P=0.030) and Lingo-1 (r(2)=0.73, P=0.007), indicative of a generalized neurodegenerative process involving the cerebellum. Our results suggest prevalent accumulations of insoluble Aβ42 in the cerebellum of ET, but not in age-matched PD. Whether this anomaly plays a role in ET symptoms warrants further investigations.
|Alternate Journal||Neurobiol. Dis.|