During the pre-clinical stages of Alzheimer’s disease, i.e. when subtle changes are taking place in the brain but no cognitive symptoms can be observed, the cortex presents a state of transient hyperexcitability. To date, several studies conducted in animals have shown that tau and beta-amyloid proteins—central to the development of Alzheimer’s disease—were associated with increased cortical excitability and dysfunction of brain networks. However, the relationship between the accumulation of Alzheimer’s disease-related proteins and cortical hyperexcitability during the earliest stages of the disease remains poorly understood in humans, in particular due to technological limitations in the precise quantification of early protein deposition.
A study, conducted by researchers from the Cyclotron Research Centre (CRC In vivo Imaging / GIGA) of ULiège studied whether the first deposits of tau and beta-amyloid proteins in the brains of healthy individuals aged between 50 and 70 years old could be linked to a higher level of cortical excitability. To do this, we combined different neuroimaging methodologies (magnetic resonance imaging, positron emission tomography) in order to characterize the quantity of tau and beta-amyloid proteins in their first agglomeration regions,” explains Gilles Vandewalle, head of the laboratory. That is to say, respectively, in the brainstem and in a series of upper cortical areas. “In addition, the researchers also measured the excitability of the participants’ cortex in a non-invasive manner, using transcranial magnetic stimulation techniques in conjunction with the acquisition of electroencephalographic recordings.
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