Epilepsy in Alzheimer's Disease: Effect on Disease Progression (EADP)

This is a long-term, prospective, interventional study to investigate the role and prevalence of subclinical epileptiform activity in the hippocampus in patients with mild cognitive impairment (MCI) due to Alzheimer's disease (AD). The investigators would like to investigate whether subclinical epileptiform activity in the hippocampus is more prevalent in patients with MCI, compared to healthy controls and to evaluate its effects on cognitive decline. Evolution of cognitive decline will be assessed over a time period of two years.

Epilepsy is a known comorbidity of Alzheimer's disease. In the past, it was considered to be a late complication of AD. Recent literature suggest seizures to be prevalent much earlier in the time course of the disease. Systematic reviews suggest the occurrence of at least one seizure in 10-22% of AD cases and of epilepsy in 5 out of 100 AD cases. One important factor leading to the underdiagnosis of epilepsy in AD, is the fact that it is difficult to diagnose epilepsy in patients with AD because of an overlap in symptomatology (e.g. speech arrest, staring, confusion, …) A recent pilot study showed that even subclinical epileptiform discharges, without overt epilepsy, were more frequent (42%) in patients with dementia due to AD than in healthy controls (10%). These subclinical epileptic discharges were diagnosed with prolonged electroencephalogram (EEG)-monitoring and magnetoencephalogram (MEG)-registration. There is overlap in AD and epilepsy pathogenesis. In both diseases, activation of microglia, astrogliosis, neuroinflammation and hippocampal neuronal loss has been described. Studies in mice have shown that hippocampal hyperexcitability is an early electrophysiological impairment in AD, and, that this might be a consequence of soluble Amyloid bèta oligomers. Another study in mice, expressing human Amyloid Precursor Protein (APP), showed hippocampal synchronized large amplitude potentials to be present before onset of spontaneous seizures, memory impairments or Amyloid bèta plaques. Low levels of soluble forms of Amyloid bèta might have increased excitability. Increased neuronal activity per se increases both Amyloid bèta and Tau secretion. This means that recurrent epileptic activity in AD might establish a vicious cycle. Since hippocampal hyperactivity might be an early electrophysiological impairment in AD according to rodent studies, even before memory impairment exist, the investigators thought it to be useful to track subclinical, hippocampal epileptic activity by use of magnetoencephalogram - high density electroencephalogram (MEG-EEG) in patients with MCI due to AD (aka a stage of predementia) and compare this prevalence to healthy controls. The investigators would also like to track evolution to AD in patients with MCI and subclinical epileptiform activity versus those without. This could support further investigations, with monitoring of the effect of several antiepileptic drugs in patients with MCI due to AD.

Neuropsychological investigation, lumbar puncture, long term-EEG monitoring and/or MEG-EEG, magnetic resonance imaging (MRI), blood sample with deep genetic profiling and Apolipoprotein E (APOE) determination.

Neuropsychological investigation, lumbar puncture, long term-EEG monitoring and/or MEG-EEG, MRI, blood sample with deep genetic profiling and APOE determination.

Prevalence, expressed as percentage, of subclinical epileptiform activity in MCI due to AD patients, compared to healthy controls.

Patients will have their investigations at inlcusion within a time frame of 8 weeks. Healthy Volunteers will have their investigations at inclusion within a time frame of 4 weeks.

Odds ratio for conversion to clinical AD when comparing MCI patients with and without subclinical signs of epilepsy at the baseline evaluation.

Patients will have their investigations at inlcusion (time frame: 8 weeks), after 1 year (time frame: 4 weeks) and after 2 years (time frame: 4 weeks).

Patients Inclusion Criteria: Cognitive concern reflecting a change in cognition reported by patient or informant or clinician Objective evidence of impairment in one or more cognitive domains, typically including memory. Preservation of independence in functional abilities Not demented Exclusion Criteria: Age < 18 years old Pregnancy Expected death due to illness within 2 years Pacemaker or other ferromagnetic material that is not MRI compatible Other neurodegenerative or cerebrovascular disease Pattern compatible with Normal Pressure Hydrocephalus (NPH) (clinically, imaging) Epilepsy Multiple sclerosis or other demyelinating disease Depression, psychosis or other mental disease Use of anti-epileptic drugs Alcohol or substance abuse Korsakoff syndrome Symptomatic liver disease Uncontrolled thyroid disorders Untreated HIV or syphilis Clinically significant vitamin B12 deficiency Severe systemic medical illness (eg end-stage cardiac disease, …) Healthy volunteers Inclusion criteria Age- and gender matched healthy controls Exclusion criteria Age < 18 years old Pregnancy Pacemaker or other ferromagnetic material that is not MRI compatible Mild cognitive impairment or dementia of any cause Epilepsy Multiple sclerosis or other demyelinating disease Depression, psychosis or other mental disease Use of anti-epileptic drugs Alcohol or substance abuse Symptomatic liver disease Uncontrolled thyroid disorders Untreated HIV or syphilis Clinically significant vitamin B12 deficiency Severe systemic medical illness (eg end-stage cardiac disease, …)