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Subclinical epileptiform activity in the Alzheimer continuum: association with disease, cognition and detection method.
Nous, Amber; Seynaeve, Laura; Feys, Odile; Wens, Vincent; De Tiège, Xavier; Van Mierlo, Pieter; Baroumand, Amir G; Nieboer, Koenraad; Allemeersch, Gert-Jan; Mangelschots, Shana; Michiels, Veronique; van der Zee, Julie; Van Broeckhoven, Christine; Ribbens, Annemie; Houbrechts, Ruben; De Witte, Sara; Wittens, Mandy Melissa Jane; Bjerke, Maria; Vanlersberghe, Caroline; Ceyssens, Sarah; Nagels, Guy; Smolders, Ilse; Engelborghs, Sebastiaan.
Afiliación
  • Nous A; Department of Neurology, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
  • Seynaeve L; Neuroprotection and Neuromodulation (NEUR) Research Group, Center for Neurosciences, Vrije Universiteit Brussel, Laarbeeklaan 103, Brussels, Belgium.
  • Feys O; Department of Biomedical Sciences, Universiteit Antwerpen, Antwerp, Belgium.
  • Wens V; Laboratory of Pharmaceutical Chemistry, Drug Analysis and Drug Information (FASC), Research Group Experimental Pharmacology (EFAR), Center for Neurosciences, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
  • De Tiège X; Department of Neurology, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
  • Van Mierlo P; Neuroprotection and Neuromodulation (NEUR) Research Group, Center for Neurosciences, Vrije Universiteit Brussel, Laarbeeklaan 103, Brussels, Belgium.
  • Baroumand AG; Department of Neurology, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), Hôpital Erasme, Brussels, Belgium.
  • Nieboer K; Laboratoire de Neuroimagerie Et Neuroanatomie Translationnelles (LN2T), Université Libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Brussels, Belgium.
  • Allemeersch GJ; Laboratoire de Neuroimagerie Et Neuroanatomie Translationnelles (LN2T), Université Libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Brussels, Belgium.
  • Mangelschots S; Department of Translational Neuroimaging, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), Hôpital Erasme, Brussels, Belgium.
  • Michiels V; Laboratoire de Neuroimagerie Et Neuroanatomie Translationnelles (LN2T), Université Libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Brussels, Belgium.
  • van der Zee J; Department of Translational Neuroimaging, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), Hôpital Erasme, Brussels, Belgium.
  • Van Broeckhoven C; Epilog NV, Ghent, Belgium.
  • Ribbens A; Epilog NV, Ghent, Belgium.
  • Houbrechts R; Department of Radiology, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, Belgium.
  • De Witte S; Department of Radiology, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, Belgium.
  • Wittens MMJ; Neuroprotection and Neuromodulation (NEUR) Research Group, Center for Neurosciences, Vrije Universiteit Brussel, Laarbeeklaan 103, Brussels, Belgium.
  • Bjerke M; Department of Biomedical Sciences, Universiteit Antwerpen, Antwerp, Belgium.
  • Vanlersberghe C; Department of Neurology, Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
  • Ceyssens S; Department of Biomedical Sciences, Universiteit Antwerpen, Antwerp, Belgium.
  • Nagels G; Neurodegenerative Brain Diseases, VIB Center for Molecular Neurology, Antwerp, Belgium.
  • Smolders I; Department of Biomedical Sciences, Universiteit Antwerpen, Antwerp, Belgium.
  • Engelborghs S; Neurodegenerative Brain Diseases, VIB Center for Molecular Neurology, Antwerp, Belgium.
Alzheimers Res Ther ; 16(1): 19, 2024 01 23.
Article en En | MEDLINE | ID: mdl-38263073
ABSTRACT

BACKGROUND:

Epileptic seizures are an established comorbidity of Alzheimer's disease (AD). Subclinical epileptiform activity (SEA) as detected by 24-h electroencephalography (EEG) or magneto-encephalography (MEG) has been reported in temporal regions of clinically diagnosed AD patients. Although epileptic activity in AD probably arises in the mesial temporal lobe, electrical activity within this region might not propagate to EEG scalp electrodes and could remain undetected by standard EEG. However, SEA might lead to faster cognitive decline in AD.

AIMS:

1. To estimate the prevalence of SEA and interictal epileptic discharges (IEDs) in a well-defined cohort of participants belonging to the AD continuum, including preclinical AD subjects, as compared with cognitively healthy controls. 2. To evaluate whether long-term-EEG (LTM-EEG), high-density-EEG (hd-EEG) or MEG is superior to detect SEA in AD. 3. To characterise AD patients with SEA based on clinical, neuropsychological and neuroimaging parameters.

METHODS:

Subjects (n = 49) belonging to the AD continuum were diagnosed according to the 2011 NIA-AA research criteria, with a high likelihood of underlying AD pathophysiology. Healthy volunteers (n = 24) scored normal on neuropsychological testing and were amyloid negative. None of the participants experienced a seizure before. Subjects underwent LTM-EEG and/or 50-min MEG and/or 50-min hd-EEG to detect IEDs.

RESULTS:

We found an increased prevalence of SEA in AD subjects (31%) as compared to controls (8%) (p = 0.041; Fisher's exact test), with increasing prevalence over the disease course (50% in dementia, 27% in MCI and 25% in preclinical AD). Although MEG (25%) did not withhold a higher prevalence of SEA in AD as compared to LTM-EEG (19%) and hd-EEG (19%), MEG was significantly superior to detect spikes per 50 min (p = 0.002; Kruskall-Wallis test). AD patients with SEA scored worse on the RBANS visuospatial and attention subset (p = 0.009 and p = 0.05, respectively; Mann-Whitney U test) and had higher left frontal, (left) temporal and (left and right) entorhinal cortex volumes than those without.

CONCLUSION:

We confirmed that SEA is increased in the AD continuum as compared to controls, with increasing prevalence with AD disease stage. In AD patients, SEA is associated with more severe visuospatial and attention deficits and with increased left frontal, (left) temporal and entorhinal cortex volumes. TRIAL REGISTRATION Clinicaltrials.gov, NCT04131491. 12/02/2020.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer / Disfunción Cognitiva Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Alzheimers Res Ther Año: 2024 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer / Disfunción Cognitiva Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Alzheimers Res Ther Año: 2024 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Reino Unido