Alzheimer's Disease with Epileptiform EEG Activity: Abnormal Cortical Sources of Resting State Delta Rhythms in Patients with Amnesic Mild Cognitive Impairment
Patients with amnesic mild cognitive impairment due to Alzheimer's disease (ADMCI) typically show a "slowing" of cortical resting-state eyes-closed electroencephalographic (rsEEG) rhythms. Some of them also show subclinical, non-convulsive, and epileptiform EEG activity (EEA) with an...
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| Published in: | Journal of Alzheimer's disease Vol. 88; no. 3; p. 903 |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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01.01.2022
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| ISSN: | 1875-8908, 1875-8908 |
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| Abstract | Patients with amnesic mild cognitive impairment due to Alzheimer's disease (ADMCI) typically show a "slowing" of cortical resting-state eyes-closed electroencephalographic (rsEEG) rhythms. Some of them also show subclinical, non-convulsive, and epileptiform EEG activity (EEA) with an unclear relationship with that "slowing."
Here we tested the hypothesis that the "slowing" of rsEEG rhythms is related to EEA in ADMCI patients.
Clinical and instrumental datasets in 62 ADMCI patients and 38 normal elderly (Nold) subjects were available in a national archive. No participant had received a clinical diagnosis of epilepsy. The eLORETA freeware estimated rsEEG cortical sources. The area under the receiver operating characteristic curve (AUROCC) indexed the accuracy of eLORETA solutions in the classification between ADMCI-EEA and ADMCI-noEEA individuals.
EEA was observed in 15% (N = 8) of the ADMCI patients. The ADMCI-EEA group showed: 1) more abnormal Aβ 42 levels in the cerebrospinal fluid as compared to the ADMCI-noEEA group and 2) higher temporal and occipital delta (<4 Hz) rsEEG source activities as compared to the ADMCI-noEEA and Nold groups. Those source activities showed moderate accuracy (AUROCC = 0.70-0.75) in the discrimination between ADMCI-noEEA versus ADMCI-EEA individuals.
It can be speculated that in ADMCI-EEA patients, AD-related amyloid neuropathology may be related to an over-excitation in neurophysiological low-frequency (delta) oscillatory mechanisms underpinning cortical arousal and quiet vigilance. |
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| AbstractList | Patients with amnesic mild cognitive impairment due to Alzheimer's disease (ADMCI) typically show a "slowing" of cortical resting-state eyes-closed electroencephalographic (rsEEG) rhythms. Some of them also show subclinical, non-convulsive, and epileptiform EEG activity (EEA) with an unclear relationship with that "slowing."
Here we tested the hypothesis that the "slowing" of rsEEG rhythms is related to EEA in ADMCI patients.
Clinical and instrumental datasets in 62 ADMCI patients and 38 normal elderly (Nold) subjects were available in a national archive. No participant had received a clinical diagnosis of epilepsy. The eLORETA freeware estimated rsEEG cortical sources. The area under the receiver operating characteristic curve (AUROCC) indexed the accuracy of eLORETA solutions in the classification between ADMCI-EEA and ADMCI-noEEA individuals.
EEA was observed in 15% (N = 8) of the ADMCI patients. The ADMCI-EEA group showed: 1) more abnormal Aβ 42 levels in the cerebrospinal fluid as compared to the ADMCI-noEEA group and 2) higher temporal and occipital delta (<4 Hz) rsEEG source activities as compared to the ADMCI-noEEA and Nold groups. Those source activities showed moderate accuracy (AUROCC = 0.70-0.75) in the discrimination between ADMCI-noEEA versus ADMCI-EEA individuals.
It can be speculated that in ADMCI-EEA patients, AD-related amyloid neuropathology may be related to an over-excitation in neurophysiological low-frequency (delta) oscillatory mechanisms underpinning cortical arousal and quiet vigilance. Patients with amnesic mild cognitive impairment due to Alzheimer's disease (ADMCI) typically show a "slowing" of cortical resting-state eyes-closed electroencephalographic (rsEEG) rhythms. Some of them also show subclinical, non-convulsive, and epileptiform EEG activity (EEA) with an unclear relationship with that "slowing."BACKGROUNDPatients with amnesic mild cognitive impairment due to Alzheimer's disease (ADMCI) typically show a "slowing" of cortical resting-state eyes-closed electroencephalographic (rsEEG) rhythms. Some of them also show subclinical, non-convulsive, and epileptiform EEG activity (EEA) with an unclear relationship with that "slowing."Here we tested the hypothesis that the "slowing" of rsEEG rhythms is related to EEA in ADMCI patients.OBJECTIVEHere we tested the hypothesis that the "slowing" of rsEEG rhythms is related to EEA in ADMCI patients.Clinical and instrumental datasets in 62 ADMCI patients and 38 normal elderly (Nold) subjects were available in a national archive. No participant had received a clinical diagnosis of epilepsy. The eLORETA freeware estimated rsEEG cortical sources. The area under the receiver operating characteristic curve (AUROCC) indexed the accuracy of eLORETA solutions in the classification between ADMCI-EEA and ADMCI-noEEA individuals.METHODSClinical and instrumental datasets in 62 ADMCI patients and 38 normal elderly (Nold) subjects were available in a national archive. No participant had received a clinical diagnosis of epilepsy. The eLORETA freeware estimated rsEEG cortical sources. The area under the receiver operating characteristic curve (AUROCC) indexed the accuracy of eLORETA solutions in the classification between ADMCI-EEA and ADMCI-noEEA individuals.EEA was observed in 15% (N = 8) of the ADMCI patients. The ADMCI-EEA group showed: 1) more abnormal Aβ42 levels in the cerebrospinal fluid as compared to the ADMCI-noEEA group and 2) higher temporal and occipital delta (<4 Hz) rsEEG source activities as compared to the ADMCI-noEEA and Nold groups. Those source activities showed moderate accuracy (AUROCC = 0.70-0.75) in the discrimination between ADMCI-noEEA versus ADMCI-EEA individuals.RESULTSEEA was observed in 15% (N = 8) of the ADMCI patients. The ADMCI-EEA group showed: 1) more abnormal Aβ42 levels in the cerebrospinal fluid as compared to the ADMCI-noEEA group and 2) higher temporal and occipital delta (<4 Hz) rsEEG source activities as compared to the ADMCI-noEEA and Nold groups. Those source activities showed moderate accuracy (AUROCC = 0.70-0.75) in the discrimination between ADMCI-noEEA versus ADMCI-EEA individuals.It can be speculated that in ADMCI-EEA patients, AD-related amyloid neuropathology may be related to an over-excitation in neurophysiological low-frequency (delta) oscillatory mechanisms underpinning cortical arousal and quiet vigilance.CONCLUSIONIt can be speculated that in ADMCI-EEA patients, AD-related amyloid neuropathology may be related to an over-excitation in neurophysiological low-frequency (delta) oscillatory mechanisms underpinning cortical arousal and quiet vigilance. |
| Author | Marizzoni, Moira Lizio, Roberta Cifelli, Pierangelo Di Bonaventura, Carlo Stocchi, Fabrizio Di Gennaro, Giancarlo Del Percio, Claudio Salamone, Enrico M Arnaldi, Dario Babiloni, Claudio Ferri, Raffaele Eldellaa, Ali Palma, Eleonora Soricelli, Andrea Famà, Francesco Bruno, Giuseppe Nobili, Flavio Tucci, Federico Noce, Giuseppe Frisoni, Giovanni B |
| Author_xml | – sequence: 1 givenname: Claudio surname: Babiloni fullname: Babiloni, Claudio organization: Hospital San Raffaele Cassino, Cassino (FR), Italy – sequence: 2 givenname: Giuseppe surname: Noce fullname: Noce, Giuseppe organization: IRCCS Synlab SDN, Naples, Italy – sequence: 3 givenname: Carlo surname: Di Bonaventura fullname: Di Bonaventura, Carlo organization: Epilepsy Unit, Department of Neurosciences/Mental Health, Sapienza University of Rome, Rome, Italy – sequence: 4 givenname: Roberta surname: Lizio fullname: Lizio, Roberta organization: IRCCS Synlab SDN, Naples, Italy – sequence: 5 givenname: Ali surname: Eldellaa fullname: Eldellaa, Ali organization: Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, Rome, Italy – sequence: 6 givenname: Federico surname: Tucci fullname: Tucci, Federico organization: Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, Rome, Italy – sequence: 7 givenname: Enrico M surname: Salamone fullname: Salamone, Enrico M organization: Epilepsy Unit, Department of Neurosciences/Mental Health, Sapienza University of Rome, Rome, Italy – sequence: 8 givenname: Raffaele surname: Ferri fullname: Ferri, Raffaele organization: Oasi Research Institute - IRCCS, Troina, Italy – sequence: 9 givenname: Andrea surname: Soricelli fullname: Soricelli, Andrea organization: Department of Motor Sciences and Healthiness, University of Naples Parthenope, Naples, Italy – sequence: 10 givenname: Flavio surname: Nobili fullname: Nobili, Flavio organization: Department of Neuroscience (DiNOGMI), University of Genoa, Genoa, Italy – sequence: 11 givenname: Francesco surname: Famà fullname: Famà, Francesco organization: Clinical Neurology, IRCCS Hospital Policlinico San Martino, Genoa, Italy – sequence: 12 givenname: Dario surname: Arnaldi fullname: Arnaldi, Dario organization: Clinical Neurology, IRCCS Hospital Policlinico San Martino, Genoa, Italy – sequence: 13 givenname: Eleonora surname: Palma fullname: Palma, Eleonora organization: Pasteur Institute-Cenci Bolognetti Foundation, Rome, Italy – sequence: 14 givenname: Pierangelo surname: Cifelli fullname: Cifelli, Pierangelo organization: Department of Applied and Biotechnological Clinical Sciences, University of L'Aquila, L'Aquila, Italy – sequence: 15 givenname: Moira surname: Marizzoni fullname: Marizzoni, Moira organization: Laboratory of Alzheimer's Neuroimaging and Epidemiology, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy – sequence: 16 givenname: Fabrizio surname: Stocchi fullname: Stocchi, Fabrizio organization: IRCCS San Raffaele Roma, Rome, Italy – sequence: 17 givenname: Giuseppe surname: Bruno fullname: Bruno, Giuseppe organization: Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy – sequence: 18 givenname: Giancarlo surname: Di Gennaro fullname: Di Gennaro, Giancarlo organization: IRCCS Neuromed, Pozzilli, (IS), Italy – sequence: 19 givenname: Giovanni B surname: Frisoni fullname: Frisoni, Giovanni B organization: Memory Clinic and LANVIE - Laboratory of Neuroimaging of Aging, University Hospitals and University of Geneva, Geneva, Switzerland – sequence: 20 givenname: Claudio surname: Del Percio fullname: Del Percio, Claudio organization: Department of Physiology and Pharmacology "Vittorio Erspamer", Sapienza University of Rome, Rome, Italy |
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| Keywords | Epileptiform EEG activity resting state electroencephalographic rhythms exact low-resolution brain electromagnetic source tomography mild cognitive impairment due to Alzheimer’s disease |
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| Title | Alzheimer's Disease with Epileptiform EEG Activity: Abnormal Cortical Sources of Resting State Delta Rhythms in Patients with Amnesic Mild Cognitive Impairment |
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