TY - JOUR
T1 - Resting state cortical electroencephalographic rhythms are related to gray matter volume in subjects with mild cognitive impairment and Alzheimer's disease
AU - Babiloni, Claudio
AU - Carducci, Filippo
AU - Lizio, Roberta
AU - Vecchio, Fabrizio
AU - Baglieri, Annalisa
AU - Bernardini, Silvia
AU - Cavedo, Enrica
AU - Bozzao, Alessandro
AU - Buttinelli, Carla
AU - Esposito, Fabrizio
AU - Giubilei, Franco
AU - Guizzaro, Antonio
AU - Marino, Silvia
AU - Montella, Patrizia
AU - Quattrocchi, Carlo C.
AU - Redolfi, Alberto
AU - Soricelli, Andrea
AU - Tedeschi, Gioacchino
AU - Ferri, Raffaele
AU - Rossi-Fedele, Giancarlo
AU - Ursini, Francesca
AU - Scrascia, Federica
AU - Vernieri, Fabrizio
AU - Pedersen, Torleif Jan
AU - Hardemark, Hans-Goran
AU - Rossini, Paolo Maria
AU - Frisoni, Giovanni B.
PY - 2013
Y1 - 2013
N2 - Cortical gray matter volume and resting state cortical electroencephalographic rhythms are typically abnormal in subjects with amnesic mild cognitive impairment (MCI) and Alzheimer's disease (AD). Here we tested the hypothesis that in amnesic MCI and AD subjects, abnormalities of EEG rhythms are a functional reflection of cortical atrophy across the disease. Eyes-closed resting state EEG data were recorded in 57 healthy elderly (Nold), 102 amnesic MCI, and 108 AD patients. Cortical gray matter volume was indexed by magnetic resonance imaging recorded in the MCI and AD subjects according to Alzheimer's disease neuroimaging initiative project (http://www.adni-info.org/). EEG rhythms of interest were delta (2-4 Hz), theta (4-8 Hz), alpha1 (8-10.5 Hz), alpha2 (10.5-13 Hz), beta1 (13-20 Hz), beta2 (20-30 Hz), and gamma (30-40 Hz). These rhythms were indexed by LORETA. Compared with the Nold, the MCI showed a decrease in amplitude of alpha 1 sources. With respect to the Nold and MCI, the AD showed an amplitude increase of delta sources, along with a strong amplitude reduction of alpha 1 sources. In the MCI and AD subjects as a whole group, the lower the cortical gray matter volume, the higher the delta sources, the lower the alpha 1 sources. The better the score to cognitive tests the higher the gray matter volume, the lower the pathological delta sources, and the higher the alpha sources. These results suggest that in amnesic MCI and AD subjects, abnormalities of resting state cortical EEG rhythms are not epiphenomena but are strictly related to neurodegeneration (atrophy of cortical gray matter) and cognition.
AB - Cortical gray matter volume and resting state cortical electroencephalographic rhythms are typically abnormal in subjects with amnesic mild cognitive impairment (MCI) and Alzheimer's disease (AD). Here we tested the hypothesis that in amnesic MCI and AD subjects, abnormalities of EEG rhythms are a functional reflection of cortical atrophy across the disease. Eyes-closed resting state EEG data were recorded in 57 healthy elderly (Nold), 102 amnesic MCI, and 108 AD patients. Cortical gray matter volume was indexed by magnetic resonance imaging recorded in the MCI and AD subjects according to Alzheimer's disease neuroimaging initiative project (http://www.adni-info.org/). EEG rhythms of interest were delta (2-4 Hz), theta (4-8 Hz), alpha1 (8-10.5 Hz), alpha2 (10.5-13 Hz), beta1 (13-20 Hz), beta2 (20-30 Hz), and gamma (30-40 Hz). These rhythms were indexed by LORETA. Compared with the Nold, the MCI showed a decrease in amplitude of alpha 1 sources. With respect to the Nold and MCI, the AD showed an amplitude increase of delta sources, along with a strong amplitude reduction of alpha 1 sources. In the MCI and AD subjects as a whole group, the lower the cortical gray matter volume, the higher the delta sources, the lower the alpha 1 sources. The better the score to cognitive tests the higher the gray matter volume, the lower the pathological delta sources, and the higher the alpha sources. These results suggest that in amnesic MCI and AD subjects, abnormalities of resting state cortical EEG rhythms are not epiphenomena but are strictly related to neurodegeneration (atrophy of cortical gray matter) and cognition.
KW - Aged
KW - Alzheimer Disease
KW - Atrophy
KW - Brain
KW - Electroencephalography
KW - Female
KW - Humans
KW - Magnetic Resonance Imaging
KW - Male
KW - Mild Cognitive Impairment
KW - Nerve Degeneration
KW - Rest
KW - Aged
KW - Alzheimer Disease
KW - Atrophy
KW - Brain
KW - Electroencephalography
KW - Female
KW - Humans
KW - Magnetic Resonance Imaging
KW - Male
KW - Mild Cognitive Impairment
KW - Nerve Degeneration
KW - Rest
UR - http://hdl.handle.net/10807/54068
U2 - 10.1002/hbm.22005
DO - 10.1002/hbm.22005
M3 - Article
SN - 1097-0193
VL - 34
SP - 1427
EP - 1446
JO - Human Brain Mapping
JF - Human Brain Mapping
ER -