[article]
Titre : |
Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis |
Type de document : |
Texte imprimé et/ou numérique |
Auteurs : |
M. S. SIDOROV, Auteur ; G. M. DECK, Auteur ; M. DOLATSHAHI, Auteur ; R. L. THIBERT, Auteur ; L. M. BIRD, Auteur ; C. J. CHU, Auteur ; B. D. PHILPOT, Auteur |
Article en page(s) : |
p.17 |
Langues : |
Anglais (eng) |
Mots-clés : |
Angelman syndrome Biomarker Delta Eeg Mouse model Outcome measure Ube3a |
Index. décimale : |
PER Périodiques |
Résumé : |
BACKGROUND: Clinicians have qualitatively described rhythmic delta activity as a prominent EEG abnormality in individuals with Angelman syndrome, but this phenotype has yet to be rigorously quantified in the clinical population or validated in a preclinical model. Here, we sought to quantitatively measure delta rhythmicity and evaluate its fidelity as a biomarker. METHODS: We quantified delta oscillations in mouse and human using parallel spectral analysis methods and measured regional, state-specific, and developmental changes in delta rhythms in a patient population. RESULTS: Delta power was broadly increased and more dynamic in both the Angelman syndrome mouse model, relative to wild-type littermates, and in children with Angelman syndrome, relative to age-matched neurotypical controls. Enhanced delta oscillations in children with Angelman syndrome were present during wakefulness and sleep, were generalized across the neocortex, and were more pronounced at earlier ages. CONCLUSIONS: Delta rhythmicity phenotypes can serve as reliable biomarkers for Angelman syndrome in both preclinical and clinical settings. |
En ligne : |
http://dx.doi.org/10.1186/s11689-017-9195-8 |
Permalink : |
https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=350 |
in Journal of Neurodevelopmental Disorders > 9-1 (December 2017) . - p.17
[article] Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis [Texte imprimé et/ou numérique] / M. S. SIDOROV, Auteur ; G. M. DECK, Auteur ; M. DOLATSHAHI, Auteur ; R. L. THIBERT, Auteur ; L. M. BIRD, Auteur ; C. J. CHU, Auteur ; B. D. PHILPOT, Auteur . - p.17. Langues : Anglais ( eng) in Journal of Neurodevelopmental Disorders > 9-1 (December 2017) . - p.17
Mots-clés : |
Angelman syndrome Biomarker Delta Eeg Mouse model Outcome measure Ube3a |
Index. décimale : |
PER Périodiques |
Résumé : |
BACKGROUND: Clinicians have qualitatively described rhythmic delta activity as a prominent EEG abnormality in individuals with Angelman syndrome, but this phenotype has yet to be rigorously quantified in the clinical population or validated in a preclinical model. Here, we sought to quantitatively measure delta rhythmicity and evaluate its fidelity as a biomarker. METHODS: We quantified delta oscillations in mouse and human using parallel spectral analysis methods and measured regional, state-specific, and developmental changes in delta rhythms in a patient population. RESULTS: Delta power was broadly increased and more dynamic in both the Angelman syndrome mouse model, relative to wild-type littermates, and in children with Angelman syndrome, relative to age-matched neurotypical controls. Enhanced delta oscillations in children with Angelman syndrome were present during wakefulness and sleep, were generalized across the neocortex, and were more pronounced at earlier ages. CONCLUSIONS: Delta rhythmicity phenotypes can serve as reliable biomarkers for Angelman syndrome in both preclinical and clinical settings. |
En ligne : |
http://dx.doi.org/10.1186/s11689-017-9195-8 |
Permalink : |
https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=350 |
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