scholarly journals EEG spectral power in phasic and tonic REM sleep: different patterns in young adults and children

2016 ◽  
Vol 25 (3) ◽  
pp. 269-277 ◽  
Author(s):  
Péter Simor ◽  
Ferenc Gombos ◽  
Sára Szakadát ◽  
Piroska Sándor ◽  
Róbert Bódizs
2021 ◽  
Vol 12 ◽  
Author(s):  
Katia Gagnon ◽  
Christianne Bolduc ◽  
Laurianne Bastien ◽  
Roger Godbout

We tested the hypothesis of an atypical scalp distribution of electroencephalography (EEG) activity during Rapid Eye Movement (REM) sleep in young autistic adults. EEG spectral activity and ratios along the anteroposterior axis and across hemispheres were compared in 16 neurotypical (NT) young adults and 17 individuals with autism spectrum disorder (ASD). EEG spectral power was lower in the ASD group over the bilateral central and right parietal (beta activity) as well as bilateral occipital (beta, theta, and total activity) recording sites. The NT group displayed a significant posterior polarity of intra-hemispheric EEG activity while EEG activity was more evenly or anteriorly distributed in ASD participants. No significant inter-hemispheric EEG lateralization was found. Correlations between EEG distribution and ASD symptoms using the Autism Diagnostic Interview-Revised (ADI-R) showed that a higher posterior ratio was associated with a better ADI-R score on communication skills, whereas a higher anterior ratio was related to more restricted interests and repetitive behaviors. EEG activity thus appears to be atypically distributed over the scalp surface in young adults with autism during REM sleep within cerebral hemispheres, and this correlates with some ASD symptoms. These suggests the existence in autism of a common substrate between some of the symptoms of ASD and an atypical organization and/or functioning of the thalamo-cortical loop during REM sleep.


2014 ◽  
Vol 28 (4) ◽  
pp. 580-590 ◽  
Author(s):  
Glenn L. Kitsune ◽  
Celeste H. M. Cheung ◽  
Daniel Brandeis ◽  
Tobias Banaschewski ◽  
Philip Asherson ◽  
...  

1993 ◽  
Vol 2 (1) ◽  
pp. 21-27 ◽  
Author(s):  
D. WATERMAN ◽  
M. ELTON ◽  
W. HOFMAN ◽  
J. C. WOESTENBURG ◽  
A. KOK

2021 ◽  
Vol 17 (S6) ◽  
Author(s):  
Claire André ◽  
Marie‐Ève Martineau‐Dussault ◽  
Véronique Daneault ◽  
Hélène Blais ◽  
Dominique Lorrain ◽  
...  

2020 ◽  
Vol 16 (S4) ◽  
Author(s):  
Claire Andre ◽  
Stéphane Rehel ◽  
Elizabeth Kuhn ◽  
Edelweiss Touron ◽  
Florence Mézenge ◽  
...  

2021 ◽  
Vol 11 (3) ◽  
pp. 330
Author(s):  
Dalton J. Edwards ◽  
Logan T. Trujillo

Traditionally, quantitative electroencephalography (QEEG) studies collect data within controlled laboratory environments that limit the external validity of scientific conclusions. To probe these validity limits, we used a mobile EEG system to record electrophysiological signals from human participants while they were located within a controlled laboratory environment and an uncontrolled outdoor environment exhibiting several moderate background influences. Participants performed two tasks during these recordings, one engaging brain activity related to several complex cognitive functions (number sense, attention, memory, executive function) and the other engaging two default brain states. We computed EEG spectral power over three frequency bands (theta: 4–7 Hz, alpha: 8–13 Hz, low beta: 14–20 Hz) where EEG oscillatory activity is known to correlate with the neurocognitive states engaged by these tasks. Null hypothesis significance testing yielded significant EEG power effects typical of the neurocognitive states engaged by each task, but only a beta-band power difference between the two background recording environments during the default brain state. Bayesian analysis showed that the remaining environment null effects were unlikely to reflect measurement insensitivities. This overall pattern of results supports the external validity of laboratory EEG power findings for complex and default neurocognitive states engaged within moderately uncontrolled environments.


2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Katherine R. Dobbs ◽  
Paula Embury ◽  
Emmily Koech ◽  
Sidney Ogolla ◽  
Stephen Munga ◽  
...  

Abstract Background Age-related changes in adaptive and innate immune cells have been associated with a decline in effective immunity and chronic, low-grade inflammation. Epigenetic, transcriptional, and functional changes in monocytes occur with aging, though most studies to date have focused on differences between young adults and the elderly in populations with European ancestry; few data exist regarding changes that occur in circulating monocytes during the first few decades of life or in African populations. We analyzed DNA methylation profiles, cytokine production, and inflammatory gene expression profiles in monocytes from young adults and children from western Kenya. Results We identified several hypo- and hyper-methylated CpG sites in monocytes from Kenyan young adults vs. children that replicated findings in the current literature of differential DNA methylation in monocytes from elderly persons vs. young adults across diverse populations. Differentially methylated CpG sites were also noted in gene regions important to inflammation and innate immune responses. Monocytes from Kenyan young adults vs. children displayed increased production of IL-8, IL-10, and IL-12p70 in response to TLR4 and TLR2/1 stimulation as well as distinct inflammatory gene expression profiles. Conclusions These findings complement previous reports of age-related methylation changes in isolated monocytes and provide novel insights into the role of age-associated changes in innate immune functions.


2013 ◽  
Vol 47 (5) ◽  
pp. e1.20-e1
Author(s):  
Nour Boutros ◽  
Mary Catherine Norcia ◽  
Jamila Sammouda ◽  
Chi-Lan Tran ◽  
Isabelle Pearson ◽  
...  

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