Separability of Different Negative Components of the Event-Related Potential Associated with Auditory Stimulus Processing

1986 ◽  
Vol 23 (6) ◽  
pp. 613-623 ◽  
Author(s):  
K. Alho ◽  
P. Paavilainen ◽  
K. Reinikainen ◽  
M. Sams ◽  
R. Näätänen
Author(s):  
A. B. Rebreikina ◽  
D. F. Kleeva ◽  
G. A. Soghoyan ◽  
O. V. Sysoeva

NeuroImage ◽  
2002 ◽  
Vol 17 (1) ◽  
pp. 110-127 ◽  
Author(s):  
Jürgen Gallinat ◽  
Christoph Mulert ◽  
Malek Bajbouj ◽  
Werner M. Herrmann ◽  
Jürgen Schunter ◽  
...  

2022 ◽  
Vol 13 ◽  
Author(s):  
Chiara F. Tagliabue ◽  
Greta Varesio ◽  
Veronica Mazza

Electroencephalography (EEG) studies investigating visuo-spatial working memory (vWM) in aging typically adopt an event-related potential (ERP) analysis approach that has shed light on the age-related changes during item retention and retrieval. However, this approach does not fully enable a detailed description of the time course of the neural dynamics related to aging. The most frequent age-related changes in brain activity have been described by two influential models of neurocognitive aging, the Hemispheric Asymmetry Reduction in Older Adults (HAROLD) and the Posterior-Anterior Shift in Aging (PASA). These models posit that older adults tend to recruit additional brain areas (bilateral as predicted by HAROLD and anterior as predicted by PASA) when performing several cognitive tasks. We tested younger (N = 36) and older adults (N = 35) in a typical vWM task (delayed match-to-sample) where participants have to retain items and then compare them to a sample. Through a data-driven whole scalp EEG analysis we aimed at characterizing the temporal dynamics of the age-related activations predicted by the two models, both across and within different stages of stimulus processing. Behaviorally, younger outperformed older adults. The EEG analysis showed that older adults engaged supplementary bilateral posterior and frontal sites when processing different levels of memory load, in line with both HAROLD and PASA-like activations. Interestingly, these age-related supplementary activations dynamically developed over time. Indeed, they varied across different stages of stimulus processing, with HAROLD-like modulations being mainly present during item retention, and PASA-like activity during both retention and retrieval. Overall, the present results suggest that age-related neural changes are not a phenomenon indiscriminately present throughout all levels of cognitive processing.


2021 ◽  
Vol 13 ◽  
Author(s):  
Farooq Kamal ◽  
Cassandra Morrison ◽  
Kenneth Campbell ◽  
Vanessa Taler

Much research effort is currently devoted to the development of a simple, low-cost method to determine early signs of Alzheimer’s disease (AD) pathology. The present study employs a simple paradigm in which event-related potentials (ERPs) were recorded to a single auditory stimulus that was presented rapidly or very slowly while the participant was engaged in a visual task. A multi-channel EEG was recorded in 20 healthy older adults and 20 people with mild cognitive impairment (MCI). In two different conditions, a single 80 dB sound pressure level (SPL) auditory stimulus was presented every 1.5 s (fast condition) or every 12.0 s (slow condition). Participants were instructed to watch a silent video and ignore the auditory stimuli. Auditory processing thus occurred passively. When the auditory stimuli were presented rapidly (every 1.5 s), N1 and P2 amplitudes did not differ between the two groups. When the stimuli were presented very slowly, the amplitude of N1 and P2 increased in both groups and their latencies were prolonged. The amplitude of N1 did not significantly differ between the two groups. However, the subsequent positivity was reduced in people with MCI compared to healthy older adults. This late positivity in the slow condition may reflect a delayed P2 or a summation of a composite P2 + P3a. In people with MCI, the priority of processing may not be switched from the visual task to the potentially much more relevant auditory input. ERPs offer promise as a means to identify the pathology underlying cognitive impairment associated with MCI.


1994 ◽  
Vol 49 (4) ◽  
pp. M183-M188 ◽  
Author(s):  
C. Dodt ◽  
R. Pietrowsky ◽  
A. Sewing ◽  
A. Zabel ◽  
H. L. Fehm ◽  
...  

1990 ◽  
Vol 27 (6) ◽  
pp. 627-640 ◽  
Author(s):  
Marie-Hélène Giard ◽  
François Perrin ◽  
Jacques Pernier ◽  
Patrick Bouchet

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