Reduced Resting-State EEG Power Spectra and Functional Connectivity after 24 and 36 Hours of Sleep Deprivation

Lian, Jie; Xu, Lin; Song, Tao; Peng, Ziyi; Zhang, Zheyuan; Xu, An; Chen, Shu-Fang; Zhong, Xiao; Shao, Yuanyuan

doi:10.3390/brainsci13060949

Cited by 6 publications

(4 citation statements)

References 88 publications

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“…Previous studies have shown the dose effects of sleep deprivation. As the duration of sleep deprivation is prolonged, cognitive impairment becomes more severe (Doherty et al, 2005;Drummond et al, 2000;Lian et al, 2023;Patel et al, 2008;Shao et al, 2014;Shao et al, 2013). We identified that attention impairment caused by ATSD occurred to varying degrees across the occipital (right inferior occipital gyrus), parietal (bilateral superior parietal lobule), and frontal lobes (left middle frontal gyrus and right inferior frontal gyrus), which is consistent with previous research.…”

Section: Discussionsupporting

confidence: 90%

Effect of 24-h and 36-h Acute Total Sleep Deprivation on Human Attention: An Activation Likelihood Estimation Meta-analysis

Chen,

Song,

Peng

et al. 2023

Preprint

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Background: Currently, there is no consensus on the effect of 24-h and 36-h acute total sleep deprivation (ATSD) on human attention. This activation likelihood estimation (ALE) meta-analysis aimed to compare the different patterns of functional magnetic resonance imaging (fMRI activation) between 24-h and 36-h ATSD across attention tasks. Methods: We used GingerALE 2.3.6 software to conduct coordinate-based ALE meta-analysis. The literature related to sleep deprivation, attention, and neuroimaging was searched in four databases: CNKI, PubMed, Web of Science, and PsycINFO from November 1980 to March 2023. Results: We included 16 fMRI-related articles, with 383 participants and 95 foci. The findings revealed that 24-h ATSD and 36-h ATSD may impair different brain areas. After 24-h ATSD, there was significantly reduced brain activation in the parietal-occipital attention lobes and the salience network, including the bilateral superior parietal lobule, right inferior occipital gyrus, and left insula. Increased activation was observed in the sub-lobar regions, including the bilateral thalamus. After 36-h ATSD, there was significantly reduced activation in the frontoparietal attention network, including the left middle frontal gyrus and the right inferior frontal gyrus. Conclusions: This ALE meta-analysis revealed that prolonged ATSD leads to more severe temporary brain damage and a cumulative decrease in the external stimuli captured by humans. This primarily affects the frontal-parietal-occipital attention network and the salience network. Thalamic activation may compensate for dysfunction in the parietal-occipital attention network after 24-h ATSD. Sleep deprivation duration plays a crucial role in the extent of attention impairment.

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Section: Discussionsupporting

confidence: 90%

Effect of 24-h and 36-h Acute Total Sleep Deprivation on Human Attention: An Activation Likelihood Estimation Meta-analysis

Chen,

Song,

Peng

et al. 2023

Preprint

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“…Wang C. et al, using surface morphological analysis and graph theoretical analysis, showed that sleep restriction decreases cortical thickness and enhances the topological properties of the structural covariance network [43]. Additionally, total sleep deprivation affects functional connectivity, as observed by EEG recordings [48] and event-related potential analysis [49]. However, the impairment induced by sleep deprivation appears to be temporary and reversible with sufficient sleep, as demonstrated by resting-state functional MRI data [50].…”

Section: Discussionmentioning

confidence: 99%

The Effect of Sleep Deprivation on Brain Fingerprint Stability: A Magnetoencephalography Validation Study

Ambrosanio,

Troisi Lopez,

Polverino

et al. 2024

Sensors

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This study examined the stability of the functional connectome (FC) over time using fingerprint analysis in healthy subjects. Additionally, it investigated how a specific stressor, namely sleep deprivation, affects individuals’ differentiation. To this aim, 23 healthy young adults underwent magnetoencephalography (MEG) recording at three equally spaced time points within 24 h: 9 a.m., 9 p.m., and 9 a.m. of the following day after a night of sleep deprivation. The findings indicate that the differentiation was stable from morning to evening in all frequency bands, except in the delta band. However, after a night of sleep deprivation, the stability of the FCs was reduced. Consistent with this observation, the reduced differentiation following sleep deprivation was found to be negatively correlated with the effort perceived by participants in completing the cognitive task during sleep deprivation. This correlation suggests that individuals with less stable connectomes following sleep deprivation experienced greater difficulty in performing cognitive tasks, reflecting increased effort.

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“…Prolonged sleep deprivation further exacerbates these effects, with reduced activation in key areas like the prefrontal cortex, posterior parietal cortex, and supplementary motor area during working memory tasks. 105 While the exact nature of these changes – whether they are adaptive responses by the brain to cope with the lack of sleep or direct impairments caused by sleep deprivation – remains unclear, their significant impacts on cognition are evident.…”

Section: The Potential Mechanisms Driving Sd‐induced Pndmentioning

confidence: 99%

The influence of sleep disorders on perioperative neurocognitive disorders among the elderly: A narrative review

Chen,

Zhai,

Lan

et al. 2024

Ibrain

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This review comprehensively assesses the epidemiology, interaction, and impact on patient outcomes of perioperative sleep disorders (SD) and perioperative neurocognitive disorders (PND) in the elderly. The incidence of SD and PND during the perioperative period in older adults is alarmingly high, with SD significantly contributing to the occurrence of postoperative delirium. However, the clinical evidence linking SD to PND remains insufficient, despite substantial preclinical data. Therefore, this study focuses on the underlying mechanisms between SD and PND, underscoring that potential mechanisms driving SD‐induced PND include uncontrolled central nervous inflammation, blood–brain barrier disruption, circadian rhythm disturbances, glial cell dysfunction, neuronal and synaptic abnormalities, impaired central metabolic waste clearance, gut microbiome dysbiosis, hippocampal oxidative stress, and altered brain network connectivity. Additionally, the review also evaluates the effectiveness of various sleep interventions, both pharmacological and nonpharmacological, in mitigating PND. Strategies such as earplugs, eye masks, restoring circadian rhythms, physical exercise, noninvasive brain stimulation, dexmedetomidine, and melatonin receptor agonists have shown efficacy in reducing PND incidence. The impact of other sleep‐improvement drugs (e.g., orexin receptor antagonists) and methods (e.g., cognitive‐behavioral therapy for insomnia) on PND is still unclear. However, certain drugs used for treating SD (e.g., antidepressants and first‐generation antihistamines) may potentially aggravate PND. By providing valuable insights and references, this review aimed to enhance the understanding and management of PND in older adults based on SD.

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Reduced Resting-State EEG Power Spectra and Functional Connectivity after 24 and 36 Hours of Sleep Deprivation

Cited by 6 publications

References 88 publications

Effect of 24-h and 36-h Acute Total Sleep Deprivation on Human Attention: An Activation Likelihood Estimation Meta-analysis

Effect of 24-h and 36-h Acute Total Sleep Deprivation on Human Attention: An Activation Likelihood Estimation Meta-analysis

The Effect of Sleep Deprivation on Brain Fingerprint Stability: A Magnetoencephalography Validation Study

The influence of sleep disorders on perioperative neurocognitive disorders among the elderly: A narrative review

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