Biology subjects

Blume, C.

Publications and source records attributed to Blume, C..

16 recordsLinked to original sources

bioRxiv2026

A single day of natural daylight exposure and physical activity does not conclusively change circadian phase: A Bayesian crossover experiment

Among the environmental signals that shape human physiology, the daily light-dark cycle is the primary zeitgeber of the human circadian system. Physical activity may provide an additional non-photic time cue and frequently co-occurs with daylight in everyday life. However, their independent and combined effects on circadian phase have rarely been disentangled under naturalistic daylight conditions. In a counterbalanced mixed-design experiment, 41 healthy adults (24 women; mean age = 23.7 years, SD = 4.3) participated in up to three 40-h visits on fixed individual sleep-wake schedules. Each visit comprised an 8-h exposure beginning 1.5 h after wake to natural daylight, daylight attenuated by amber-tinted glasses, or indoor electric light (within subjects; mean photopic illuminances: 1196, 460, and 75 lx), with otherwise dim-light conditions. Participants hiked for approximately 4 h or remained sedentary (between subjects; activity indexed by median heart rate reserve [HRR]; group means: 32.7% and 2.7%). Bayesian hierarchical models used individual photopic illuminance (ActTrust 2) and median HRR to predict change in dim-light melatonin onset (DLMO; primary outcome) and exploratory outcomes (daytime and evening sleepiness, mood, and wellbeing, daytime perceived exertion, and evening psychomotor vigilance). Per standard-deviation increase in log-transformed illuminance and median HRR, estimated DLMO changes were -4.22 min (95% HDI [-10.93, 2.22]; BF = 0.70) and -6.48 min (95% HDI [-13.79, 1.27], BF = 1.56), respectively. Evidence remained inconclusive for both predictors and their interaction. Exploratory findings were largely inconclusive, practically negligible, or favoured the absence of effects. The circadian effects of a single day of natural daylight exposure, with or without physical activity, therefore remain unclear. Resolving this question may require larger samples and brighter, repeated, or habitual exposure timed to phases of greater circadian light sensitivity.

neuroscience↗

bioRxiv2026

Associations between habitual light exposure-related behaviors and sleep timing and sleep complaints in an international community sample

Sleep is essential for health and light is an important environmental signal influencing its timing, quality, and regulation. Retinal light exposure reflects the interplay between environmental illumination and behavioral choices, yet it remains unclear which habitual light exposure-related behaviors meaningfully impact sleep outcomes. In this preregistered analysis, we examined associations between these behaviors, sleep timing, and sleep complaints in a large, international community sample (N = 774, Mage = 32.6 {+/-} 14.6 years). Participants completed the Light Exposure Behavior Assessment (LEBA), with four behavioral domains included in the analyses. Sleep timing, sleep disturbances and sleep-related daytime impairment were measured using established questionnaires. Bayesian analyses indicated that time spent outdoors and device use in bed were most strongly associated with sleep outcomes. Greater time outdoors was linked to earlier sleep timing and fewer sleep complaints, whereas more frequent device use in bed was associated with greater sleep disturbance and daytime impairment. Morning and daytime lighting practices and evening light control showed no conclusive evidence. Together, these findings highlight the relevance of everyday light exposure-related behaviors for sleep and support behavioral approaches to promoting healthy sleep in real-world contexts.

neuroscience↗

bioRxiv2025

Spring Fatigue is a Cultural Phenomenon rather than a Seasonal Syndrome

Although not as prominent as in other animals, also humans experience seasonal variations in for example sleep duration and circadian processes. These variations are likely primarily driven by changes in photoperiod length. Anecdotally, a relevant number of people report experiencing fatigue and low energy levels particularly during spring - at least in Germany, Switzerland, and Austria. Thus, this phenomenon is commonly referred to as "spring fatigue". However, scientific evidence for such a seasonal syndrome is largely missing. We thus investigated temporal variations in fatigue, daytime sleepiness, insomnia symptoms, and sleep quality through an online survey including repeated (i.e., every six weeks) assessments of the same individuals over the course of one year. We hypothesised that fatigue and daytime sleepiness would be higher during shorter photoperiods. We further expected lower sleep quality and more severe insomnia symptoms under shorter photoperiods. Additionally, we explored variations with photoperiod change, across months, and seasons. Hypotheses were tested using Bayesian linear mixed-effects models. The study and analyses were pre-registered. Between April 2024 and September 2025, 418 adults (80% women) completed at least two assessments. Nearly half of participants (47 %) reported experiencing spring fatigue. However, repeated assessments across one year showed no evidence for seasonal or monthly variations in fatigue, sleepiness, insomnia symptoms, or sleep quality. Fatigue during day-to-day activities decreased with longer photoperiods but was independent of photoperiod change. Overall, the results provide evidence against spring fatigue as a genuine seasonal phenomenon. The discrepancy between high self-reports of the phenomenon and stable longitudinal patterns suggests that spring fatigue may reflect cultural labelling and result from cognitive-perceptual biases rather than reflecting a genuine seasonal syndrome.

animal behavior and cognition↗

bioRxiv2024

Reduced and Redundant: Information Processing of Prediction Errors during Sleep

During sleep, the human brain transitions to a sentinel processing mode, enabling the continued processing of environmental stimuli despite the absence of consciousness. Here, we employed advanced information-theoretic analyses, including mutual information (MI) and co-information (co-I), alongside event-related potential (ERP) and temporal generalization analyses (TGA), to characterize auditory prediction error processing across wakefulness and sleep. We hypothesized that a shared neural code would be present across sleep stages, with deeper sleep being associated with reduced information content and increased information redundancy. To investigate this, twenty-nine young healthy participants were exposed to an auditory local-global oddball paradigm during wakefulness and during an 8-hour sleep opportunity monitored via polysomnography in a cross-sectional study. We focused on local mismatch responses to a deviating fifth tone following four standard tones. ERP analyses showed that prediction error processing continued throughout all sleep stages (N1-N3, REM). Mutual information analyses revealed a substantial reduction in the amount of encoded prediction error information particularly during N3 and REM, although ERP amplitudes increased with deeper NREM sleep. In addition, we observed delayed information encoding during sleep and co-information analyses showed that neural dynamics became increasingly redundant with increasing sleep depth. Temporal generalisation analyses revealed a largely shared neural code between N2 and N3 sleep, although it differed between wakefulness and sleep. Here, we showed how the neural code of the sentinel processing mode changes from wake to light to deep sleep and REM, characterised by delayed processing, more redundant and less rich neural information in the human cortex as consciousness wanes. This altered stimulus processing reveals how neural information changes with the changes of consciousness states as we traverse the night.

neuroscience↗

bioRxiv2024

From womb to crib: How fetal activity patterns in utero reveal postnatal sleep behavior

ImportanceThe human circadian system, a critical biological mechanism governing the sleep-wake cycle, begins to oscillate before birth. Distinct fetal behavioral states have been described using short-duration ultrasound recordings, but the alignment of fetal activity with day and night cycles (i.e., diurnal rhythms) remains poorly understood due to the lack of long-term monitoring. Accordingly, a substantial knowledge gap exists concerning the evolution of fetal diurnal rhythms into infant sleep-wake cycles. ObjectiveTo investigate the development of fetal diurnal rhythms and their evolution into postnatal infant sleep, as well as the role of maternal factors and melatonin in shaping early circadian entrainment. MethodsIn this cohort study, conducted in 2022 and 2023, we collected over 20 000 hours of wearable acceleration and temperature data from 32 fetuses and their mothers during continuous 5-day monitoring in the third trimester of pregnancy. The cohort was subsequently followed longitudinally from the prenatal period through 6 months postpartum, with infant sleep outcomes assessed at three key time points (first postnatal weeks, 3 months, and 6 months) using sleep diaries and questionnaires. The first postnatal assessment additionally included breast milk and infant stool sample collection. ResultsMulti-level modelling revealed early diurnal rhythms in fetuses that align with maternal activity and circadian rhythms. Random Forest analyses identified fetal day/night sleep duration ratio - a simplified proxy for fetal circadian entrainment - as the strongest predictor of postnatal infant sleep, with fetuses preferring nighttime sleep maintaining this preference postnatally. Maternal sleep regularity (i.e., consistent sleep patterns characterized by low day-to-day variability in sleep timing) during pregnancy also predicted infant sleep, associating with a stronger preference for nighttime sleep in infants. Conclusions and relevanceThese findings highlight the potential influence of intrauterine and maternal factors on the evolution of circadian entrainment. Our study contributes to a broader understanding of the earliest emergence of circadian rhythms, supporting future research on their long-term health impacts. Maternal sleep regularity stands out as the earliest modifiable target for interventions, offering an actionable pathway to promote infant circadian entrainment, with potential long-term benefits for family dynamics and well-being.

developmental biology↗

bioRxiv2024

Cardiac responses to auditory irregularities reveal hierarchical information processing during sleep

Our ability to process environmental stimuli varies during sleep. Although much research focused on neural processing, emerging evidence shows that bodily signals may play a key role in understanding high-level sensory processing during sleep. Here, we tested how cardiac responses to the local-global paradigm, a typical oddball task probing the processing of simple (local) and complex (global) sensory irregularities. To do so, we analyzed electrocardiography (ECG) signals in a total of 56 participants from two existing datasets which contained cerebral responses to local auditory irregularities, but which did not analyze the ECG data before. We found that cardiac activity slowed down after global, but not local, auditory irregularities, revealing the presence of global deviance effect in Rapid Eye Movement (REM) sleep. In contrast, cardiac activity was faster after local, but not global, deviants in Non-Rapid Eye Movement (NREM) sleep. Overall, our results demonstrate that cardiac responses to auditory irregularities inform about hierarchical information processing and its variations during sleep beyond cerebral activity. They highlight the embodiment of cognitive function and the value of cardiac signals to understand the variations of sensory processing during sleep.

neuroscience↗

bioRxiv2024

Somatic gene delivery for flexible in vivo modeling of high-risk sarcoma

A particular challenge hampering therapeutic advancements for high-risk sarcoma patients is the broad spectrum of molecularly distinct sarcoma entities and the corresponding lack of suitable model systems to recapitulate and study these diseases. To overcome this predicament, we developed a novel genetically-controlled, yet versatile mouse modeling platform allowing delivery of different genetic lesions by electroporation (EPO) of the thigh muscle wildtype mice. This optimized sarcoma EPO-GEMM (EPO-based genetically engineered mouse model) platform allowed the generation of ten biologically distinct sarcoma entities, including Synovial Sarcoma (SS), fusion-positive and fusion-negative Rhabdomyosarcoma (RMS), Alveolar Soft Part Sarcoma (ASPS), Undifferentiated Pleomorphic Sarcoma (UPS) and Infantile Fibrosarcoma (IFS). Comprehensive molecular profiling and cross-species analyses confirmed faithful recapitulation of the human disease, including the expression of relevant immunotherapy targets. Syngeneic allografting enabled reliable preservation and scalability of Sarcoma-EPO-GEMMs for treatment trials, such as B7-H3-directed CAR-T cell therapy in an immunocompetent background.

cancer biology↗

bioRxiv2023

Effects of calibrated blue-yellow (-S+) changes in light on the human circadian clock

Evening exposure to short-wavelength light can acutely affect the circadian clock located in the suprachiasmatic nuclei, sleep, and alertness. The intrinsically photosensitive retinal ganglion cells (ipRGCs) expressing the photopigment melanopsin are thought to be the primary drivers of these effects. Much less is known about the contribution of the colour-sensitive cones. Using calibrated silent-substitution changes in light colour along the blue-yellow axis, we investigated whether mechanisms of colour vision affect the human circadian system and sleep. In a 32.5-h repeated within-subjects protocol, 16 healthy participants (8 women, 18-35 years old) were exposed to three different light scenarios for 1 h starting 30 min after habitual bedtime: a control condition ("background", 93.5 photopic lux), intermittently flickering yellow-bright light (1 Hz, 30s on-off, 123.5 photopic lux), and intermittently flickering blue-dim light (1 Hz, 30s on-off; 67.0 photopic lux). Importantly, there was no difference in melanopsin excitation (163.2{+/-}2.1 lux melanopic EDI) between the three lighting conditions, allowing us to determine the unique contribution of the blue-yellow colour system. Our analyses did not yield conclusive evidence for differences between the three lighting conditions regarding circadian melatonin phase delays, melatonin suppression, subjective sleepiness, psychomotor vigilance, or sleep. Thus, in this study, we found no evidence that evening light changing along the blue-yellow dimension under moderate light levels typical for room illumination has a major impact on the human circadian clock or sleep. Our work underscores the previously demonstrated primary role of melanopsin-containing ipRGCs in mediating these effects.

neuroscience↗

bioRxiv2022

Light targeting the melanopic system suppresses melatonin, but does not alter sleepiness, vigilance, sensory processing, or sleep

Pre-sleep exposure to short-wavelength light suppresses melatonin and decreases sleepiness with activating effects extending to sleep. This has mainly been attributed to melanopic effects, but mechanistic insights are missing. Thus, we investigated whether two light conditions only differing in the melanopic effects (123 vs. 59 lux melanopic EDI) differentially affect sleep besides melatonin. Additionally, we studied whether the light differentially modulates sensory processing during wakefulness and sleep. Twenty-nine healthy volunteers (18-30 years, 15 women) were exposed to two metameric light conditions (high-vs. low-melanopic, {approx}60 photopic lux) for 1 hour ending 50 min prior to habitual bed time. This was followed by an 8-h sleep opportunity with polysomnography. Objective sleep measurements were complemented by self-report. Salivary melatonin, subjective sleepiness, and behavioural vigilance were sampled at regular intervals. Sensory processing was evaluated during light exposure and sleep on the basis of neural responses related to violations of expectations in an oddball paradigm. We observed suppression of melatonin by {approx}14 % in the high-compared to the low-melanopic condition. However, conditions did not differentially affect sleep, sleep quality, sleepiness, or vigilance. A neural mismatch response was evident during all sleep stages, but not differentially modulated by light. Suppression of melatonin by light targeting the melanopic system does not automatically translate to acutely altered levels of vigilance or sleepiness or to changes in sleep, sleep quality, or basic sensory processing. Given contradicting earlier findings and the retinal anatomy, this may suggest that an interaction between melanopsin and cone-rod signals needs to be considered. Statement of SignificanceMetameric light allows to mechanistically investigate the contribution of one specific retinal receptor. Using this approach, we here investigated the effects of high-vs. low-melanopic light for 1 hour in the evening at ecologically valid screen illuminance ({approx}60 photopic lux). Going beyond earlier research, we also investigated effects on sleep. We found that despite significant suppression of melatonin, other endpoints including sleep and sleep quality were not differentially affected. This underlines that melatonin suppression does not automatically translate to alterations of sleep, sleepiness, or vigilance. Further, it suggests that melanopsin effects may need to be studied in the context of cone-rod signals. Future research should thus investigate the relevance of such an interaction, which may vary between endpoints.

neuroscience↗

bioRxiv2021

The brain tunes to unfamiliar voices during sleeping

The brain continues to respond selectively to environmental stimuli even during sleep. However, the functional role of such responses, and whether they reflect information processing or rather sensory inhibition is not fully understood. Here, we presented 17 human sleepers (14 females) with their own name and two unfamiliar first names, spoken by either a familiar voice (FV) or an unfamiliar voice (UFV), while recording polysomnography during a full nights sleep. We detected K-complexes, sleep spindles, and micro-arousals, and then assessed event-related potentials, oscillatory power as well as intertrial phase synchronization in response to the different stimuli presented during non-rapid eye movement (NREM) sleep. We show that UFVs evoke more K-complexes and micro-arousals than FVs. When both stimuli evoke a K-complex, we observed larger evoked potentials, higher oscillatory power in the high beta (>16Hz) frequency range, and stronger time-locking in the delta band (1-4 Hz) in response to UFVs relative to FVs. Crucially, these differences in brain responses disappear when no K-complexes are evoked by the auditory stimuli. Our findings highlight discrepancies in brain responses to auditory stimuli based on their relevance to the sleeper and propose a key role for K-complexes in the modulation of sensory processing during sleep. We argue that such content-specific, dynamic reactivity to external sensory information enables the brain to enter a sentinel processing mode in which it engages in the many important processes that are ongoing during sleep while still maintaining the ability to process vital information in the surrounding. Significance statementPrevious research has shown that sensory processing continues during sleep. Here, we studied the capacity of the sleeping brain to extract and process relevant sensory information. We presented sleepers with their own names and unfamiliar names spoken by either a familiar (FV) or an unfamiliar voice (UFV). During non-rapid eye movement (NREM) sleep, UFVs elicited more K-complexes and micro-arousals than FVs. By contrasting stimuli which evoked K-complexes, we demonstrate that UFVs triggered larger evoked potentials, stronger time-locking in the delta (1-4Hz) band, and higher oscillatory power (>16Hz) relative to FVs. These differences in brain responses disappeared when no K-complexes were evoked. Our results suggest a pivotal role for K-complexes in the selective processing of relevant information during NREM sleep.

neuroscience↗

bioRxiv2021

Integrated phospho-proteogenomic and single-cell transcriptomic analysis of meningiomas establishes robust subtyping and reveals subtype-specific immune invasion

Meningiomas are the most frequent primary intracranial tumors. They can follow a wide clinical spectrum from benign to highly aggressive clinical course. No specific therapy exists for refractory cases or cases not amenable to resection and radiotherapy. Identification of risk of recurrence and malignant transformation for the individual patients is challenging. However, promising molecular markers and prognostic subgrouping by DNA methylation are emerging. Still, the biological underpinnings of these diagnostic subgroups are elusive, and, consequently, no novel therapeutic options arise thereof. Here we establish robust subgroups across the full landscape of meningiomas, consistent through DNA methylation, mutations, the transcriptomic, proteomic and phospho-proteomic level. Pronounced proliferative stress and DNA damage repair signals in malignant cells and in clusters exclusive to recurrent tumors are in line with their higher mitotic activity, but also provide an explanation for the accumulation of genomic instability in anaplastic meningiomas. Although homozygous deletion of CDKN2A/B is a diagnostic marker of high-grade meningioma, the expression of its gene product increased from low to non-deleted high-grade cases. Differences between subgroups in lymphocyte and myeloid cell infiltration, representing a majority of tumor mass in low-grade NF2 tumors, could be assigned to cluster-specific interaction with tumor cells. Activation to a more proinflammatory phenotype and decreased infiltration of myeloid cells in high-grade cases correlated with lower expression of CSF1, located on chromosome arm 1p, whose deletion is known as prognostic marker, with no proposed mechanism before. Our results demonstrate a robust molecular subclassification of a tumor type across multiple layers, provide insight into heterogeneous growth dynamics despite shared pathognomonic mutations, and highlight immune infiltration modulation as a novel target for meningioma therapy.

genomics↗

bioRxiv2021

Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial ependymoma

Ependymomas encompass a heterogeneous group of central nervous system (CNS) neoplasms that occur along the entire neuroaxis. In recent years, extensive (epi-)genomic profiling efforts have identified several molecular groups of ependymoma that are characterized by distinct molecular alterations and/or patterns. Based on unsupervised visualization of a large cohort of genome-wide DNA methylation data, we identified a highly distinct group of pediatric-type tumors (n = 40) forming a cluster separate from all established CNS tumor types, of which a high proportion were histopathologically diagnosed as ependymoma. RNA sequencing revealed recurrent fusions involving the pleomorphic adenoma gene-like 1 (PLAGL1) gene in 19 of 20 of the samples analyzed, with the most common fusion being EWSR1:PLAGL1 (n = 13). Five tumors showed a PLAGL1:FOXO1 fusion and one a PLAGL1:EP300 fusion. High transcript levels of PLAGL1 were noted in these tumors, with concurrent overexpression of the imprinted genes H19 and IGF2, which are regulated by PLAGL1. Histopathological review of cases with sufficient material (n = 16) demonstrated a broad morphological spectrum of largely ependymoma-like tumors. Immunohistochemically, tumors were GFAP-positive and OLIG2- and SOX10-negative. In 3/16 of the cases, a dot-like positivity for EMA was detected. Consistent with other fusion-positive ependymal groups, all tumors in our series were located in the supratentorial compartment. Median age of the patients at the time of diagnosis was 6.2 years. Analysis of time to progression or recurrence revealed survival times comparable to those of patients with ZFTA:RELA-fused ependymoma. In summary, our findings suggest the existence of a novel group of supratentorial ependymomas that are characterized by recurrent PLAGL1 fusions and enriched for pediatric patients.

cancer biology↗

bioRxiv2020

A novel isoform of ACE2 is expressed in human nasal and bronchial respiratory epithelia and is upregulated in response to RNA respiratory virus infection

Angiotensin-converting enzyme 2 (ACE2) is the main entry point in the airways for SARS-CoV-2. ACE2 binding to SARS-CoV-2 protein Spike triggers viral fusion with the cell membrane, resulting in viral RNA genome delivery into the host. Despite ACE2s critical role in SARS-CoV-2 infection, an understanding of ACE2 expression, including in response to viral infection, remains unclear. Until now ACE2 was thought to encode five transcripts and one 805 amino acid protein. Here we identify a novel short isoform of ACE2. Short ACE2 is expressed in the airway epithelium, the main site of SARS-CoV-2 infection; it is substantially upregulated in response to interferon stimulation and RV infection, but not in response to SARS-CoV-2 infection, and it shows differential regulation in asthma patients. This short isoform lacks SARS-CoV-2 spike glycoprotein high-affinity binding sites and altogether, our data are consistent with a model where short ACE2 may influence host susceptibility to SARS-CoV-2 infection.

molecular biology↗

bioRxiv2020

Transparency and open science reporting guidelines in sleep research and chronobiology journals

"Open science" is an umbrella term describing various aspects of transparent and open science principles. The adoption of open science principles at different levels of the scientific process (e.g., individual researchers, laboratories, institutions) has been rapidly changing the scientific research landscape in the past years, but uptake of these principles differ from discipline to discipline. Here, we asked to what extent journals in the field of sleep and chronobiology research encourage or even require following transparent and open science principles in their author guidelines. To this end, we scored the author guidelines of a comprehensive set of 28 sleep and chronobiology journals, including the major outlets in the field, using the standardised Transparency and Openness (TOP) Factor. This instrument rates the extent to which journals encourage or require following various aspects of open science, including data citation, data transparency, analysis code transparency, materials transparency, design and analysis guidelines, study pre-registration, analysis plan pre-registration, replication, registered reports, and the use of open science badges. Across the 28 journals, we find low values on the TOP Factor (median [25th, 75th percentile] 2.5 [1, 3], min. 0, max. 9, out of a total possible score of 28). This suggests an opportunity for sleep and chronobiology journals to further support the recent developments by implementing transparency and openness principles in their guidelines and making adherence to them mandatory.

scientific communication and education↗

bioRxiv2019

Actigraphy in brain-injured patients - A valid measurement for assessing circadian rhythms?

BackgroundActigraphy has received increasing attention in classifying rest-activity cycles. However, in patients with disorders of consciousness (DOC), actigraphy data may be considerably confounded by passive movements, such as nursing activities and therapies. Consequently, this study verified whether circadian rhythmicity is (still) visible in actigraphy data from patients with DOC after correcting for passive movements. MethodsWrist actigraphy was recorded over 7-8 consecutive days in patients with DOC (diagnosed with unresponsive wakefulness syndrome [UWS; n=19] and [exit] minimally conscious state [MCS/EMCS; n=11]). Presence and actions of clinical and research staff as well as visitors were indicated using a tablet in the patients room. Following removal and interpolation of passive movements, non-parametric rank-based tests were computed to identify differences between circadian parameters of uncorrected and corrected actigraphy data. ResultsUncorrected actigraphy data overestimated the interdaily stability and intradaily variability of patients activity and underestimated the deviation from a circadian 24h rhythm. Only 5/30 (17%) patients deviated more than 1h from 24h in the uncorrected data, whereas this was the case for 17/30 (57%) patients in the corrected data. When contrasting diagnoses based on the corrected dataset, stronger circadian rhythms and higher activity levels were observed in MCS/EMCS as compared to UWS patients. Day-to-night differences in activity were evident for both patient groups. ConclusionOur findings indicate that uncorrected actigraphy data overestimates the circadian rhythmicity of patients activity, as nursing activities, therapies, and visits by relatives follow a circadian pattern itself. Therefore, we suggest correcting actigraphy data from patients with reduced mobility.

neuroscience↗

bioRxiv2017

Standing Sentinel during Sleep: Continued Evaluation of Environmental Stimuli in the Absence of Consciousness

While it is a well-established finding that subjects own names (SON) or familiar voices are salient during wakefulness, we here investigated processing of environmental stimuli during sleep including deep N3 and REM sleep. Besides the effects of sleep depth we investigated how sleep-specific EEG patterns (i.e. sleep spindles and slow oscillations [SOs]) relate to stimulus processing. Using 256-channel EEG we studied processing of auditory stimuli by means of event-related oscillatory responses (de-/ synchronisation, ERD/ERS) and potentials (ERPs) in N = 17 healthy sleepers. We varied stimulus salience by manipulating subjective (SON vs. unfamiliar name) and paralinguistic emotional relevance (familiar vs. unfamiliar voice, FV/UFV). Results reveal that evaluation of voice familiarity continues during all NREM sleep stages and even REM sleep suggesting a sentinel processing mode of the human brain in the absence of wake-like consciousness. Especially UFV stimuli elicit larger responses in a 1-15 Hz range suggesting they continue being salient. Beyond this, we find that sleep spindles and the negative slope of SOs attenuate information processing. However, unlike previously suggested they do not uniformly inhibit information processing, but inhibition seems to be scaled to stimulus salience.\n\nFundingCB is supported by the Konrad-Adenauer-Stiftung e.V. and CB, MW and DPJH are supported by a grant from the Austrian Science Fund FWF (Y-777). CB, RdG, MW and DPJH are also supported by the Doctoral College \"Imaging the Mind\" (FWF; W1233-G17).

neuroscience↗