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Juvodden, H. T.

Publications and source records attributed to Juvodden, H. T..

2 recordsLinked to original sources

Optimizing automated sleep stage scoring of 5-second mini-epochs: a transfer learning study

Study objectiveConventional sleep staging relies on 30-second epochs, potentially concealing transient sleep stage intrusion and reducing precision. Building on our previous study of mini-epochs, we investigated whether U-Sleep, an existing automatic deep learning-based sleep staging model with high performance in epochs, could be optimized to similar performance level in 5-second mini-epoch scoring, thereby enabling more detailed sleep characterization. MethodsWe created a dataset of 48,000 human-scored 5-second mini-epochs from 100 PSGs. We compared mini-epochs to human-scored epochs before U-Sleep was optimized using transfer learning and evaluated on a test set. Model performance was assessed using F1-scores, confusion matrices, stage distributions and transition rates comparing scorings of the original U-Sleep before, and the optimized U-Sleep after transfer learning to human-scored mini-epochs. ResultsCompared to human-scored epochs, human-scored mini-epochs captured significantly more transitions (1.70/minute vs. 0.21/minute, p<0.001), and significantly more wake (8.4% versus 5.4%), N1 (7.2% versus 5.4%), and N2 (51.8% versus 40.9%), less N3 (15.4% versus 25.2%) and REM sleep (16.7% versus 23.0%) (all p<0.001). Optimizing U-Sleep improved its performance significantly from F1=0.74 to F1=0.81 (p<0.05) and gave increased transition rates in the test set (original U-Sleep: 1.06/minute, optimized U-Sleep: 1.34/minute, human-scored miniepochs: 1.70/minute). Stage distributions did not differ between optimized U-Sleeps scorings and human-scored mini-epochs. ConclusionsAfter optimization, U-Sleep performance in mini-epochs matched the high performance levels previously reported in both human and automated 30-second epoch scoring. This demonstrates the feasibility of precise, automated high resolution sleep staging. Future work should include external validation and application to full-night recordings. Statement of significanceConventional 30-second epochs limit temporal resolution in sleep staging and may conceal transient intrusions of wake or sleep stages. However, no validated methods are available for highresolution scoring. In this study, we trained and validated the state-of-the-art deep learning model U-Sleep for accurate automatic 5-second mini-epoch scoring using a large dataset of humanscored mini-epochs. The optimized model achieved a high performance, matching levels from previously reported automatic and human epoch scoring. Compared to epoch scoring, miniepochs captured significantly more stage transitions, supporting their ability to uncover sleep dynamics that are otherwise lost. Our findings show the potential of high-resolution sleep staging for more detailed characterization of sleep architecture and demonstrate the feasibility of precise, automatic mini-epoch scoring.

bioengineering↗

Narcolepsy type 1 patients have abnormal brain activation to neutral-rated movies in humor-paradigm

Narcolepsy type 1 is a neurological sleep disorder mainly characterized by excessive daytime sleepiness, fragmented night sleep, and cataplexy (muscle atonia triggered by emotions). To characterize brain activation patterns in response to neutral-rated and fun-rated movies in narcolepsy type 1 we performed functional magnetic resonance imaging during a paradigm consisting of 30 short movies (25/30 with a humorous punchline; 5/30 without a humorous punchline (but with similar build-up/anticipation)) that the participants rated based on their humor experience. We included 41 narcolepsy type 1 patients (31 females, mean age 23.6 years, 38/41 H1N1-vaccinated, 41/41 HLA-DQB1*06:02-positive, 40/40 hypocretin-deficient) and 44 first-degree relatives (24 females, mean age 19.6 years, 30/44 H1N1-vaccinated, 27/44 HLA-DQB1*06:02-positive) as controls. Group-level inferences were made using permutation testing.\n\nPermutation testing revealed no significant differences in the average ratings of patients and controls. Functional magnetic resonance imaging analysis revealed that both groups showed higher activations in response to fun-rated movies in several brain regions associated with humor processing, with no significant group differences. In contrast, patients showed significantly higher activation compared to controls during neutral-rated movies; including bilaterally in the thalamus, pallidum, putamen, amygdala, hippocampus, middle temporal gyrus, cerebellum, brainstem and in the left precuneus, supramarginal gyrus and caudate.\n\nThe presence of a humorous punchline in a neutral-rated movie is important since we found no brain overactivation for narcolepsy type 1 patients for movies without a humorous punchline (89.0% neutral-rated) compared with controls.\n\nFurther, a comparison between fun-rated and neutral-rated movies revealed a pattern of higher activation during fun-rated movies in controls, patients showed no significant differentiation between these states. Group analyses revealed significantly stronger differentiation between fun-rated and neutral-rated movies in controls compared with patients, including bilaterally in the inferior frontal gyrus, thalamus, putamen, precentral gyrus, lingual gyrus, supramarginal gyrus, occipital areas, temporal areas, cerebellum and in the right hippocampus, postcentral gyrus, pallidum and insula.\n\nIn conclusion, during neutral-rated movies, narcolepsy type 1 patients showed significantly higher activation in several cortical and subcortical regions previously implicated in humor and REM sleep, including the thalamus and basal ganglia. The relative lack of differentiation between neutral-rated and fun-rated movies in narcolepsy type 1 patients might represent insight into the mechanisms associated with cataplexy, in which a long-lasting hypervigilant state could represent risk (hypersensitivity to potential humorous stimuli) for the narcolepsy type 1 patients, which seem to have a lower threshold for activating the humor response, even during neutral-rated movies.

neuroscience↗