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Sleep disorders affect billions worldwide, yet clinical polysomnography (PSG) analysis remains hindered by labor-intensive manual scoring and limited generalizability of automated sleep staging tools across heterogeneous protocols. We present LPSGM, a large-scale PSG model designed to address two critical challenges in sleep medicine: cross-center generalization and adaptable diagnosis of neuropsychiatric disorders. Trained on 220,500 hours of multi-center PSG data (24,000 full-night recordings from 16 public datasets), LPSGM integrates domain-adaptive pre-training, flexible channel configurations, and a unified architecture to mitigate variability in equipment, montages, and populations during sleep staging while enabling downstream fine-tuning for mental disorder detection. In prospective validation, LPSGM achieves expert-level consensus in sleep staging (κ = 0.845 ± 0.066 vs. inter-expert κ = 0.850 ± 0.102) and matches the performance of fully supervised models on two independent private cohorts. When fine-tuned, it attains 88.01% accuracy in narcolepsy detection and 100% accuracy in identifying major depressive disorder (MDD), highlighting shared physiological biomarkers between sleep architecture and neuropsychiatric symptoms. By bridging automated sleep staging with real-world clinical deployment, LPSGM establishes a scalable, data-efficient framework for integrated sleep and mental health diagnostics. The code and pre-trained model are publicly available at https://github.com/Deng-GuiFeng/LPSGM to advance reproducibility and translational research in sleep medicine.
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http://dx.doi.org/10.1101/2024.12.11.24318815 | DOI Listing |
J Safety Res
September 2025
School of Health and Biomedical Sciences, RMIT University, Australia; Institute for Breathing and Sleep, Austin Health, Heidelberg, Australia.
Introduction: Drowsiness is a significant cause of crashes in the various transport industries, including automotive, aviation, and rail. Our previous study investigated the differential induction of drowsiness in drivers caused by specific whole-body vibration (WBV) frequency ranges, with an amplitude of 0.2 m/s r.
View Article and Find Full Text PDFSci Adv
September 2025
Laboratory of Neurobiology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Acute sleep deprivation (SD) rapidly alleviates depression, addressing a critical gap in mood disorder treatment. Rapid eye movement SD (REM SD) modulates the excitability of vasoactive intestinal peptide (VIP) neurons, influencing the synaptic plasticity of pyramidal neurons. However, the precise mechanism remains undefined.
View Article and Find Full Text PDFFront Neurosci
August 2025
Beijing Life Science Academy, Beijing, China.
Hypocretin, also known as orexin, is a hypothalamic neuropeptide that regulates essential physiological processes including arousal, energy metabolism, feeding behavior, and emotional states. Through widespread projections and two G-protein-coupled receptors-HCRT-1R and HCRT-2R-the hypocretin system exerts diverse modulatory effects across the central nervous system. The role of hypocretin in maintaining wakefulness is well established, particularly in narcolepsy type 1 (NT1), where loss of hypocretin neurons leads to excessive daytime sleepiness and cataplexy.
View Article and Find Full Text PDFClin Kidney J
September 2025
Hypertension is a pervasive and progressive complication in chronic kidney disease (CKD) patients, affecting up to 90% of those in advanced stages or on dialysis. A particularly insidious aspect of this condition is nocturnal hypertension, characterized by high blood pressure (BP) during sleep and a blunted or absent nighttime BP dipping-phenomena associated with accelerated CKD progression and increased cardiovascular risk. Despite its strong prognostic significance, nocturnal hypertension remains underdiagnosed due to limited use of ambulatory BP monitoring.
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September 2025
Institute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Sleep is a complex behavior regulated by various brain cell types. However, the roles of brain-resident macrophages, including microglia and CNS-associated macrophages (CAMs), particularly those derived postnatally, in sleep regulation remain poorly understood. Here, we investigated the effects of resident (embryo-derived) and repopulated (postnatally derived) brain-resident macrophages on the regulation of vigilance states in mice.
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