98%
921
2 minutes
20
Objective: Prognostication in patients with disorders of consciousness (DOCs) remains challenging because of heterogeneous etiologies, pathophysiologies and, consequently, highly variable electroencephalograms (EEGs). Here, we use EEG patterns that are well-characterizable to create a latent map that positions novel EEGs along a continuum. We asses this map as a generalizable tool to extract prognostically valuable information from long-term EEG, by predicting outcome post-cardiac arrest as a first use case.
Methods: Categorizable EEGs across the health-disease continuum (wake [W], sleep [rapid eye movement (REM), non-REM (N1, N2, N3)], ictal-interictal-continuum [lateralized and generalized periodic discharges (LPD, GPD) and lateralized and generalized rhythmic delta activity (LRDA, GRDA)], seizures [SZ], burst suppression [BS]; 20,043 patients, 288,986 EEG segments) are arranged meaningfully in a low-dimensional space via a deep neural network, resulting in a universal map of EEG (UM-EEG). We assess prognostication after cardiac arrest (576 patients, recovery or death) based on long-term EEGs represented as trajectories in this continuous embedding space.
Results: Classification of out-of-sample EEG match state-of-the-art artificial intelligence algorithms while extending it to the currently largest set of classes across the health-disease continuum (mean area under the receiver-operating-characteristic curve [AUROCs] 1-vs-all classification: W, 0.94; REM, 0.92; N1, 0.85; N2, 0.91; N3, 0.98; GRDA, 0.97; LRDA, 0.97; SZ, 0.87; GPD, 0.99; LPD, 0.97; BS, 0.94). UM-EEG enables outcome prediction after cardiac arrest with an AUROC of 0.86 and identifies interpretable factors governing prognosis such as the distance to healthy states over time.
Interpretation: UM-EEG presents a novel and physiologically meaningful representation to characterize brain states along the health-disease continuum. It offers new opportunities for personalized, long-term monitoring and prognostication. ANN NEUROL 2025;98:357-368.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12278028 | PMC |
http://dx.doi.org/10.1002/ana.27260 | DOI Listing |
Nat Med
July 2025
Department of Computer Science and Applied Mathematics, Weizmann Institute of Science, Rehovot, Israel.
The Human Phenotype Project (HPP) is a large-scale deep-phenotype prospective cohort. To date, approximately 28,000 participants have enrolled, with more than 13,000 completing their initial visit. The project is aimed at identifying novel molecular signatures with diagnostic, prognostic and therapeutic value, and at developing artificial intelligence (AI)-based predictive models for disease onset and progression.
View Article and Find Full Text PDFAnn Neurol
August 2025
Computational Neurology, Department of Neurology and Berlin Institute of Health, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Objective: Prognostication in patients with disorders of consciousness (DOCs) remains challenging because of heterogeneous etiologies, pathophysiologies and, consequently, highly variable electroencephalograms (EEGs). Here, we use EEG patterns that are well-characterizable to create a latent map that positions novel EEGs along a continuum. We asses this map as a generalizable tool to extract prognostically valuable information from long-term EEG, by predicting outcome post-cardiac arrest as a first use case.
View Article and Find Full Text PDFNat Commun
April 2025
Centre for Organismal Studies (COS), Heidelberg University, Heidelberg, Germany.
The polygenic contribution to heart development and function along the health-disease continuum remains unresolved. To gain insight into the genetic basis of quantitative cardiac phenotypes, we utilize highly inbred Japanese rice fish models, Oryzias latipes, and Oryzias sakaizumii. Employing automated quantification of embryonic heart rates as core metric, we profiled phenotype variability across five inbred strains.
View Article and Find Full Text PDFiScience
March 2025
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
In an era where established lines between cell identities are blurred by intra-lineage plasticity, distinguishing stable from transitional states is critical, especially within Group 1 ILCs, where similarity and plasticity between NK cells and ILC1s obscure their unique contributions to immunity. This study leverages AsGM1-a membrane lipid associated with cytotoxic attributes absent in ILC1s-as a definitive criterion to discriminate between these cell types. Employing this glycosphingolipid signature, we achieved precise delineation of Group 1 ILC diversity across tissues.
View Article and Find Full Text PDFEur J Prev Cardiol
November 2024
Jessa Hospital, Department of Cardiology and Jessa & Science, Hasselt, Belgium.
Aims: Low cardiorespiratory fitness (CRF) is associated with functional disability, heart failure and mortality. Left ventricular (LV) end-diastolic volume (LVEDV) has been linked with CRF, but its utility as a diagnostic marker of low CRF has not been tested.
Methods: This multi-center international cohort examined the relationship between LV size on echocardiography and CRF (peak oxygen uptake [peak VO2] from cardiopulmonary exercise testing) in individuals with LV ejection fraction ≥50%.