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人工智能自动检测发作间期癫痫样放电:方法进展、临床评价与神经发育背景

Front Cell Dev Biol · 2026年9月8日 · Ma 等 6 位作者

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一分钟了解要点综述 AI 自动识别癫痫样放电的评价方法,提出多中心验证与人在回路框架。结果文章强调应明确目标事件、匹配规则、记录时长和用途,并报告灵敏度、精确率、假阳性负担等。

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摘要Abstract

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Interictal epileptiform discharges (IEDs) are established electroencephalographic biomarkers that support epilepsy diagnosis and characterization, but their visual identification is time-consuming and subject to inter-rater variability. This review critically examines automated IED analysis from rule-based systems to contemporary deep learning, with particular attention to task definition, validation design, and clinical workflow. We use the term "accuracy paradox" as an author-defined descriptive label-not as an established field-wide concept-for the mismatch between high performance on presegmented epochs or recording-level classification and the temporal and spatial precision required for event-level interpretation. Accuracy, area under the curve, F1 score, concordance, and false positives per hour quantify different aspects of performance and should not be treated as interchangeable. Clinical evaluation should therefore specify the target event, temporal and spatial matching rules, recording duration, annotated event count, validation level, and intended use, while reporting sensitivity, precision, F1 score, false-positive burden, and workflow outcomes as appropriate. We also discuss neurodevelopmental and cellular mechanisms that may influence network excitability, including neuroinflammation, complement-associated synaptic remodeling, and chloride homeostasis. Available evidence supports biological plausibility but does not establish that AI-derived IED morphology can reveal molecular states in individual patients. We propose a translational framework based on independent multicenter validation, context-specific operating thresholds, robust evaluation of explanations, and human-in-the-loop triage. Prospective studies integrating scalp or intracranial EEG with spatially matched surgical tissue and single-cell or spatial transcriptomic profiling could test macro-to-molecular hypotheses, but these applications remain investigational.

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