A sleep spindle detection algorithm that emulates human expert spindle scoring.

J Neurosci Methods

Center for Advanced Research in Sleep Medicine, Centre de Recherche de l'Hôpital du Sacré-Cœur de Montréal, Montréal, QC, Canada; Département de Psychiatrie, Université de Montréal, Montréal, QC, Canada. Electronic address:

Published: March 2019


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Article Abstract

Background: Sleep spindles are a marker of stage 2 NREM sleep that are linked to learning & memory and are altered by many neurological diseases. Although visual inspection of the EEG is considered the gold standard for spindle detection, it is time-consuming, costly and can introduce inter/ra-scorer bias.

New Method: Our goal was to develop a simple and efficient sleep-spindle detector (algorithm #7, or 'A7') that emulates human scoring. 'A7' runs on a single EEG channel and relies on four parameters: the absolute sigma power, relative sigma power, and correlation/covariance of the sigma band-passed signal to the original EEG signal. To test the performance of the detector, we compared it against a gold standard spindle dataset derived from the consensus of a group of human experts.

Results: The by-event performance of the 'A7' spindle detector was 74% precision, 68% recall (sensitivity), and an F1-score of 0.70. This performance was equivalent to an individual human expert (average F1-score = 0.67).

Comparison With Existing Method(s): The F1-score of 'A7' was 0.17 points higher than other spindle detectors tested. Existing detectors have a tendency to find large numbers of false positives compared to human scorers. On a by-subject basis, the spindle density estimates produced by A7 were well correlated with human experts (r = 0.82) compared to the existing detectors (average r = 0.27).

Conclusions: The 'A7' detector is a sensitive and precise tool designed to emulate human spindle scoring by minimizing the number of 'hidden spindles' detected. We provide an open-source implementation of this detector for further use and testing.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415669PMC
http://dx.doi.org/10.1016/j.jneumeth.2018.08.014DOI Listing

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