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. 2024 Nov 29;5(1):zpae087.
doi: 10.1093/sleepadvances/zpae087. eCollection 2024.

Comparison analysis between standard polysomnographic data and in-ear-electroencephalography signals: a preliminary study

Affiliations

Comparison analysis between standard polysomnographic data and in-ear-electroencephalography signals: a preliminary study

Gianpaolo Palo et al. Sleep Adv. .

Abstract

Study objectives: Polysomnography (PSG) currently serves as the benchmark for evaluating sleep disorders. Its discomfort makes long-term monitoring unfeasible, leading to bias in sleep quality assessment. Hence, less invasive, cost-effective, and portable alternatives need to be explored. One promising contender is the in-ear-electroencephalography (EEG) sensor. This study aims to establish a methodology to assess the similarity between the single-channel in-ear-EEG and standard PSG derivations.

Methods: The study involves 4-hour signals recorded from 10 healthy subjects aged 18-60 years. Recordings are analyzed following two complementary approaches: (1) a hypnogram-based analysis aimed at assessing the agreement between PSG and in-ear-EEG-derived hypnograms; and (2) a feature- and analysis-based on time- and frequency-domain feature extraction, unsupervised feature selection, and definition of Feature-based Similarity Index via Jensen-Shannon Divergence (JSD-FSI).

Results: We find large variability between PSG and in-ear-EEG hypnograms scored by the same sleep expert according to Cohen's kappa metric, with significantly greater agreements for PSG scorers than for in-ear-EEG scorers (p < .001) based on Fleiss' kappa metric. On average, we demonstrate a high similarity between PSG and in-ear-EEG signals in terms of JSD-FSI-0.79 ± 0.06-awake, 0.77 ± 0.07-nonrapid eye movement, and 0.67 ± 0.10-rapid eye movement-and in line with the similarity values computed independently on standard PSG channel combinations.

Conclusions: In-ear-EEG is a valuable solution for home-based sleep monitoring; however, further studies with a larger and more heterogeneous dataset are needed.

Keywords: in-ear-EEG; machine learning; multisource-scored sleep databases; sleep staging; sleep wearables.

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Conflict of interest statement

SUPSI authors are responsible for the research, and they conducted the analysis independently. IDUN Company representative contribution was in offering detailed information about the device and the dataset collected in a previous study. This study has been previously disseminated as a preprint on arXiv.

Figures

Figure 1.
Figure 1.
Schematic layout of the quality assurance study and the data collection procedure.
Figure 2.
Figure 2.
Devices employed in the data collection: (A) SOMNOmedics SOMNOscreen plus system for PSG data with the EXG configuration, that is, including six scalp electrodes, EOG, and ECG signal monitoring; (B) GDK hardware including ear tips, earpieces, and brain box used to record in-ear-EEG data.
Figure 3.
Figure 3.
Workflow for evaluating the similarity between the signals recorded from two different channels, including feature extraction and feature selection, separately for each sleep stage; and the comparison between feature distributions using the Jensen–Shannon divergence before the assessment of the similarity-scores, individually for each sleep stage and for each subject. In detail, (A) refers to the comparison between one in-ear-EEG and one PSG channel (either scalp-EEG or EOG channels); while (B) illustrates the analysis between two PSG channels (either scalp-EEG or EOG channels). An example of similarity-scores distribution for awake, NREM, and REM classes is included for both case studies.
Figure 4.
Figure 4.
(A) Intrascorer variability (multisource-scored dataset). Boxplot distribution of the Cohen’s kappa values computed for each recording/subject between the PSG and in-ear-EEG hypnograms—for each scorer. (B) Interscorer variability (multisource-scored dataset). Boxplot distributions of the Fleiss’ kappa values computed for each recording/subject between the three scorer experts for in-ear-EEG (in blue) and PSG (in red) signals.
Figure 5.
Figure 5.
Example of 30-second data samples from both PSG and in-ear EEG recordings, for each sleep stage. The PSG derivation considered is the C3-M2 channel.
Figure 6.
Figure 6.
JSD-FSI similarity scores distributions, that is, distributions derived from the PSG-to-in-ear-EEG (histograms in blue) and PSG-to-PSG (histograms in red) comparisons—for each subject in the awake stage.
Figure 7.
Figure 7.
JSD-FSI similarity-scores distributions, that is, distributions derived from the PSG-to-in-ear-EEG (histograms in blue) and PSG-to-PSG (histograms in red) comparisons—for each subject in the NREM sleep stage.
Figure 8.
Figure 8.
JSD-FSI similarity-scores distributions, that is distributions derived from the PSG-to-in-ear-EEG (histograms in blue) and PSG-to-PSG (histograms in red) comparisons—for each subject in the REM sleep stage. No JSD-FSI similarity scores are reported for subjects 3 and 8.

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