Proposition of a new, minimally-invasive, software smartphone device to predict sleep apnea and its severity
- PMID: 40911165
- PMCID: PMC12413423
- DOI: 10.1007/s11325-025-03441-w
Proposition of a new, minimally-invasive, software smartphone device to predict sleep apnea and its severity
Abstract
Purpose: obstructive sleep apnea is underdiagnosed due to limited access to polysomnography (PSG). We aimed to assess the performances of Apneal®, an application recording sound and movements thanks to a smartphone's microphone, accelerometer and gyroscope, to estimate patients' apnea-hypopnea index (AHI).
Methods: monocentric proof-of-concept study with a first manual scoring step, then automatic detection of respiratory events from recorded signals using a sequential deep-learning model (version 0.1 of Apneal® automatic scoring of respiratory events, end 2022), in adult patients.
Results: 46 patients (women 34%, BMI 28.7 kg/m²) were included. Sensitivity of manual scoring was 0.91 (95% CI [0.8-1]) for IAH > 15 and 0.85 [0.67-1] for AHI > 30, and positive predictive values (PPV) 0.89 [0.76-0.97] and 0.94 [0.8-1]. We obtained an AUC-ROC of 0.85 (95% CI [0.69-0.96]) and AUC-PR of 0.94 (95% CI [0.84-0.99]) for the identification of AHI > 15, and AUC-ROC of 0.95 [0.860.99] and AUC-PR of 0.93 [0.81-0.99] for AHI > 30. The ICC between the AHI estimated manually, and from the PSG is 0.89 (p = 6.7 × 10- 17), Pearson correlation 0.90 (p = 1.25 × 10- 17). Automatic scoring found sensitivity of 1 [0.95-1], PPV of 0.9 [0.8-0.9] for AHI > 15, and sensitivity 0.95 [0.84-1], PPV 0.69 [0.52-0.85] for AHI > 30. The ICC between the estimated AHI, and PSG scorings is 0.84 (p = 5.4 × 10- 11) and Pearson correlation is 0.87 (p = 1.7 × 10- 12).
Conclusion: Manual scoring of smartphone-based signals is possible and accurate compared to PSG-based scorings. Automatic scoring method based on a deep learning model provides promising results.
Trial registration: NCT03803098.
Keywords: Artificial intelligence; Deep learning; Diagnosis; Sleep apnea; Smartphone.
© 2025. The Author(s).
Conflict of interest statement
Declaration. Ethical approval: All procedures performed in studies involving human participants were in accordance with the ethical standards of the Jardé law in France and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study. Ethical Approval was obtained from Comité de Protection des Personnes Sud Est VI (approval number AU 1443). Conflict of interest: Justine Frija is the PI of the EASY study, funded by Mitral SA and EIT Health. Juliette Millet is an employee of Mitral. Emilie Béquignon has no COI. Ala Covali has no COI. Guillaume Cathelain is an employee of Mitral. Josselin Houenou has no COI. Hélène Benzaquen has no COI. Pierre A. Geoffroy has no COI. Emmanuel Bacry has no COI. Mathieu Grajoszex has no COI. Marie-Pia d’Ortho has no COI.
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