A scalable framework for population-level precision health: Insights from sleep disorders
Olive R Cawiding1, Dongyeop Kim2, Eun Yeon Joo3
1Biomedical Mathematics Group, Institute for Basic Science, Daejeon, 34126, Republic of Korea; Department of Mathematical Sciences, KAIST, Daejeon, 34141, Republic of Korea.
Sleep Medicine
|March 17, 2026
Summary
A machine learning tool, SLEEPS, assessed sleep disorder risks in over 40,000 users. It found obstructive sleep apnea risk increases with age, while insomnia risk showed minimal age association, highlighting digital health
Area of Science:
- Digital Health
- Machine Learning
- Sleep Medicine
Background:
- Assessing population-level sleep disorder risk is difficult due to biased samples and costly diagnostics.
- Traditional methods like hospital-based sampling and polysomnography have limitations for large-scale screening.
Purpose of the Study:
- To introduce SLEEPS, a machine learning algorithm for estimating population-level risks of insomnia, obstructive sleep apnea (OSA), and comorbid insomnia and sleep apnea (COMISA).
- To evaluate the performance and utility of SLEEPS using a large, web-based dataset.
Main Methods:
- Utilized SLEEPS, a machine learning algorithm, to analyze data from over 40,000 voluntary public users.
- Calculated total and isolated risks for insomnia and OSA.
- Compared web-based data with hospital-based samples to assess potential biases and differences.
Main Results:
- Total obstructive sleep apnea (OSA) risk increased significantly with age (τ∼0.453-0.465, p < 0.001).
- Total insomnia risk showed negligible association with age (|τ|<0.1, p < 0.001).
- Insomnia risk was higher in hospital samples compared to web samples, particularly in women, while OSA risk did not differ significantly.
Conclusions:
- SLEEPS offers a scalable, non-intrusive tool for population-level risk assessment of insomnia and OSA where polysomnography is impractical.
- This study demonstrates the potential of digital data and machine learning for evaluating chronic disease risk patterns in large populations.
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