ArticlemedRxiv : the preprint server for health sciences2025
Data-driven discovery of core sleep biomarkers for predicting early cardiometabolic risk in a healthy population using machine learning.
Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
Abstract
Background: Identifying robust biomarkers for future cardiometabolic risk within the crucial "preventive window" in healthy individuals remains a major challenge. While numerous sleep metrics are linked to health, their hierarchical importance is unknown. This study aimed to leverage a data-driven machine learning paradigm to move beyond conventional metrics and objectively identify the core sleep-related physiological drivers for predicting the transition to early-stage cardiometabolic risk. Methods: We conducted a longitudinal analysis on 447 initially healthy participants from the Sleep Heart Health Study (SHHS). A LASSO (L1-regularized) logistic regression model was trained on 16 high-quality clinical and polysomnographic features to perform data-driven biomarker selection, following a rigorous data quality audit where high-missingness variables (e.g., heart rate variability) were excluded. The performance of the final models was rigorously evaluated using 10-repeats of 10-fold cross-validation and compared using paired t-tests. Findings: LASSO regression identified a parsimonious set of six core predictors. Notably, respiratory disturbance index (RDI) and minimum nocturnal oxygen saturation (min_spo2) emerged as the key biomarkers, superseding traditional sleep fragmentation metrics like the arousal index. In the primary cross-validation analysis, the lean LASSO model demonstrated the strongest predictive performance (mean AUC = 0.698), statistically outperforming a complex model with all 16 features (mean AUC = 0.669, p<0.0001). This superiority and robustness were maintained in high-risk subgroups. Interpretation: Our data-driven approach reveals that physiological stress directly linked to sleep-disordered breathing and nocturnal hypoxemia, rather than general sleep fragmentation, are the primary drivers of the transition towards early cardiometabolic risk in healthy individuals. This finding provides specific, translatable targets for precision preventive medicine, points towards novel mechanisms for early risk development, and offers a blueprint for developing next-generation screening tools, potentially integrated into wearable technology.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.