Objective: This study aimed to shed light on the potential relationships between blood volatile organic compounds (VOCs) and sleep health as well as mortality.
Methods: We employed generalized linear (GL), restricted cubic spline (RCS), weighted quantile sum (WQS), quantile-based g-calculation (QGC), and Bayesian kernel machine regression (BKMR) models to assess the relationship between blood VOCs-including bromoform (NHANES code: LBXVBF), bromodichloromethane (LBXVBM), chloroform (LBXVCF), dibromochloromethane (LBXVCM), and methyl tert-butyl ether (LBXVME)-and sleep health indicators (trouble sleeping, sleep disorders, and insufficient (< 6 h/day) or excessive (> 9 h/day) sleep) in participants from the NHANES 2007-2012. The Cox proportional hazards regression model was also used for survival analysis.
Results: The baseline profile categorized by sex showed that women had a higher prevalence of trouble sleeping, whereas men were more prone to insufficient sleep. We did not observe significant linear-correlations between VOCs and both increased sleep duration and poor sleep patterns, as shown by the weighted linear/logistic regression models. The RCS regression model indicated significant non-linear relationships (P for non-linear < 0.05) between certain VOC and sleep health. Adjusted QGC analysis highlighted LBXVBF as a crucial factor related to poor sleep quality (weighted 0.733). The BKMR analysis showed a positive trend between VOC levels (55th to 75th percentiles) and poor sleep pattern. Furthermore, the adjusted COX-RCS analysis identified LBXVME (P for non-linear = 0.0359) as a risk factor for all-cause mortality.
Conclusions: This study investigated the non-linear association between VOC exposure and sleep function, suggesting that VOC exposure may be linked to poor sleep patterns among U.S. adults.
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