The Relative Contributions of Arousal Presence and Arousal Intensity to Post-Respiratory-Event Ventilation in Obstructive Sleep Apnea

Study ObjectivesObstructive sleep apnea (OSA) exhibits cyclical patterns of respiratory events followed by hyperpneic breaths which frequently coincide with arousals. While this hyperventilation partially results from accumulated respiratory stimuli, arousal (i.e., its presence and intensity) appears to contribute independently. As such, this study aims to quantify the relative contributions of arousal presence and intensity to post-event ventilation independent of chemoreflex-driven responses. MethodsThis study utilized two retrospective polysomnography (PSG) data sets, comprising a community-based (Multi-Ethnic Study of Atherosclerosis, MESA, N=1781) and the Physiological Study data set (N=67). Arousal presence (0/1), arousal intensity (range 0-9), and post-event ventilation were calculated for each respiratory obstructive event for all participants using computational models. Mixed-effects linear models were used to examine the association between arousal presence and intensity, and post-event ventilation at both inter-event and inter-participant levels. ResultsAt the inter-event level, arousal presence at respiratory event termination increased ventilation by 17-30%Eupnea (increase above eupneic baseline) in both data sets, where each step increment in arousal intensity contributed an additional 1-4%Eupnea increase in ventilation. At the inter-participant level, each step increment of overnight mean arousal intensity was associated with 2-4%Eupnea increase in ventilatory response to arousal in both data sets. ConclusionsOur findings demonstrate that arousal presence plays an essential role in elevating post-event hyperventilation in OSA, with arousal intensity exerting modest influence per increment, but substantial cumulative effects at moderate-high levels. These results, consistent across both data sets, suggest a distinct mechanistic pathway to post-event hyperventilation beyond chemoreflex stimulation.