Back to Search Start Over

Sleep Arousal-Related Ventricular Repolarization Lability Is Associated With Cardiovascular Mortality in Older Community-Dwelling Men.

Authors :
Shahrbabaki, Sobhan Salari
Linz, Dominik
Redline, Susan
Stone, Katie
Ensrud, Kristine
Baumert, Mathias
Source :
CHEST. Feb2023, Vol. 163 Issue 2, p419-432. 14p.
Publication Year :
2023

Abstract

<bold>Background: </bold>Sleep is fragmented by brief arousals, and excessive arousal burden has been linked to increased cardiovascular (CV) risk, but mechanisms are poorly understood.<bold>Research Question: </bold>Do arousals trigger cardiac ventricular repolarization lability that may predispose people to long-term cardiovascular mortality?<bold>Study Design and Methods: </bold>This study analyzed 407,541 arousals in the overnight polysomnograms of 2,558 older men in the Osteoporotic Fractures in Men sleep study. QT and RR intervals were measured beat-to-beat starting 15 s prior to arousal onset until 15 s past onset. Ventricular repolarization lability was quantified by using the QT variability index (QTVi).<bold>Results: </bold>During 10.1 ± 2.5 years of follow-up, 1,000 men died of any cause, including 348 CV deaths. During arousals, QT and RR variability increased on average by 5 and 55 ms, respectively, resulting in a paradoxical transient decrease in QTVi from 0.07 ± 1.68 to -1.00 ± 1.68. Multivariable Cox proportional hazards analysis adjusted for age, BMI, cardiovascular and respiratory risk factors, sleep-disordered breathing and arousal, diabetes, and Parkinson disease indicated that excessive QTVi during arousal was independently associated with all-cause and CV mortality (all-cause hazard ratio, 1.20 [95% CI, 1.04-1.38; P = .012]; CV hazard ratio, 1.29 [95% CI, 1.01 -1.65; P = .043]).<bold>Interpretation: </bold>Arousals affect ventricular repolarization. A disproportionate increase in QT variability during arousal is associated with an increased all-cause and CV mortality and may reflect ventricular repolarization maladaptation to the arousal stimulus. Whether arousal-related QTVi can be used for more tailored risk stratification warrants further study, including evaluating whether arousal suppression attenuates ventricular repolarization lability and reduces subsequent mortality.<bold>Clinical Trial Registration: </bold>ClinicalTrials.gov; No.: NCT00070681; URL: www.<bold>Clinicaltrials: </bold>gov. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00123692
Volume :
163
Issue :
2
Database :
Academic Search Index
Journal :
CHEST
Publication Type :
Academic Journal
Accession number :
161488078
Full Text :
https://doi.org/10.1016/j.chest.2022.09.043