Locus coeruleus microstructural integrity is associated with vigilance vulnerability to sleep deprivation

Insufficient sleep compromises cognitive performance, diminishes vigilance, and disrupts daily functioning in hundreds of millions of people worldwide. Despite extensive research revealing significant variability in vigilance vulnerability to sleep deprivation, the underlying mechanisms of these ind...

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Veröffentlicht in:Human brain mapping 2024-09, Vol.45 (13), p.e70013
Hauptverfasser: Quan, Peng, Mao, Tianxin, Zhang, Xiaocui, Wang, Ruosi, Lei, Hui, Wang, Jieqiong, Liu, Wanting, Dinges, David F, Jiang, Caihong, Rao, Hengyi
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Sprache:eng
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Zusammenfassung:Insufficient sleep compromises cognitive performance, diminishes vigilance, and disrupts daily functioning in hundreds of millions of people worldwide. Despite extensive research revealing significant variability in vigilance vulnerability to sleep deprivation, the underlying mechanisms of these individual differences remain elusive. Locus coeruleus (LC) plays a crucial role in the regulation of sleep-wake cycles and has emerged as a potential marker for vigilance vulnerability to sleep deprivation. In this study, we investigate whether LC microstructural integrity, assessed by fractional anisotropy (FA) through diffusion tensor imaging (DTI) at baseline before sleep deprivation, can predict impaired psychomotor vigilance test (PVT) performance during sleep deprivation in a cohort of 60 healthy individuals subjected to a rigorously controlled in-laboratory sleep study. The findings indicate that individuals with high LC FA experience less vigilance impairment from sleep deprivation compared with those with low LC FA. LC FA accounts for 10.8% of the variance in sleep-deprived PVT lapses. Importantly, the relationship between LC FA and impaired PVT performance during sleep deprivation is anatomically specific, suggesting that LC microstructural integrity may serve as a biomarker for vigilance vulnerability to sleep loss.
ISSN:1065-9471
1097-0193
1097-0193
DOI:10.1002/hbm.70013