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Amino acid identified associated with poor performance under sleep restriction

Findings advance ability to predict an individual's performance under 5 consecutive nights of 4 hours in bed

Date:
June 10, 2016
Source:
University of Pennsylvania School of Medicine
Summary:
The amino acid acetylcarnitine may help predict an individual's neurobehavioral performance during chronic sleep restriction, according to new results.
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The amino acid acetylcarnitine may help predict an individual's neurobehavioral performance during chronic sleep restriction, according to results of a new study (abstract 0251) from researchers at the Perelman School of Medicine at the University of Pennsylvania that will be presented at SLEEP 2016, the 30th annual meeting of the Associated Professional Sleep Societies LLC.

Previous studies have shown that sleep loss degrades behavioral attention, cognitive processing and memory, but this study offers the first experimental evidence that acetylcarnitine -- which transports fatty acids into the mitochondria where they are broken down and oxidized and formed into energy -- may predict neurobehavioral vulnerability to sleep loss in healthy adults.

In the study at the sleep lab at the Hospital of the University of Pennsylvania, participants' blood samples were taken after 10-12 hours of fasting following one night of baseline sleep (10 hours time in bed), chronic sleep restriction (5 consecutive nights of 4 hours time in bed), and one night of recovery sleep (12 hours time in bed).

The Psychomotor Vigilance Test (PVT), the Digit Symbol Substitution Task (DSST), the Digit Span Task (DS), the Karolinska Sleepiness Scale (KSS) and the Profile of Mood States (POMS) tests were administered every two hours while participants were awake.

The preliminary data associated acetylcarnitine with six neurobehavioral variables during sleep loss, including PVT lapses (longer than 500 millisecond responses) and errors, PVT response speed, DSST total correct, DS total correct, KSS scores, and POMS vigor scores -- but not at baseline or recovery. Higher levels of this molecule predicted poorer behavioral attention, slower ability to process information, and poorer memory and increased sleepiness.

"We know that there are robust differences in how individuals respond to sleep loss," said Namni Goel, PhD, a research associate professor of psychology in Psychiatry in the division of Sleep and Chronobiology, and lead author on the study. "Some people are very vulnerable, while others are more resistant to these effects. Identifying this marker is an important step in identifying measures to mitigate the disruptive effects of sleep loss in those who are more affected."

The findings have implications for government agencies and other institutions interested in predicting who may be vulnerable to sleep loss and finding ways to offset the negative effects of sleep loss when they occur.

These data build on earlier work by members of the Penn team, who previously found two markers of sleep debt that reliably track when a person is sleep deprived (Weljie et al 2015, PNAS 112(8):2569-74).


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University of Pennsylvania School of Medicine. "Amino acid identified associated with poor performance under sleep restriction: Findings advance ability to predict an individual's performance under 5 consecutive nights of 4 hours in bed." ScienceDaily. ScienceDaily, 10 June 2016. <www.sciencedaily.com/releases/2016/06/160610173608.htm>.
University of Pennsylvania School of Medicine. (2016, June 10). Amino acid identified associated with poor performance under sleep restriction: Findings advance ability to predict an individual's performance under 5 consecutive nights of 4 hours in bed. ScienceDaily. Retrieved May 26, 2017 from www.sciencedaily.com/releases/2016/06/160610173608.htm
University of Pennsylvania School of Medicine. "Amino acid identified associated with poor performance under sleep restriction: Findings advance ability to predict an individual's performance under 5 consecutive nights of 4 hours in bed." ScienceDaily. www.sciencedaily.com/releases/2016/06/160610173608.htm (accessed May 26, 2017).

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