SLEEP 2011 Abstract Supplement
SLEEP 2011 Abstract Supplement
SLEEP 2011 Abstract Supplement
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A. Basic Science XI. Sleep Deprivation<br />
Conclusion: Extended “recovery” sleep over the weekend reverses the<br />
impact of one work-week of mild sleep restriction on sleepiness but<br />
does not improve performance suggesting that complete performance<br />
recovery may require more that just two days. In addition, it appears that<br />
increased SWS in women compared to men protects them from the effect<br />
of sleep loss on sleepiness and performance impairment, whereas it<br />
enhances recovery from these effects of modest sleep loss.<br />
0275<br />
EFFECTS OF <strong>SLEEP</strong> DEPRIVATION ON NEURAL<br />
CORRELATES OF RISK-TAKING<br />
Rao H 1,2,3,4 , Luftig D 2 , Lim J 2 , Detre JA 1 , Dinges DF 2<br />
1<br />
Center for Functional Neuroimaging, Department of Neurology<br />
and Radiology, University of Pennsylvania, Philadelphia, PA, USA,<br />
2<br />
Division of Sleep & Chronobiology, Department of Psychiatry,<br />
University of Pennsylvania, Philadelphia, PA, USA, 3 Center<br />
for Functional Brain Imaging, South China Normal University,<br />
Guangzhou, China, 4 Department of Psychology, Sun Yat-Sen<br />
University, Guangzhou, China<br />
Introduction: Sleep deprivation (SD) can induce significant deficits in<br />
vigilant attention, working memory, and executive function. However,<br />
the effects of SD on risk-taking behavior are unclear, with some studies<br />
reporting greater risk-taking behavior while others reporting no changes<br />
following sleep loss. The present study used functional MRI with a<br />
modified balloon analog risk task (BART) paradigm and examined the<br />
effects of 24h of total sleep deprivation (TSD) on the neural correlates<br />
of risk-taking.<br />
Methods: A total of 27 healthy adults (13 male) were scanned on a Siemens<br />
3T Trio scanner while performing a modified BART task at rested<br />
baseline (BL) and after 24h of TSD, using a standard EPI sequence.<br />
During the BART, subjects were required to sequentially inflate a virtual<br />
balloon that could either grow larger or explode. Imaging data were<br />
analyzed by SPM5.<br />
Results: Behavioral data showed no changes of risk-taking propensity<br />
from BL to SD (6.5 vs. 6.6, p>.7). Imaging data showed robust activation<br />
in the mesolimbic, frontal, and visual pathway areas during the<br />
BART both at BL and during SD, which replicated our previous studies.<br />
Direct comparisons between these brain activation patterns indicated no<br />
differences from BL to SD. However, direct comparisons between the<br />
neural responses to the loss events (balloon explosion) showed reduced<br />
activation in the left insula. Furthermore, at BL, both SPM whole brain<br />
analysis and independent ROI analysis showing that insular and striatum<br />
activation level negatively correlated with risk-taking propensity, which<br />
also replicated our previous finding. However, such negative correlations<br />
were not found after SD.<br />
Conclusion: Consistent with literature, our data showed that 24h of<br />
TSD did not change risk-taking behavior. However, significantly reduced<br />
activation in the insula was observed during loss events following<br />
TSD, which may reflect diminished negative emotional response to loss<br />
outcomes during risk-taking. Moreover, the loss of negative correlations<br />
between risk-taking behavior and activation level in insular and<br />
striatum following TSD, suggesting that one night sleep loss can alter<br />
neural mechanisms mediating inter-individual differences in risk-taking<br />
propensity without actual behavioral changes. Overall, our data suggest<br />
that sleep loss alters neural responses associated with risk-taking and<br />
support the hypothesis that neuroimaging findings may be a precursor to<br />
the behavioral changes following long-term sleep deprivation.<br />
Support (If Any): This study is supported by Air Force Office of Scientific<br />
Research Grant FA9550-05-1-0293, NIH Grant R01 HL102119;<br />
in part by the National Space Biomedical Research Institute through<br />
NASA NCC 9-58; and in part by NIH Grants CTRC UL1RR024134<br />
and P30 NS045839.<br />
0276<br />
DIFFERENTIAL EFFECTS OF TOTAL <strong>SLEEP</strong> DEPRIVATION<br />
ON REGIONAL CORTICAL ACTIVITY AT REST<br />
AND DURING PSYCHOMOTOR VIGILANCE TEST<br />
PERFORMANCE<br />
Rao H 1,2,3,4 , Lim J 2 , Zhu S 1,4 , Wu W 1 , Hu S 1,2 , Detre JA 1 , Dinges DF 2<br />
1<br />
Center for Functional Neuroimaging, Department of Neurology<br />
and Radiology, University of Pennsylvania, Philadelphia, PA, USA,<br />
2<br />
Division of Sleep & Chronobiology, Department of Psychiatry,<br />
University of Pennsylvania, Philadelphia, PA, USA, 3 Center<br />
for Functional Brain Imaging, South China Normal University,<br />
Guangzhou, China, 4 Department of Psychology, Sun Yat-Sen<br />
University, Guangzhou, China<br />
Introduction: Sleep deprivation (SD) degrades multiple aspects of neurocognitive<br />
performance. With few exceptions, recent neuroimaging<br />
studies have reported hypo-activation in fronto-parietal regions during<br />
various tasks following sleep loss. However, most of these studies focused<br />
on the effects of SD on task-induced neural activation, while the<br />
effects of SD on resting brain function without task requirements remain<br />
unexplored. The present study used arterial spin labeling (ASL) perfusion<br />
fMRI and examined the effects of 24h of total SD on brain function<br />
at rest and during a psychomotor vigilance test (PVT).<br />
Methods: A total of 31 healthy adults (16 male) were scanned on a Siemens<br />
3T Trio scanner at non-task resting states and during the PVT after<br />
normal sleep and after 24h of TSD, using a a pseudo-continuous ASL<br />
sequence. Data were analyzed by SPM5. One mean resting CBF image<br />
was generated for each condition from each subject before and after<br />
TSD. Whole brain general linear modeling analysis was conducted.<br />
Results: TSD significantly disrupted PVT performance (p