STUDY OBJECTIVES: Although the stability of inter-individual differences in vulnerability to sleep deprivation has been shown behaviourally, the neural basis for these differences has yet to be uncovered. In this study, we assessed the reproducibility of fMRI activation and performance on a working memory task before and after 24 hours of sleep deprivation (SD). DESIGN: All volunteers underwent 2 sessions (pairs of fMRI scans) at rested wakefulness (RW) and after SD. PARTICIPANTS: 19 healthy, right-handed subjects (mean age = 21.37 +/- 1.54 years). MEASUREMENTS AND RESULTS: Brain activation was highly correlated across sessions in a frontoparietal network previously implicated in working memory function. The magnitude of decline in this activation after SD was preserved in bilateral parietal regions. Among several behavioural metrics investigated, the most robust marker of vulnerability to SD was the change in the intra-individual variability of reaction times. This was shown to be both stable over time and correlated with the drop in left parietal activation from RW to SD in both experimental sessions. CONCLUSIONS: Because of its reproducibility, the modulation of parietal activation may provide a good physiological marker of vulnerability to SD.
STUDY OBJECTIVES: Although the stability of inter-individual differences in vulnerability to sleep deprivation has been shown behaviourally, the neural basis for these differences has yet to be uncovered. In this study, we assessed the reproducibility of fMRI activation and performance on a working memory task before and after 24 hours of sleep deprivation (SD). DESIGN: All volunteers underwent 2 sessions (pairs of fMRI scans) at rested wakefulness (RW) and after SD. PARTICIPANTS: 19 healthy, right-handed subjects (mean age = 21.37 +/- 1.54 years). MEASUREMENTS AND RESULTS: Brain activation was highly correlated across sessions in a frontoparietal network previously implicated in working memory function. The magnitude of decline in this activation after SD was preserved in bilateral parietal regions. Among several behavioural metrics investigated, the most robust marker of vulnerability to SD was the change in the intra-individual variability of reaction times. This was shown to be both stable over time and correlated with the drop in left parietal activation from RW to SD in both experimental sessions. CONCLUSIONS: Because of its reproducibility, the modulation of parietal activation may provide a good physiological marker of vulnerability to SD.
Authors: Michael W L Chee; Jiat Chow Tan; Hui Zheng; Sarayu Parimal; Daniel H Weissman; Vitali Zagorodnov; David F Dinges Journal: J Neurosci Date: 2008-05-21 Impact factor: 6.167
Authors: Dean W Beebe; Mark W Difrancesco; Sarah J Tlustos; Kelly A McNally; Scott K Holland Journal: Behav Brain Funct Date: 2009-02-19 Impact factor: 3.759