TY - JOUR
T1 - White matter microstructural properties are related to inter-individual differences in cognitive instability after sleep deprivation
AU - Zhu, Yuanqiang
AU - Wang, Liuxian
AU - Xi, Yibin
AU - Dai, Tian
AU - Fei, Ningbo
AU - Liu, Lin
AU - Xu, Ziliang
AU - Yang, Xuejuan
AU - Fu, Chang
AU - Sun, Jinbo
AU - Xu, Junling
AU - Shi, Dapeng
AU - Tian, Jie
AU - Yin, Hong
AU - Qin, Wei
N1 - Publisher Copyright:
© 2017 IBRO
PY - 2017/12/4
Y1 - 2017/12/4
N2 - Several diseases are characterized by cognitive instability, which is amplified in the conditions of sleep deprivation (SD). Cognitive instability in SD can be examined by the number of lapses on the psychomotor vigilance test (PVT), which is considered to be a gold standard in the field. However, the number of PVT lapses widely range according to inter-individual differences, from apparent cognitive resistance to severe cognitive impairment. In this study, tract-based spatial statistical analyses with multiple diffusion tensor imaging-derived characteristics (i.e., fractional anisotropy (FA), mean diffusivity, radial diffusivity, and axial diffusivity) were employed to investigate the relationships between the number of PVT lapses and the diffusion characteristics. A hierarchical linear regression model was then used to assess the contributions of tract-specific FA values in predicting PVT lapses. Finally, dichotomized analysis was used to investigate white matter (WM) differences between resilient and vulnerable groups. Our results showed significant negative correlations between numbers of PVT lapses and FA in multiple WM tracts, with the FA variations in the superior longitudinal fasciculus and splenium of the corpus callosum accounting for nearly 37.5% of individual variability in PVT lapses. In addition, dichotomized analyses indicated that the resilient participants exhibited significantly higher FA values compared with the vulnerable participants. Together, these findings suggest that cognitive instability after SD was closely associated with individual differences in WM integrity.
AB - Several diseases are characterized by cognitive instability, which is amplified in the conditions of sleep deprivation (SD). Cognitive instability in SD can be examined by the number of lapses on the psychomotor vigilance test (PVT), which is considered to be a gold standard in the field. However, the number of PVT lapses widely range according to inter-individual differences, from apparent cognitive resistance to severe cognitive impairment. In this study, tract-based spatial statistical analyses with multiple diffusion tensor imaging-derived characteristics (i.e., fractional anisotropy (FA), mean diffusivity, radial diffusivity, and axial diffusivity) were employed to investigate the relationships between the number of PVT lapses and the diffusion characteristics. A hierarchical linear regression model was then used to assess the contributions of tract-specific FA values in predicting PVT lapses. Finally, dichotomized analysis was used to investigate white matter (WM) differences between resilient and vulnerable groups. Our results showed significant negative correlations between numbers of PVT lapses and FA in multiple WM tracts, with the FA variations in the superior longitudinal fasciculus and splenium of the corpus callosum accounting for nearly 37.5% of individual variability in PVT lapses. In addition, dichotomized analyses indicated that the resilient participants exhibited significantly higher FA values compared with the vulnerable participants. Together, these findings suggest that cognitive instability after SD was closely associated with individual differences in WM integrity.
KW - cognitive instability
KW - diffusion tensor imaging
KW - individual difference
KW - psychomotor vigilance test
KW - sleep deprivation
UR - https://www.scopus.com/pages/publications/85032224407
U2 - 10.1016/j.neuroscience.2017.09.047
DO - 10.1016/j.neuroscience.2017.09.047
M3 - 文章
C2 - 28987509
AN - SCOPUS:85032224407
SN - 0306-4522
VL - 365
SP - 206
EP - 216
JO - Neuroscience
JF - Neuroscience
ER -