TY - JOUR
T1 - Orbitofrontal gray matter relates to early morning awakening: a neural correlate of insomnia complaints?
AU - Stoffers, D.
AU - Moens, S.
AU - Benjamins, J.
AU - van Tol, M.J.
AU - Penninx, B.W.J.H.
AU - Veltman, D.J.
AU - van der Wee, N.J.A.
AU - van Someren, E.J.W.
PY - 2012
Y1 - 2012
N2 - Sleep complaints increase profoundly with age; prevalence estimates of insomnia in the elderly reach up to 37%.The three major types of nocturnal complaints are difficulties initiating (DIS) and maintaining (DMS) sleep and early morning awakening (EMA), of which the latter appears most characteristic for aging. The neural correlates associated with these complaints have hardly been investigated, hampering the development of rational treatment and prevention. A recent study on structural brain correlates of insomnia showed that overall severity, but not duration, of insomnia complaints is associated with lower gray matter (GM) density in part of the left orbitofrontal cortex (OFC). Following up on this, we investigated, in an independent sample of people not diagnosed with insomnia, whether individual differences inGMdensity are associated with differences in DIS, DMS, and EMA. Sixty five healthy participants (mean ageD41 years, range 18-56) filled out questionnaires and underwent structural magnetic resonance imaging. Three compound Z-scores were computed for questionnaire items relating to DIS, DMS, and EMA.Whole-brain voxel-based morphometrywas used to investigate their association withGMdensity. Results showthat participants with lowerGMdensity in a region where the left inferior OFC borders the insula report more EMA, but not DIS or DMS.This is the first study to investigate structural brain correlates of specific sleep characteristics that can translate into complaints in insomniacs. The selective association of EMA with orbitofrontal GM density makes our findings particularly relevant to elderly people, where EMA represents the most characteristic complaint. It is hypothesized that low GM density in aforementioned orbitofrontal area affects its role in sensing comfort. An intact ability to evaluate comfort may be crucial to maintain sleep, especially at the end of the night when sleep is vulnerable because homeostatic sleep propensity has dissipated. © 2012 Stoffers, Moens, Ben-jamins, vanTol, Penninx, Veltman, Van der Wee and Van Someren.
AB - Sleep complaints increase profoundly with age; prevalence estimates of insomnia in the elderly reach up to 37%.The three major types of nocturnal complaints are difficulties initiating (DIS) and maintaining (DMS) sleep and early morning awakening (EMA), of which the latter appears most characteristic for aging. The neural correlates associated with these complaints have hardly been investigated, hampering the development of rational treatment and prevention. A recent study on structural brain correlates of insomnia showed that overall severity, but not duration, of insomnia complaints is associated with lower gray matter (GM) density in part of the left orbitofrontal cortex (OFC). Following up on this, we investigated, in an independent sample of people not diagnosed with insomnia, whether individual differences inGMdensity are associated with differences in DIS, DMS, and EMA. Sixty five healthy participants (mean ageD41 years, range 18-56) filled out questionnaires and underwent structural magnetic resonance imaging. Three compound Z-scores were computed for questionnaire items relating to DIS, DMS, and EMA.Whole-brain voxel-based morphometrywas used to investigate their association withGMdensity. Results showthat participants with lowerGMdensity in a region where the left inferior OFC borders the insula report more EMA, but not DIS or DMS.This is the first study to investigate structural brain correlates of specific sleep characteristics that can translate into complaints in insomniacs. The selective association of EMA with orbitofrontal GM density makes our findings particularly relevant to elderly people, where EMA represents the most characteristic complaint. It is hypothesized that low GM density in aforementioned orbitofrontal area affects its role in sensing comfort. An intact ability to evaluate comfort may be crucial to maintain sleep, especially at the end of the night when sleep is vulnerable because homeostatic sleep propensity has dissipated. © 2012 Stoffers, Moens, Ben-jamins, vanTol, Penninx, Veltman, Van der Wee and Van Someren.
U2 - 10.3389/fneur.2012.00105
DO - 10.3389/fneur.2012.00105
M3 - Article
SN - 1664-2295
VL - 3
SP - 10
JO - Frontiers in Neurology
JF - Frontiers in Neurology
M1 - 10
ER -