% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Schiel:1009296,
author = {Schiel, Julian E and Tamm, Sandra and Holub, Florian and
Petri, Roxana and Dashti, Hassan S and Domschke, Katharina
and Feige, Bernd and Goodman, Matthew O and Jones, Samuel E
and Lane, Jacqueline M and Ratti, Pietro-Luca and Ray, David
W and Redline, Susan and Riemann, Dieter and Rutter, Martin
K and Saxena, Richa and Sexton, Claire E and Tahmasian,
Masoud and Wang, Heming and Weedon, Michael N and Weihs,
Antoine and Kyle, Simon D and Spiegelhalder, Kai},
title = {{A}ssociations between sleep health and grey matter volume
in the {UK} {B}iobank cohort ( {N} = 33,356)},
journal = {Brain communications},
volume = {5},
number = {4},
issn = {2632-1297},
address = {[Großbritannien]},
publisher = {Guarantors of Brain},
reportid = {FZJ-2023-02746},
pages = {fcad200},
year = {2023},
abstract = {As suggested by previous research, sleep health is assumed
to be a key determinant of future morbidity and mortality.
In line with this, recent studies have found that poor sleep
is associated with impaired cognitive function. However, to
date, little is known about brain structural abnormalities
underlying this association. Although recent findings link
sleep health deficits to specific alterations in grey matter
volume, evidence remains inconsistent and reliant on small
sample sizes.Addressing this problem, the current
preregistered study investigated associations between sleep
health and grey matter volume (139 imaging-derived
phenotypes) in the UK Biobank cohort (33,356 participants).
Drawing on a large sample size and consistent data
acquisition, sleep duration, insomnia symptoms, daytime
sleepiness, chronotype, sleep medication, and sleep apnoea
were examined.Our main analyses revealed that long sleep
duration was systematically associated with larger grey
matter volume of basal ganglia substructures. Insomnia
symptoms, sleep medication and sleep apnoea were not
associated with any of the 139 imaging-derived phenotypes.
Short sleep duration, daytime sleepiness as well as late and
early chronotype were associated with solitary
imaging-derived phenotypes (no recognizable pattern, small
effect sizes).To our knowledge, this is the largest study to
test associations between sleep health and grey matter
volume. Clinical implications of the association between
long sleep duration and larger grey matter volume of basal
ganglia are discussed. Insomnia symptoms as operationalised
in the UK Biobank do not translate into grey matter volume
findings.},
cin = {INM-7},
ddc = {610},
cid = {I:(DE-Juel1)INM-7-20090406},
pnm = {5252 - Brain Dysfunction and Plasticity (POF4-525)},
pid = {G:(DE-HGF)POF4-5252},
typ = {PUB:(DE-HGF)16},
pubmed = {37492488},
UT = {WOS:001036190500001},
doi = {10.1093/braincomms/fcad200},
url = {https://juser.fz-juelich.de/record/1009296},
}