% 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{Schnakenberg:893852,
author = {Schnakenberg, Patricia and Hahn, Lisa and Stickel, Susanne
and Stickeler, Elmar and Habel, Ute and Eickhoff, Simon B.
and Chechko, Natalia and Dukart, Juergen},
title = {{E}xamining early structural and functional brain
alterations in postpartum depression through multimodal
neuroimaging},
journal = {Scientific reports},
volume = {11},
number = {1},
issn = {2045-2322},
address = {[London]},
publisher = {Macmillan Publishers Limited, part of Springer Nature},
reportid = {FZJ-2021-02876},
pages = {13551},
year = {2021},
abstract = {Postpartum depression (PPD) affects approximately 1 in 10
women after childbirth. A thorough understanding of a
preexisting vulnerability to PPD will likely aid the early
detection and treatment of PPD. Using a within-sample
association, the study examined whether the brain's
structural and functional alterations predict the onset of
depression. 157 euthymic postpartum women were subjected to
a multimodal MRI scan within the first 6 days of childbirth
and were followed up for 12 weeks. Based on a clinical
interview 12 weeks postpartum, participants were classified
as mentally healthy or having either PPD or adjustment
disorder (AD). Voxel-based morphometry and resting-state
functional connectivity comparisons were performed between
the three groups. $13.4\%$ of women in our study developed
PPD (n = 21) and $12.1\%$ (n = 19) adjustment disorder (AD).
The risk factors for PPD were a psychiatric history and the
experience and severity of baby blues and the history of
premenstrual syndrome. Despite the different risk profiles,
no differences between the PPD, AD and control group were
apparent based on structural and functional neuroimaging
data immediately after childbirth. At 12 weeks postpartum, a
significant association was observed between Integrated
Local Correlation (LCor) and the Edinburgh Postnatal
Depression Score (EPDS). Our findings do not support the
notion that the brain's structural and resting-state
functional alterations, if present, can be used as an early
biomarker of PPD or AD. However, effects may become apparent
if continuous measures of symptom severity are chosen.},
cin = {INM-7 / INM-10},
ddc = {600},
cid = {I:(DE-Juel1)INM-7-20090406 / I:(DE-Juel1)INM-10-20170113},
pnm = {5252 - Brain Dysfunction and Plasticity (POF4-525)},
pid = {G:(DE-HGF)POF4-5252},
typ = {PUB:(DE-HGF)16},
pubmed = {34193913},
UT = {WOS:000671789900004},
doi = {10.1038/s41598-021-92882-w},
url = {https://juser.fz-juelich.de/record/893852},
}