Hippocampal gray matter volume alterations in patients with first-episode and recurrent major depressive disorder and their associations with gene profiles
Fenfen Sun,
No information about this author
Yifan Shuai,
No information about this author
Jingru Wang
No information about this author
et al.
BMC Psychiatry,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: Feb. 15, 2025
Recent
studies
indicate
that
patients
with
first-episode
drug-naïve
(FEDN)
and
recurrent
major
depressive
disorder
(R-MDD)
exhibit
distinct
atrophy
patterns
in
the
hippocampal
subregions
along
proximal-distal
axis.
However,
it
remains
unclear
whether
such
differences
occur
long
axis
how
they
may
relate
to
specific
genes.
In
present
study,
we
analyzed
T1-weighted
images
from
421
(FEDN:
n
=
232;
R-MDD:
189)
544
normal
controls
(NC)
as
part
of
REST-meta-MDD
consortium.
Additionally,
transcriptome
maps
structural
Magnetic
Resonance
Imaging
(MRI)
data
six
donated
brains
were
obtained
Allen
Human
Brain
Atlas
(AHBA).
We
first
identified
changes
gray
matter
volume
(GMV)
within
hippocampus
both
FEDN
R-MDD
then
integrated
these
findings
AHBA
investigate
genes
associated
GMV
changes.
Compared
NC,
displayed
reduced
left
tail,
whereas
exhibited
decreased
bilateral
body
increased
tail.
Further
analysis
revealed
expression
levels
SYTL2
positively
correlated
patients,
while
SORCS3
SLIT2
those
R-MDD.
Our
results
suggest
alterations
subfields
differ
between
R-MDD,
reflecting
progressive
deterioration
prolonged
depression,
potentially
supported
by
These
offer
valuable
insights
into
neural
genetic
mechanisms
underlying
which
aid
development
more
targeted
effective
treatment
strategies
for
MDD
subtypes.
Language: Английский
Cerebral perfusion and gray matter volume alterations associated with cognitive impairment in metabolic syndrome with cerebral small vessel disease
Han Liu,
No information about this author
Wenhui Zheng,
No information about this author
Jie Geng
No information about this author
et al.
Frontiers in Aging Neuroscience,
Journal Year:
2025,
Volume and Issue:
17
Published: April 22, 2025
Objective
Metabolic
syndrome
(MetS)
combined
with
cerebral
small
vessel
disease
(CSVD)
is
associated
cognitive
dysfunction.
However,
the
underlying
mechanisms
remain
poorly
understood.
This
study
investigated
roles
of
brain
perfusion
and
gray
matter
volume
(GMV)
in
dysfunction
patients
MetS
CSVD
(MetS-CSVD).
Methods
enrolled
180
86
healthy
controls
(HCs).
Patients
were
categorized
into
without
(MetS-NCSVD)
(
n
=
58)
(MetS-CSVD)
122)
groups.
All
participants
underwent
laboratory
tests,
neuropsychological
assessments,
3D
pseudo-continuous
arterial
spin
labeling
(3D-PCASL),
magnetic
resonance
imaging
scans
voxel-based
morphometry
(VBM).
Cerebral
blood
flow
(CBF),
GMV,
clinical
scales
analyzed
for
correlations
regions
interest
(ROIs).
The
relationships
among
performance,
CBF,
GMV
evaluated
using
partial
correlation
analysis
multivariable
linear
regression
(MLRA).
Mediation
was
performed
to
investigate
CBF
association
between
scores
performance.
Results
Compared
MetS-NCSVD
HC
groups,
MetS-CSVD
group
displayed
significantly
reduced
frontal
temporal
lobes.
Partial
revealed
that
frontotemporal
lobe
strongly
overall
function,
executive
language
function
group.
MLRA
identified
score
as
sole
independent
factor
negatively
lobes
mediated
relationship
function.
Conclusion
CSVD,
rather
than
individual
components
MetS,
impairment
MetS-CSVD.
likely
contributes
indirectly
through
its
effects
on
these
patients.
Language: Английский