Meditsinskiy sovet = Medical Council,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 6, 2024
Depression
is
a
clinically
significant
and
growing
public
health
issue.
As
major
global
disease
burden,
its
prevalence
has
been
steadily
increasing
over
the
years,
affecting
different
demographic
groups.
Depressive
disorder
characterized
by
low
mood,
loss
of
strength,
sadness,
insomnia,
inability
to
feel
pleasure.
In
outpatient
settings,
up
one-third
patients
with
depressive
symptoms
may
have
comorbidity.
Many
diseases
associated
symptoms.
Cardiovascular,
metabolic,
inflammatory,
oncological,
neurological
disorders
are
an
increased
risk
depression,
potentially
due
chronic
inflammation,
neurochemical
dysregulation,
emotional
social
issues.
drugs
can
cause
symptoms,
patient's
medical
history
should
include
assessment
use
such
drugs.
Primary
care
physicians
play
important
role
in
identifying
treating
depression.
It
recommended
perform
depression
screening
all
adult
female
primary
facilities.
There
general
recommendations
for
initial
treatment
mild
moderate
adults.
preference
be
given
psychotherapy
symptom
monitoring,
if
improvement
insufficient,
pharmacotherapy
used.
Psychotherapy,
or
combination
both
considered
Psychiatric
consultation
severe
urgently
any
patient
psychotic
suicidal
thoughts
behaviour.
Antidepressants
basic
therapy
Selective
serotonin
reuptake
inhibitors
first-line
treat
The Lancet Regional Health - Europe,
Journal Year:
2024,
Volume and Issue:
44, P. 101009 - 101009
Published: Aug. 23, 2024
Multiple
sclerosis
(MS)
is
an
immune-mediated
inflammatory
and
degenerative
disorder
of
the
central
nervous
system
(CNS)
with
heterogeneous
clinical
manifestations.
In
last
decade,
landscape
cerebrospinal
fluid
(CSF)
blood
biomarkers
as
potential
key
tools
for
MS
diagnosis,
prognosis
treatment
monitoring
has
evolved
considerably,
alongside
magnetic
resonance
imaging
(MRI).
CSF
analysis
not
only
to
provide
information
on
underlying
immunopathology
disease
exclude
differential
diagnoses,
but
also
predict
risk
future
relapses
disability
accrual,
guide
therapeutic
decisions
thus
improve
patient
outcomes.
This
Series
article
overviews
biological
framework
current
applicability
MS,
exploring
their
role
in
molecular
characterisation
disease.
We
discuss
recent
advances
field
neurochemistry
that
enabled
detection
brain-derived
proteins
blood,
opening
door
much
more
efficient
longitudinal
monitoring.
Furthermore,
we
identify
challenges
application
a
real-world
setting,
while
offering
recommendations
harnessing
full
paraclinical
management
personalise
treatment.
Autoimmunity Reviews,
Journal Year:
2025,
Volume and Issue:
24(6), P. 103784 - 103784
Published: March 3, 2025
Autoimmune
diseases
result
from
complex
interactions
between
genetic
and
environmental
factors.
Recent
advances
in
epigenetic
research
shed
light
on
the
intricate
regulatory
mechanisms
that
contribute
to
development
progression
of
such
conditions.
The
present
review
aims
explore
role
modifications,
including
DNA
methylation,
histone
non-coding
RNAs,
context
autoimmune
diseases.
We
discuss
current
understanding
alterations
associated
with
various
disorders,
their
impact
immune
cell
function,
potential
as
innovative
therapeutic
targets.
Additionally,
we
highlight
main
future
directions
field
epigenetics
autoimmunity.
Sclerosis,
Journal Year:
2025,
Volume and Issue:
3(1), P. 3 - 3
Published: Jan. 17, 2025
Background/Objectives:
Footfall
placement
variability
is
associated
with
falls
in
older
adults
and
neurological
diseases.
Thus,
the
study
of
dual-task
gait
impairment
middle-aged
to
older-aged
multiple
sclerosis
(MS)
clinically
relevant,
particularly
environments
that
mimic
obstacles
experienced
daily
ambulation.
Methods:
A
total
10
MS
(eight
female,
mean
±
SD
age
=
56
5
years),
12
healthy
(HOAs,
nine
63
4
young
(HYAs,
five
22
3)
were
asked
perform
cued
walking
(CW)
or
obstacle
(OW)
tasks
without
a
concurrent
backward
alphabet
recitation
task
(CWT,
OWT),
dual
tasks.
Gait
performance
attentional
demands
measured
using
hit
rate,
stride
velocity,
footfall
bias
variance,
prefrontal
cortex
(PFC)
oxygenated
hemoglobin
HbO
levels.
Results:
significant
condition-by-cohort
interaction
was
seen
variance
as
indicated
by
higher
vs.
single-task
conditions
HOAs,
comparison
HYAs
MS.
Further,
levels
PFC
OW
CW
MS,
compared
Conclusions:
The
decreased
accuracy
increased
attention
visual
cues
on
ground
observed
relative
HYAs,
may
provide
marker
for
fall
risk
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(3), P. 884 - 884
Published: Jan. 21, 2025
In
multiple
sclerosis
(MS),
there
is
significant
evidence
indicating
that
both
progression
independent
of
relapse
activity
(PIRA)
and
relapse-related
worsening
events
contribute
to
the
accumulation
progressive
disability
from
onset
disease
throughout
its
course.
Understanding
compartmentalized
pathophysiology
MS
would
enhance
comprehension
mechanisms,
overcoming
traditional
distinction
in
phenotypes.
Smoldering
thought
be
maintained
by
a
continuous
interaction
between
parenchymal
chronic
processes
neuroinflammation
neurodegeneration
intrathecal
compartment.
This
review
provides
comprehensive
up-to-date
overview
neuropathological
immunological
related
mechanisms
underlying
PIRA
phenomena
MS,
with
focus
on
studies
investigating
impact
currently
available
therapies
these
complex
mechanisms.
Brain Sciences,
Journal Year:
2025,
Volume and Issue:
15(2), P. 149 - 149
Published: Jan. 31, 2025
Multiple
sclerosis
(MS)
is
an
autoimmune
disease
classified
as
neurodegenerative
because
it
can
be
associated
with
the
more
or
less
progressive
development
of
neurological
symptoms
and
cognitive
deficits.
In
recent
years,
various
studies
have
started
to
investigate
eye
movements
in
relation
impairment
persons
MS
by
means
eye-tracking
equipment.
However,
high
heterogeneity
paradigms
used
different
studies,
well
methodologies
included,
makes
difficult
provide
a
complete
precise
picture
this
important
research
clinical
issue.
The
purpose
present
in-depth
scoping
review
was
map
existing
literature
field
determine
which
metrics
may
relevant
when
dealing
neurocognitive
profile
people
MS.
From
analyses
included
anti-saccade
latency
errors
were
most
frequently
proposed
metrics.
Correlation
between
these
measures
showed
significant
associations
them,
calling
for
deeper
investigation
promising
field.
results
strongly
suggest
that
tracking
play
crucial
role
practice
during
early
detection
disorders.
There
great
need
primary
addresses
full
complexity
its
phenotypes
disease-related
variables
from
multidisciplinary
perspective.
Future
should
clarify
whether
oculomotor
dysfunction
follows
precedes
Hereditas,
Journal Year:
2025,
Volume and Issue:
162(1)
Published: Feb. 14, 2025
Abstract
Background
and
purpose
Research
shows
that
people
with
multiple
sclerosis
(MS)
are
more
likely
to
experience
cardiovascular
complications.
However,
the
precise
mechanisms
underlying
this
association
remain
unclear.
This
study
investigated
causal
relationship
between
MS
coronary
heart
disease
(CHD)
using
Mendelian
randomization
(MR)
techniques
clarify
direct
effects
identify
relevant
target
genes.
Methods
We
conducted
various
methods,
including
two-sample
MR.
method,
reverse,
multivariable
MR
analyses,
examine
CHD.
These.
methodologies
effectively
mitigate
confounding
variables
neutralize
adverse
effects.
Additionally,
explored
involvement
of
social
factors
through
a
two-step
analysis.
The
research
team
performed
thorough
screening
differentially
expressed
genes
in
based
on
GEO
database,
identifying
potential
may
be
associated
genetic
risk
Enrichment
analyses
protein-protein
interaction
studies
were
used
elucidate
biological
functions
these
included
colocalization
analysis
summary
data-based
(SMR)
method
for
further
core
obtain
genes.Finally,
we
how
might
affect
health
by
conducting
phenome-wide
Results
Our
findings
revealed
predisposition
significantly
increases
CHD,
an
IVW-MR
yielding
odds
ratio
1.091
(95%
CI:
1.030,
1.155,
P
=
0.0029).
Mediation
frailty
mediated
20.2%
effect
CHD
(
0.026),
suggesting
is
critical
pathway
relationship.
low-density
lipoprotein
(LDL)
increased
developing
both
identified
3025
130
causally
linked
Protein-protein
network
77
interacting
genes,
such
as
SREBF1
involved
organelle
regulation
nucleic
acid
metabolism.
Colocalization
supported
presence
shared
variants
IL6R
posterior
probabilities
(PPH4)
90.2%
92.3%,
respectively.
Interestingly,
mendelian
gene
MS(bSMR=-0.174,PSMR
0.0218,
PHEIDI
0.2806,
topSNP:
rs12951376).
Further
did
not
find
significant
evidence
side
targeted
therapy
against
SREBF1.
Conclusion
provided
indicating
indivduals
face
higher
disease.
Furthermore,
maybe
which
would
contribute
drug
development.
Journal of Neurology,
Journal Year:
2025,
Volume and Issue:
272(3)
Published: Feb. 17, 2025
Abstract
The
role
of
B
cells
in
the
pathophysiology
multiple
sclerosis
(MS)
extends
beyond
antibody
synthesis,
also
involving
modulation
T
lymphocytes
and
myeloid
cells.
B-cell
activation
within
Central
Nervous
System
is
associated
with
release
various
antibodies,
cytokines,
chemokines,
measurable
biofluids,
thereby
serving
as
biomarkers
immune
processes
responsible
for
MS.
To
this
purpose,
a
biomarker-based
characterization
disease
through
combination
well-established
markers,
e.g.,
immunoglobulin
(Ig)
G
index,
IgG
oligoclonal
bands,
Ig
free
light
chains,
new
promising
namely
chemokine
(C–X–C
motif)
ligand
13,
activating
factor/A
proliferation-inducing
ligand,
might
represent
significant
improvement
management
people
Brain Sciences,
Journal Year:
2025,
Volume and Issue:
15(3), P. 248 - 248
Published: Feb. 26, 2025
Multiple
sclerosis
(MS)
is
an
autoimmune
disease
that
damages
the
myelin
sheath
around
central
nervous
system
axons,
leading
to
neurological
dysfunction.
Although
initial
damage
driven
by
inflammation,
hypoxia
has
been
reported
in
several
brain
regions
of
MS
patients,
but
significance
this
for
prognosis
and
treatment
remains
unclear.
Neuroinflammation
can
induce
hypoxia,
exacerbate
neuroinflammation,
forming
a
vicious
cycle.
Within
lesions,
demyelination
often
followed
remyelination,
which
may
restore
function.
However,
demyelinated
axons
are
vulnerable
damage,
leads
accumulation
permanent
dysfunction
typical
MS,
with
vulnerability
heightened
during
hypoxia.
Clinically
approved
therapies
immunomodulatory,
reduce
relapse
frequency/severity,
there
lack
pro-regenerative
example
promoting
remyelination.
All
tissues
have
protective
responses
be
relevant
especially
remyelinating
episodes.
When
oxygen
levels
reduced
brain,
constitutively
expressed
hypoxia-inducible
factors
(HIF)
stabilised,
upregulating
hundreds
genes,
including
neuroprotective
factors.
Furthermore,
astrocytes
upregulate
heparin-binding
epidermal
growth
factor
(EGF)-like
(HB-EGF)
early
stage
MS.
HB-EGF
promotes
mechanisms
induces
oligodendrocyte
neuron
differentiation
survival.
This
review
article
outlines
neuroinflammation
cycle
pathology
identifies
potential
therapeutic
targets
limit
neurodegeneration
and/or
promote
regeneration.
Both
HIF
signalling
pathways
endogenous
protection
CNS,
neuroprotection
remyelination
directly,
also
indirectly
modulating
immune
response
Promoting
such
could
effective
therapy
patients.