Alcoholism Clinical and Experimental Research,
Год журнала:
2022,
Номер
46(6), С. 994 - 1010
Опубликована: Апрель 22, 2022
Diminished
uptake
of
fluorodeoxyglucose
(FDG)
has
been
observed
in
patients
with
alcohol
use
disorder
(AUD)
but
little
statistical
contrast
the
regional
brain
deficits
undertaken.
This
study
examined
prefrontal
cortex
inter-regional
Brodmann
area
differences
to
delineate
patterns
associated
behavioral,
neurotransmitter,
and
general
toxicity
hypotheses
cerebral
involvement
AUD.We
obtained
data
from
FDG
positron
emission
tomography
(PET)
anatomical
magnetic
resonance
imaging
(MRI)
for
87
AUD
41
age-
sex-matched
healthy
volunteers.
Patients
were
dependent
had
negative
breathalyzer
tests
at
time
imaging.
They
assessed
Beck
Depression
Inventory,
Alcohol
Urge
Questionnaire,
Obsessive
Compulsive
Drinking
Scale,
Spielberger
State/Trait
Anxiety
Buss-Durkee
Hostility
Drinker
Inventory
Consequences
(DrInC).
PET
images
co-registered
MRI
both
voxel
×
mapping
stereotaxic
regions
interest
obtained.Compared
volunteers,
lower
relative
metabolic
rates
frontal,
temporal,
parietal
lobes,
localizable
most
prominently
dorsolateral
nearly
all
orbital
cortex,
superior
temporal
gyrus,
inferior
lobule.
In
contrast,
medial
orbitofrontal
anterior
cingulate
subcortical
structures
(thalamus,
cerebellum,
ventral
striatum,
dorsal
raphe
nucleus)
significantly
greater.
The
severity
alcohol-related
consequences
as
by
DrInC
scale
was
highly
metabolism
caudate,
prefrontal,
frontopolar,
anteroposterior
cortex.Despite
widespread
abnormalities,
decreases
marked
frontal
executive
areas,
consistent
diminished
impulse
control,
increases
prominent
striatum
a
suppressed
reward
system.
Nature Communications,
Год журнала:
2022,
Номер
13(1)
Опубликована: Март 4, 2022
Abstract
Heavy
alcohol
consumption
has
been
associated
with
brain
atrophy,
neuronal
loss,
and
poorer
white
matter
fiber
integrity.
However,
there
is
conflicting
evidence
on
whether
light-to-moderate
shows
similar
negative
associations
structure.
To
address
this,
we
examine
the
between
intake
structure
using
multimodal
imaging
data
from
36,678
generally
healthy
middle-aged
older
adults
UK
Biobank,
controlling
for
numerous
potential
confounds.
Consistent
prior
literature,
find
macrostructure
microstructure.
Specifically,
negatively
global
volume
measures,
regional
gray
volumes,
Here,
show
that
microstructure
are
already
apparent
in
individuals
consuming
an
average
of
only
one
to
two
daily
units,
become
stronger
as
increases.
Antioxidants,
Год журнала:
2022,
Номер
11(7), С. 1374 - 1374
Опубликована: Июль 15, 2022
Alcohol
use
disorder
(AUD)
is
a
highly
prevalent,
comorbid,
and
disabling
disorder.
The
underlying
mechanism
of
ethanol
neurotoxicity
the
involvement
oxidative
stress
still
not
fully
elucidated.
However,
metabolism
has
been
associated
with
increased
through
alcohol
dehydrogenase,
microsomal
oxidation
system,
catalase
metabolic
pathways.
We
searched
PubMed
genome-wide
association
studies
(GWAS)
catalog
databases
to
review
literature
systematically
summarized
findings
focusing
on
AUD
abstinence
in
relation
stress.
In
addition,
we
reviewed
ClinicalTrials.gov
resource
US
National
Library
Medicine
identify
all
ongoing
completed
clinical
trials
that
include
therapeutic
interventions
based
antioxidants.
retrieved
preclinical
show
impacts
genetics,
metabolism,
inflammation,
neurodegeneration.
Clinical Epigenetics,
Год журнала:
2025,
Номер
17(1)
Опубликована: Янв. 25, 2025
Abstract
Alcohol
consumption
is
an
important
risk
factor
for
multiple
diseases.
It
typically
assessed
via
self-report,
which
open
to
measurement
error
through
recall
bias.
Instead,
molecular
data
such
as
blood-based
DNA
methylation
(DNAm)
could
be
used
derive
a
more
objective
measure
of
alcohol
by
incorporating
information
from
cytosine-phosphate-guanine
(CpG)
sites
known
linked
the
trait.
Here,
we
explore
epigenetic
architecture
self-reported
weekly
units
in
Generation
Scotland
study.
We
first
create
score
(EpiScore)
using
elastic
net
penalized
linear
regression.
effect
pre-filtering
CpG
features
ahead
net,
well
differential
patterns
sex
and
consumed
last
week
relative
average
week.
The
final
EpiScore
was
trained
on
16,717
individuals
tested
four
external
cohorts:
Lothian
Birth
Cohorts
(LBC)
1921
1936,
Sister
Study,
Avon
Longitudinal
Study
Parents
Children
(total
N
across
studies
>
10,000).
maximum
Pearson
correlation
between
within
cohort
ranged
0.41
0.53.
In
LBC1936,
higher
levels
had
significant
associations
with
poorer
global
brain
imaging
metrics,
whereas
did
not.
Finally,
identified
two
novel
loci
Bayesian
regression
epigenome-wide
association
study
consumption.
Together,
these
findings
show
how
DNAm
can
objectively
characterize
that
associate
health,
unlike
estimates.
Oxford University Press eBooks,
Год журнала:
2025,
Номер
unknown, С. 23 - 34
Опубликована: Фев. 1, 2025
Abstract
Aging
is
a
critical
issue
for
families,
policymakers,
healthcare
providers,
and
society
at
large.
This
chapter
explores
the
biological,
environmental,
behavioural,
psychosocial
factors
that
influence
experience
of
aging
in
high-income
countries.
Age-related
decline,
emergence
chronic
disease,
social
isolation,
functional
changes
occur
context
urbanization,
population
shifts,
limitations
workforce
among
other
factors.
Responses
to
include
programmes
support
informal
carers,
implementation
integrated
models
healthcare,
mitigation
impact
health
well-being.
In
parallel
ideas
age-related
concepts
positive
emphasize
independence
minimize
disability
also
countries,
although
these
benefits
security
are
unequally
experienced
due
differential
exposure
environments
promote
well-being
or
illness.
Therapies
disease
policies
bolster
poorly
resourced
decrease
harmful
exposures
need
be
implemented
within
framework
equity.
Alcohol Clinical and Experimental Research,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 28, 2025
Abstract
Background
Chronic
heavy
alcohol
use
is
a
major
risk
factor
for
premature
aging
and
age‐related
diseases.
DNA
methylation
(DNAm)‐based
epigenetic
clocks
are
novel
tools
predicting
biological
age.
However,
the
newest
configurations,
causality‐enriched
clocks,
have
not
been
assessed
in
context
of
consumption
disorder
(AUD).
Methods
Epigenetic
was
evaluated
sample
615
individuals
(372
AUD
patients
243
healthy
controls)
by
applying
GrimAge
Version
1
(V1)
2
(V2)
alongside
three
(CausAge,
DamAge,
AdaptAge).
A
linear
model
controlling
diagnosis,
sex,
race,
BMI,
smoking
status,
five
blood
cell
types
leveraged
to
test
associations
between
alcohol‐related
metrics
age‐adjusted
clocks.
Results
V1
V2
maintained
significant
with
drinking
behavior
measures
within
total
both
young
(<40
years
old)
old
(≥40
subgroups.
Generally,
slightly
outperformed
V1,
while
none
demonstrated
AUD.
subgroup,
DamAge
had
association
number
drinks.
Across
age
subgroups,
liver
function
enzymes,
consistently
sustained
stronger
compared
V1.
Among
fourth‐generation
exhibited
gamma‐glutamyl
transferase
(GGT)
aspartate
aminotransferase
subgroup;
CausAge
displayed
GGT
sample.
Examining
clinical
biomarkers,
showed
improved
C‐reactive
protein
Conclusions
Overall,
we
observed
moderately
performance
majority
parameters
tested.
The
lacked
but
demonstrate
complexities
inspire
further
research
dynamics.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(7), С. 3272 - 3272
Опубликована: Апрель 1, 2025
Chronic
alcohol
consumption
leads
to
excessive
production
of
reactive
oxygen
species
(ROS),
driving
oxidative
stress
that
contributes
both
use
disorder
(AUD)
and
Alzheimer's
disease
(AD).
This
review
explores
how
ROS-mediated
mitochondrial
dysfunction
neuroinflammation
serve
as
shared
pathological
mechanisms
linking
these
conditions.
We
highlight
the
role
alcohol-induced
damage
in
exacerbating
neurodegeneration
compare
ROS-related
pathways
AUD
AD.
Finally,
we
discuss
emerging
therapeutic
strategies,
including
antioxidants
inflammasome
inhibitors,
target
mitigate
neurodegeneration.
Understanding
overlapping
may
provide
new
insights
for
preventing
treating
ROS-driven
neurodegenerative
disorders.
Cerebral Cortex,
Год журнала:
2021,
Номер
31(7), С. 3254 - 3265
Опубликована: Янв. 19, 2021
Abstract
Here
we
assessed
changes
in
subcortical
volumes
alcohol
use
disorder
(AUD).
A
simple
morphometry-based
classifier
(MC)
was
developed
to
identify
that
distinguished
32
healthy
controls
(HCs)
from
33
AUD
patients,
who
were
scanned
twice,
during
early
and
later
withdrawal,
assess
the
effect
of
abstinence
on
MC-features
(Discovery
cohort).
We
validated
novel
an
independent
Validation
cohort
(19
patients
20
HCs).
MC-accuracy
reached
80%
(Discovery)
72%
(Validation).
MC
features
included
hippocampus,
amygdala,
cerebellum,
putamen,
corpus
callosum,
brain
stem,
which
smaller
showed
stronger
age-related
decreases
than
HCs,
ventricles
cerebrospinal
fluid,
larger
older
participants.
The
volume
amygdala
a
positive
association
with
anxiety
negative
urgency
AUD.
Repeated
imaging
third
week
detoxification
revealed
slightly
consistent
partial
recovery
abstinence.
steeper
age-associated
volumetric
reductions
stress-
reward-related
regions
are
accelerated
aging,
whereas
amygdalar
associations
support
its
involvement
“dark
side
addiction”.
International Journal of Molecular Sciences,
Год журнала:
2022,
Номер
23(8), С. 4387 - 4387
Опубликована: Апрель 15, 2022
During
the
aging
process
our
body
becomes
less
well
equipped
to
deal
with
cellular
stress,
resulting
in
an
increase
unrepaired
damage.
This
causes
varying
degrees
of
impaired
functionality
and
increased
risk
mortality.
One
most
effective
anti-aging
strategies
involves
interventions
that
combine
simultaneous
glucometabolic
support
augmented
DNA
damage
protection/repair.
Thus,
it
seems
prudent
develop
therapeutic
target
this
combinatorial
approach.
Studies
have
shown
ADP-ribosylation
factor
(ARF)
GTPase
activating
protein
GIT2
(GIT2)
acts
as
a
keystone
process.
can
control
both
repair
glucose
metabolism.
Through
vivo
co-regulation
analyses
was
found
forms
close
coexpression-based
relationship
relaxin-3
receptor
(RXFP3).
Cellular
RXFP3
expression
is
directly
affected
by
oxidative
stress.
Overexpression
or
stimulation
receptor,
its
endogenous
ligand
relaxin
3
(RLN3),
regulate
response
processes.
Interestingly,
RLN3
insulin-like
peptide
has
been
multiple
disease
processes
linked
mechanisms,
e.g.,
anxiety,
depression,
memory
dysfunction,
appetite,
anti-apoptotic
mechanisms.
Here
we
discuss
molecular
mechanisms
underlying
various
roles
RXFP3/RLN3
signaling
age-related
disorders.