International Journal of Translational Medicine,
Год журнала:
2023,
Номер
3(1), С. 160 - 182
Опубликована: Март 8, 2023
Depression
and
obesity
are
highly
comorbid
with
one
another,
evidence
of
bidirectional
causal
links
between
each
disorder
a
shared
biological
basis.
Genetic
factors
play
major
role
in
influencing
both
the
occurrence
depression
obesity,
their
courses,
response
to
existing
treatments.
The
current
paper
is
scoping
review
studies
that
have
evaluated
contribution
specific
genetic
variants
comorbidity
depression.
Based
on
search
PubMed
EMBASE
databases,
28
were
included
this
review,
covering
54
candidate
genes.
Positive
associations
identified
for
14
loci
(AKR1C2,
APOA5,
COMT,
DAT1,
FTO,
KCNE1,
MAOA,
MC4R,
MCHR2,
NPY2R,
NR3C1,
Ob,
PCSK9,
TAL1).
Replicated
findings
across
two
or
more
independent
samples
observed
FTO
MC4R
Many
these
gene
products
represent
novel
molecular
targets
pharmacological
management
interact
other
not
pharmacologically
influenced
by
anti-obesity
antidepressant
medications.
implications
future
drug
development
discussed,
an
emphasis
recent
polygenic
architecture
precision-medicine
approach
conditions.
Nutrients,
Год журнала:
2023,
Номер
15(15), С. 3445 - 3445
Опубликована: Авг. 4, 2023
Obesity
is
a
metabolic
state
generated
by
the
expansion
of
adipose
tissue.
Adipose
tissue
depends
on
interplay
between
hyperplasia
and
hypertrophy,
mainly
regulated
complex
interaction
genetics
excess
energy
intake.
However,
genetic
regulation
yet
to
be
fully
understood.
can
divided
into
common
multifactorial/polygenic
obesity
monogenic
obesity,
non-syndromic
syndromic.
Several
genes
related
were
found
through
studies
models.
syndromic
characterized
additional
features
other
than
suggesting
more
global
role
mutant
syndrome
and,
thus,
an
peripheral
influence
development
hardly
studied
date
in
this
regard.
This
review
summarizes
present
knowledge
regarding
hypertrophy
adipocytes
obesity.
Additionally,
we
highlight
scarce
research
as
model
for
studying
adipocyte
focusing
Bardet–Biedl
(BBS).
BBS
involves
central
mechanisms,
with
molecular
mechanistic
alternation
hypertrophy.
Thus,
argue
that
using
models,
such
BBS,
further
advance
our
Medicine,
Год журнала:
2025,
Номер
104(19), С. e42378 - e42378
Опубликована: Май 9, 2025
Obesity
is
a
multifactorial
disease,
commonly
observed
both
worldwide
and
in
our
country,
triggered
by
environmental
genetic
factors,
adversely
affecting
all
physiological
functions
of
the
body,
leading
to
an
increase
body
fat
mass.
Although
various
variants
associated
with
susceptibility
obesity
have
been
identified
genomic
studies,
these
explain
only
small
portion
basis
obesity.
This
case-control
study
investigates,
for
first
time
Turkish
population,
relationship
between
CYP1B1
gene
rs1056827
rs1056836
polymorphisms
patients
undergoing
surgical
intervention
(bariatric
surgery).
Genotyping
was
performed
using
Real-Time
PCR
63
female
29
male
who
underwent
bariatric
surgery
40
51
nonobese
individuals.
In
study,
genotype
distributions
polymorphism
were
found
be
51.1%
CC,
40.2%
CG,
8.7%
GG
case
group
46.2%
47.3%
6.6%
control
group.
The
frequency
C
allele
71.2%,
G
28.8%
group,
while
70.3%,
29.7%
For
polymorphism,
10.8%
GG,
35.9%
GT,
53.3%
TT
7.7%
49.4%
42.9%
28.8%,
T
71.2%
whereas
32.4%,
67.6%
No
significant
difference
groups
terms
anthropometric
measurements
biochemical
parameter
values
gene.
Our
valuable
as
it
investigate
association
CYP1B1*2
(rs1056827)
CYP1B1*3
(rs1056836)
obesity,
determined
that
there
no
investigated
Frontiers in Endocrinology,
Год журнала:
2023,
Номер
14
Опубликована: Авг. 9, 2023
Background
The
relationships
of
the
rs17782313
polymorphism
near
melanocortin
4
receptor
gene
(MC4R)
and
rs8192678
in
peroxisome
proliferator-activated
gamma
coactivator
1
alpha
(PGC1α)
with
metabolic
abnormalities
have
been
explored
many
populations
around
world,
but
findings
were
not
all
consistent
sometimes
even
a
bit
contradictory.
Methods
Electronic
databases
including
Medline,
Scopus,
Embase,
Web
Science,
CNKI
Google
Scholar
checked
for
studies
that
met
inclusion
criteria.
Data
carefully
extracted
from
eligible
studies.
Standardized
mean
differences
(SMDs)
calculated
by
using
random-effects
model
to
examine
indexes
obesity,
glucometabolic
disorder
dyslipidemia
between
genotypes
polymorphisms.
Cochran’s
Q-statistic
test
Begg’s
employed
identify
heterogeneity
among
publication
bias,
respectively.
Results
Fifty
(58,716
subjects)
51
(18,660
respectively
included
pooled
meta-analyses
C-allele
carriers
had
higher
average
level
body
mass
index
(SMD
=
0.21
kg/m
2
,
95%
confidence
interval
[95%
CI]
0.12
0.29
p
<
0.001),
waist
circumference
0.14
cm,
CI
0.06
0.23
0.001)
blood
glucose
0.09
mg/dL,
0.02
0.16
0.01)
than
TT
homozygotes.
Regarding
polymorphism,
no
significant
associations
detected.
However,
correlations
multiple
observed
subgroup
analyses
stratified
sex,
age,
ethnicity
health
status.
Conclusion
meta-analysis
demonstrates
C
allele
MC4R
confers
risk
obesity
hyperglycemia,
PGC1α
is
weakly
correlated
disorder.
These
may
partly
explain
these
variants
diabetes
as
well
cardiovascular
disease.
Systematic
review
registration
https://www.crd.york.ac.uk/prospero/
identifier
CRD42022373543.
Molecular and Cellular Endocrinology,
Год журнала:
2023,
Номер
578, С. 112072 - 112072
Опубликована: Сен. 21, 2023
The
lining
of
our
intestinal
surface
contains
an
array
hormone-producing
cells
that
are
collectively
bodies'
largest
endocrine
cell
reservoir.
These
"enteroendocrine"
(EE)
reside
amongst
the
billions
absorptive
epithelial
and
other
types
line
gastrointestinal
tract
can
sense
respond
to
ever-changing
internal
environment
in
gut.
EE
release
important
signalling
molecules
act
as
hormones,
including
glucagon-like
peptide
(GLP-1)
YY
(PYY)
which
co-secreted
from
L
cells.
While
much
is
known
about
effects
these
hormones
on
metabolism,
insulin
secretion
food
intake,
less
understood
their
human
tissue.
In
this
study
we
assess
whether
GLP-1
PYY
differs
across
small
large
tissue
locations
within
tract,
and/or
by
sex,
body
weight
age
individual.
We
identify
both
greater
more
distal
regions
colon,
but
not
different
between
sexes.
observe
a
negative
correlation
BMI
small,
large,
intestine.
Increased
aging
correlates
with
declining
When
data
for
intestine
isolated
region,
relationship
remains
significant
ascending
descending
colon
PYY.
This
first
demonstration
site-specific
differences
occur
gut,
do
relationships
mass.
Genes,
Год журнала:
2023,
Номер
14(11), С. 1996 - 1996
Опубликована: Окт. 25, 2023
The
global
rise
in
obesity
is
attributed
to
genetic
predisposition
interaction
with
an
obesogenic
environment.
Melanocortin
4
receptor
(MC4R)
rs17782313
polymorphism
has
been
linked
common
varying
influence
across
different
populations.
MC4R
a
crucial
player
the
leptin
proopiomelanocortin
pathway
that
regulates
weight
hemostasis.
We
aimed
study
and
its
eating
behaviors
on
Israeli
population.
Adults’
(n
=
5785,
>18
y)
genotype
anthropometric
demographic
data
were
analyzed
using
logistic
regression
models
adjusting
for
age,
sex,
T1DM,
T2DM.
significantly
predisposes
elevated
risk
under
recessive
additive
(OR
1.38,
95%
CI:
1.1–1.72,
p
0.005
OR
1.1,
1.01–1.2,
0.03,
respectively)
adjusted
confounders
(age,
T2DM).
Stratification
by
sex
demonstrated
carrying
associated
model
among
females
only
1.41,
1.09–1.82,
0.01),
average
of
0.85
BMI
increment
compared
wild
type
one
allele
carriers.
interacted
several
enhance
obesity.
Our
findings
demonstrate
homozygous
female
carriers
are
predisposed
amplified
behaviors.
Frontiers in Nutrition,
Год журнала:
2024,
Номер
11
Опубликована: Май 28, 2024
Introduction
Appetitive
traits
are
influenced
by
the
interplay
between
genetic
and
environmental
factors.
This
study
aimed
to
explore
relationship
gene
polymorphisms
involved
in
regulation
of
energy
balance
food
reward
appetitive
young
Mexican
subjects.
Methods
cross-sectional
118
university
freshman
undergraduates
who
completed
Adult
Eating
Behaviour
Questionnaire
for
Spanish
speakers
(AEBQ-Esp)
assess
their
traits.
A
real-time
PCR
system
was
employed
determine
(
LEP
rs7799039,
MC4R
rs17782313,
FTO
rs9939609,
GHRL
rs696217),
DRD2/ANKK1
Taq1A
rs1800497
COMT
rs4680).
Results
The
mean
age
participants
20.14
±
3.95
years,
71.2%
were
women
BMI
23.52
4.05
kg/m
2
.
Met
allele
carriers
presented
a
significantly
higher
“Emotional
overeating”
score
than
Val
(2.63
0.70
vs.
2.23
0.70,
p
=
0.028).
CC
+
CT
genotype
correlated
positively
with
(Phi
0.308,
0.01).
MetMet+MetVal
r
0.257,
0.028;
Phi
0.249,
0.033).
protective
TT
undereating”
0.298,
0.012).
Carriers
risk
(OR
2.4,
95%
CI
1.3–4.8,
0.034).
3.4,
1.1–10.3,
0.033),
associated
ValVal
carriers.
1.8,
1.1–9.1,
0.014).
Discussion
found
genotypes
Met/Met+Met/Val
overeating.”
These
factors
may
increase
weight
gain
enhancing
hedonic
consumption
reducing
satiety
control.
Future
studies
should
focus
on
replication
ethnically
diverse
adults
life
stages
weight.
will
help
tailor
personalized
nutrigenetic
strategies
counteract
disordered
eating
patterns
leading
obesity
co-morbidities.
Nutrition Reviews,
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 14, 2024
Abstract
Context
The
melanocortin-4
receptor
gene
(MC4R)
is
associated
with
a
higher
risk
of
obesity
by
the
presence
C
allele
in
rs17782313,
but
mechanisms
are
not
clear.
Objective
present
systematic
review
and
meta-analysis
aimed
to
explore
association
between
different
genotypes
MC4R
rs17782313
energy
intake
appetite.
Data
Sources
A
literature
search
was
conducted
up
June
2023
PubMed,
Scopus,
Web
Science,
Cochrane
Collaboration
databases,
following
PRISMA
guidelines.
Extraction
Inclusion
criteria
were
studies
humans
measuring
intake,
appetite,
or
satiety
all
ages
physiological
conditions.
Studies
dealing
solely
body
mass
index
excluded.
Twenty-one
articles
representing
48
560
participants
included
meta-analysis.
Analysis
According
NHLBI
(National
Heart,
Lung,
Blood
Institute)
quality-assessment
criteria,
case-control
6
out
17
cohort
cross-sectional
classified
as
“good,”
while
rest
scored
“fair.”
Odds
ratios
(ORs)
95%
confidence
intervals
(CIs)
calculated
(CT+CC)
vs
TT
dominant
model,
both
random-effects
fixed-effects
models
used.
statistically
significant
increased
appetite
found
(OR
=
1.25;
CI:
1.01–1.49;
P
.038)
using
model
proved
nonsignificant.
However,
no
found.
None
variables
considered
(sample
size,
year
publication,
sex,
age
group,
type
population,
origin,
quality)
identified
effect
modifiers,
publication
biases
after
subgroup
meta-regression
analyses.
Conclusion
To
our
knowledge,
this
first
that
has
analyzed
Identifying
people
genetically
predisposed
may
be
great
interest,
only
prevent
younger
populations
also
avoid
malnutrition
elderly
persons.
This
paper
part
Nutrition
Reviews
Special
Collection
on
Precision
.
Systematic
Review
Registration
PROSPERO
registration
no.
CRD42023417916.