Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Sept. 15, 2023
Abstract
Child
maltreatment
(CM)
leads
to
adverse
outcomes
in
later
life.
We
describe
the
epigenome-wide
analyses
and
meta-analysis
results
of
three
original
cohorts
consisting
judicially
or
socially
certified
CM
cases
controls
gain
further
insight
into
epigenetic
signatures
engraved
maltreated
children.
also
show
associations
with
biological
indicators
(endophenotypes)
each
cohort
that
represent
features
history,
thus
providing
confidence
identified
methylations.
Four
methylations
ATE1
,
CHST11
SERPINB9P1
FOXP1
associate
meta-analysis,
addition
several
genome-wide
level
significant
cohort.
a
gene
related
neurodevelopmental
disorders,
is
particular
interest,
as
its
methylation
correlates
atypical
brain
structures
representing
children
contributes
accuracy
risk
score
predict
CM.
These
suggest
severe
experiences
may
contribute
neurodevelopmental-like
traumatic
symptoms
via
alterations.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 16, 2024
Abstract
The
genetic
makeup
of
parents
can
directly
or
indirectly
affect
their
offspring
phenome
through
transmission
via
the
environment
that
is
influenced
by
parental
heritable
traits.
Our
understanding
mechanisms
which
indirect
effects
operate
limited.
Here,
we
hypothesize
one
mechanism
methylome.
To
test
this
hypothesis,
polygenic
scores
(PGSs)
for
schizophrenia,
smoking
initiation,
educational
attainment
(EA),
social
deprivation,
body
mass
index
(BMI),
and
height
were
analyzed
in
a
cohort
1,528
(51.5%
boys,
mean
[
SD
]
age
=
10
[2.8]
years).
We
modelled
parent
PGSs
on
buccal-DNA
methylation,
accounting
own
PGS
offspring,
found
significant
associations
between
EA,
BMI,
height,
buccal
methylation
sites,
comprising
16,
2,
1,
6
respectively
(alpha
2.7
×
−5
).
More
DNA
sites
associated
with
maternal
than
paternal
PGSs,
possibly
reflecting
pre-
periconceptional
stronger
involvement
shaping
offspring’s
during
early
childhood.
Trauma und Gewalt,
Journal Year:
2024,
Volume and Issue:
18(2), P. 170 - 175
Published: April 23, 2024
Frühe
biografische
Traumatisierungen
in
Form
von
Missbrauch
und
Vernachlässigung
stellen
allgemeine
Risikofaktoren
für
eine
große
Bandbreite
psychopathologischer
Phänomene
psychischer
Störungen
dar.
In
der
klinischen
Praxis
gibt
es
immer
wieder
Einzelfälle
mit
einer
hohen
intraindividuellen
Variabilität
Psychopathologie
über
die
Lebensspanne.
Mit
hier
präsentierten
Krankengeschichte
eines
Anfang
50-jährigen
Mannes
wird
illustriert,
dass
schwerer
körperlicher
Missbrauch,
den
Patient
bis
zu
seinem
16.
Lebensjahr
durch
seinen
Stiefvater
erlitten
hat,
Aggressivität
bzw.
Delinquenz,
Substanzabhängigkeit,
einem
ängstlich-depressiven
Syndrom
chronischen
Schmerzen
assoziiert
sein
kann.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 10, 2024
Abstract
Aims
It
is
unclear
whether
DNA
methylation
underlies
the
associations
of
childhood
maltreatment
(CM)
with
non-suicidal
self-injury
(NSSI)
in
adolescents.
We
aim
to
explore
mediating
effect
specific
sites’
levels
on
CM
and
its
subtypes
NSSI,
following
investigation
association
between
NSSI.
Methods
A
nested
case-control
study
was
conducted
examine
155
adolescents
aged
12–14
years
who
had
NSSI
201
controls.
were
evaluated
using
Childhood
Trauma
Questionnaire.
The
850k
chip
used
discover
differences
whole
genome
peripheral
blood
10
cases
Pyrosequencing
employed
detect
differential
sites
among
population,
which
selected
based
bioinformatics
analysis.
Results
After
controlling
for
potential
confounders,
subtypes,
cg04622888cg05037505
all
significantly
associated
level
mediated
emotional
abuse
(proportion
estimates:
0.09;
95%
CI:
0.06–0.14),
neglect
(0.08;
95%CI:
0.05–0.13),
or
physical
(0.18;
0.08–0.31)
(0.14;
0.06–0.25)
Conclusions
independently
early
adolescents,
they
partially
abuse,
neglect,
Targeted
interventions
should
focus
individuals
have
experienced
exhibit
high
cg05037505.
Endocrine
and
nervous
systems
reciprocally
interact
to
manage
physiological
individual
functions
homeostasis.
The
system
modulates
hormone
release
through
the
hypothalamus,
main
cerebrally
specialized
structure
of
neuroendocrine
system.
Indeed,
it
is
involved
in
various
metabolic
processes,
administering
neuropeptide
at
different
levels.
This
complex
activity
affected
by
neurons
cerebral
areas,
environmental
factors,
peripheral
organs,
mediators
feedback
mechanisms.
Therefore,
pathways
have
a
key
role
homeostasis
control,
their
abnormalities
been
associated
with
development
Metabolic
Syndrome
(MetS)
children.
impaired
functioning
genes,
hormones,
neuropeptides
several
processes
has
related
an
increased
risk
dyslipidaemia,
visceral
obesity,
insulin
resistance,
type
2
diabetes
mellitus,
hypertension.
review
examines
effects
on
MetS
children,
identifying
underlying
conditions
pathway
disruption.
Neuroendocrine
should
be
considered
pathophysiology
MetS,
and,
when
genetic
or
epigenetic
mutations
"hot"
occur,
they
could
studied
for
new
potential
target
therapies
severe
drug-resistant
paediatric
forms
MetS.
Journal of Medical Ethics,
Journal Year:
2023,
Volume and Issue:
50(4), P. 272 - 277
Published: June 2, 2023
Ethical
debates
around
genetic
enhancement
tend
to
include
an
argument
that
the
technology
will
eventually
be
fairly
accessible
once
available.
That
we
can
distribute
has
become
a
moral
defence
of
enhancement.
Two
distribution
solutions
are
argued
for,
first
being
equal
distribution.
Equality
access
is
generally
believed
fairest
and
most
just
method
Second,
equitable
distribution:
providing
enhancements
reduce
social
inequalities.
In
this
paper,
I
make
two
claims.
argue
very
assumption
distributed
problematic
when
considering
our
understanding
gene-environment
interactions,
for
example,
epigenetics.
then
arguments
permissible
because
intended
benefits
as
misinformed.
My
claim
rests
on
assertion
do
not
enhance
traits
in
vacuum;
genes
dependent
conducive
environments
expression.
If
society
cannot
guarantee
fair
environments,
any
benefit
conferred
from
genetically
enhanced
undermined.
Thus,
therefore
morally
permissible,
mistaken.
Metabolites,
Journal Year:
2023,
Volume and Issue:
13(7), P. 810 - 810
Published: June 29, 2023
The
endocrine
and
nervous
systems
reciprocally
interact
to
manage
physiological
individual
functions
homeostasis.
system
modulates
hormone
release
through
the
hypothalamus,
main
cerebrally
specialized
structure
of
neuroendocrine
system.
hypothalamus
is
involved
in
various
metabolic
processes,
administering
neuropeptide
at
different
levels.
This
complex
activity
affected
by
neurons
cerebral
areas,
environmental
factors,
peripheral
organs,
mediators
feedback
mechanisms.
Therefore,
pathways
play
a
key
role
homeostasis
control,
their
abnormalities
are
associated
with
development
syndrome
(MetS)
children.
impaired
functioning
genes,
hormones,
neuropeptides
several
processes
related
an
increased
risk
dyslipidaemia,
visceral
obesity,
insulin
resistance,
type
2
diabetes
mellitus,
hypertension.
review
examines
effects
on
MetS
children,
identifying
underlying
conditions
pathway
disruption.
Neuroendocrine
should
be
considered
pathophysiology
MetS,
and,
when
genetic
or
epigenetic
mutations
“hot”
occur,
they
could
studied
for
new
potential
target
therapies
severe
drug-resistant
paediatric
forms
MetS.
Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Sept. 15, 2023
Abstract
Child
maltreatment
(CM)
leads
to
adverse
outcomes
in
later
life.
We
describe
the
epigenome-wide
analyses
and
meta-analysis
results
of
three
original
cohorts
consisting
judicially
or
socially
certified
CM
cases
controls
gain
further
insight
into
epigenetic
signatures
engraved
maltreated
children.
also
show
associations
with
biological
indicators
(endophenotypes)
each
cohort
that
represent
features
history,
thus
providing
confidence
identified
methylations.
Four
methylations
ATE1
,
CHST11
SERPINB9P1
FOXP1
associate
meta-analysis,
addition
several
genome-wide
level
significant
cohort.
a
gene
related
neurodevelopmental
disorders,
is
particular
interest,
as
its
methylation
correlates
atypical
brain
structures
representing
children
contributes
accuracy
risk
score
predict
CM.
These
suggest
severe
experiences
may
contribute
neurodevelopmental-like
traumatic
symptoms
via
alterations.