Epileptic Disorders,
Journal Year:
2023,
Volume and Issue:
25(5), P. 649 - 669
Published: June 30, 2023
The
pharmacological
treatment
of
epilepsy
entails
several
critical
decisions
that
need
to
be
based
on
an
individual
careful
risk-benefit
analysis.
These
include
when
initiate
and
with
which
antiseizure
medication
(ASM).
With
more
than
25
ASMs
the
market,
physicians
have
opportunities
tailor
patients´
needs.
ASM
selection
is
primarily
patient's
type
spectrum
efficacy,
but
other
factors
must
considered.
age,
sex,
comorbidities,
concomitant
medications
mention
most
important.
Individual
susceptibility
adverse
drug
effects,
ease
use,
costs,
personal
preferences
should
also
taken
into
account.
Once
has
been
selected,
next
step
decide
target
maintenance
dose
a
titration
scheme
reach
this
dose.
When
clinical
circumstances
permit,
slow
generally
preferred
since
it
associated
improved
tolerability.
adjusted
response
aiming
at
lowest
effective
Therapeutic
monitoring
can
value
in
efforts
establish
optimal
If
first
monotherapy
fails
control
seizures
without
significant
will
gradually
switch
alternative
monotherapy,
or
sometimes
add
another
ASM.
add-on
considered,
combining
different
modes
action
usually
recommended.
Misdiagnosis
epilepsy,
non-adherence
suboptimal
dosing
are
frequent
causes
failure
excluded
before
patient
regarded
as
drug-resistant.
Other
modalities,
including
surgery,
neuromodulation,
dietary
therapies,
considered
for
truly
drug-resistant
patients.
After
some
years
seizure
freedom,
question
withdrawal
often
arises.
Although
successful
many,
risks
decision
needs
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(7), P. 6050 - 6050
Published: March 23, 2023
The
anti-epileptic
drug
lamotrigine
(LTG)
has
been
widely
used
to
treat
various
neurological
disorders,
including
epilepsy
and
bipolar
disorder.
However,
its
precise
mechanism
of
action
in
the
central
nervous
system
(CNS)
still
needs
be
determined.
Recent
studies
have
highlighted
involvement
LTG
modulating
activity
voltage-gated
ion
channels,
particularly
those
related
inhibition
neuronal
excitability.
Additionally,
found
neuroprotective
effects,
potentially
through
glutamate
release
enhancement
GABAergic
neurotransmission.
LTG's
unique
compared
other
drugs
led
investigation
use
treating
CNS
such
as
neuropathic
pain,
PTSD,
major
depressive
Furthermore,
combined
with
mood
stabilizers,
which
may
enhance
therapeutic
effects.
In
conclusion,
potential
modulate
multiple
neurotransmitters
channels
makes
it
a
promising
for
disorders.
As
our
understanding
continues
evolve,
new
indications
will
also
explored.
Epileptic Disorders,
Journal Year:
2023,
Volume and Issue:
25(4), P. 454 - 471
Published: May 11, 2023
Abstract
Antiseizure
medications
(ASMs)
are
the
cornerstone
of
treatment
for
patients
with
epilepsy.
Several
new
ASMs
have
recently
been
introduced
to
market,
making
it
possible
better
tailor
epilepsy,
as
well
other
indications
(psychiatry
and
pain
disorders).
For
this
group
drugs
there
numerous
pharmacological
challenges,
updated
knowledge
on
their
pharmacodynamic
pharmacokinetic
properties
is,
therefore,
crucial
an
optimal
outcome.
This
review
focuses
educational
approaches
following
learning
outcomes
described
by
International
League
Against
Epilepsy
(ILAE):
To
demonstrate
pharmacokinetics
pharmacodynamics,
drug
interactions
concomitant
medications,
appropriate
monitoring
ASM
serum
levels
(therapeutic
monitoring,
TDM).
Basic
principles
in
pharmacology,
variability,
clinically
relevant
manage
discussed.
Furthermore,
recent
improvements
analytical
technology
sampling
described.
Future
directions
point
combined
implementation
TDM
genetic
panels
proper
diagnosis,
pharmacogenetic
tests
where
relevant,
use
biochemical
markers
that
will
all
contribute
personalized
treatment.
These
outcome
various
patient
groups.
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: May 12, 2023
Developmental
and
epileptic
encephalopathies
are
rare,
treatment-resistant
epilepsies
with
high
seizure
burden
non-seizure
comorbidities.
The
antiseizure
medication
(ASM)
fenfluramine
is
an
effective
treatment
for
reducing
frequency,
ameliorating
comorbidities,
potentially
risk
of
sudden
unexpected
death
in
epilepsy
(SUDEP)
patients
Dravet
syndrome
Lennox-Gastaut
syndrome,
among
other
rare
epilepsies.
Fenfluramine
has
a
unique
mechanism
action
(MOA)
ASMs.
Its
primary
MOA
currently
described
as
dual-action
sigma-1
receptor
serotonergic
activity;
however,
mechanisms
may
be
involved.
Here,
we
conduct
extensive
review
the
literature
to
identify
all
previously
fenfluramine.
We
also
consider
how
these
play
role
reports
clinical
benefit
outcomes,
including
SUDEP
everyday
executive
function.
Our
highlights
importance
serotonin
maintaining
balance
between
excitatory
(glutamatergic)
inhibitory
(γ-aminobutyric
acid
[GABA]-ergic)
neural
networks,
suggests
that
represent
pharmacological
MOAs
seizures,
SUDEP.
describe
ancillary
roles
GABA
neurotransmission,
noradrenergic
endocrine
system
(especially
such
progesterone
derivatives
neuroactive
steroids).
Dopaminergic
activity
underlies
appetite
reduction,
common
side
effect
treatment,
but
any
involvement
reduction
remains
speculative.
Further
research
underway
evaluate
promising
new
biological
pathways
A
better
understanding
comorbidities
allow
rational
drug
design
and/or
improved
decision-making
when
prescribing
multi-ASM
regimens.
Epilepsia,
Journal Year:
2024,
Volume and Issue:
65(3), P. 533 - 541
Published: Jan. 27, 2024
Abstract
A
variety
of
terms,
such
as
“antiepileptic,”
“anticonvulsant,”
and
“antiseizure”
have
been
historically
applied
to
medications
for
the
treatment
seizure
disorders.
Terminology
is
important
because
using
terms
that
do
not
accurately
reflect
action
specific
treatments
may
result
in
a
misunderstanding
their
effects
inappropriate
use.
The
present
International
League
Against
Epilepsy
(ILAE)
position
paper
used
Delphi
approach
develop
recommendations
on
English‐language
terminology
applicable
pharmacological
agents
currently
approved
treating
There
was
consensus
these
should
be
collectively
named
“antiseizure
medications”.
This
term
reflects
primarily
symptomatic
effect
against
seizures
reduces
possibility
health
care
practitioners,
patients,
or
caregivers
having
undue
expectations
an
incorrect
understanding
real
medications.
describe
does
exclude
beneficial
course
disease
comorbidities
from
downstream
seizures,
whenever
can
explained
solely
by
suppression
activity.
It
acknowledged
other
treatments,
mostly
under
development,
exert
direct
favorable
actions
underlying
its
progression,
“antiepileptogenic”
“disease‐modifying”
effects.
more‐refined
precisely
needs
developed.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(1), P. 119 - 119
Published: Jan. 13, 2024
The
infection
of
the
central
nervous
system
(CNS)
with
neurotropic
viruses
induces
neuroinflammation
and
is
associated
development
neuroinflammatory
neurodegenerative
diseases,
including
multiple
sclerosis
epilepsy.
activation
innate
adaptive
immune
response,
microglial,
macrophages,
T
B
cells,
while
required
for
efficient
viral
control
within
CNS,
also
neuropathology.
Under
healthy
conditions,
resident
microglia
play
a
pivotal
role
in
maintaining
CNS
homeostasis.
However,
during
pathological
events,
such
as
infection,
become
reactive,
cells
from
periphery
infiltrate
into
brain,
disrupting
homeostasis
contributing
to
disease
development.
Theiler's
murine
encephalomyelitis
virus
(TMEV),
picornavirus,
used
two
distinct
mouse
models:
TMEV-induced
demyelination
(TMEV-IDD)
seizures,
representing
models
epilepsy,
respectively.
These
have
contributed
substantially
our
understanding
pathophysiology
MS
seizures/epilepsy
following
serving
critical
tools
identifying
pharmacological
targetable
pathways
modulate
This
review
aims
discuss
host-pathogen
interaction
picornavirus
shed
light
on
current
multifaceted
roles
played
by
macrophages
context
these
complexes
viral-induced
disease.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Jan. 18, 2024
Abstract
Epilepsy
is
a
prevalent
disorder
involving
neuronal
network
hyperexcitability,
yet
existing
therapeutic
strategies
often
fail
to
provide
optimal
patient
outcomes.
Chemogenetic
approaches,
where
exogenous
receptors
are
expressed
in
defined
brain
areas
and
specifically
activated
by
selective
agonists,
appealing
methods
constrain
overactive
activity.
We
developed
BARNI
(Bradanicline-
Acetylcholine-activated
Receptor
for
Neuronal
Inhibition),
an
engineered
channel
comprised
of
the
α7
nicotinic
acetylcholine
receptor
ligand-binding
domain
coupled
α1
glycine
anion
pore
domain.
Here
we
demonstrate
that
activation
clinical
stage
receptor-selective
agonist
bradanicline
effectively
suppressed
targeted
activity,
controlled
both
acute
chronic
seizures
male
mice.
Our
results
evidence
use
inhibitory
acetylcholine-based
activatable
endogenous
agonists
as
potential
approach
treating
epilepsy.
The Lancet Regional Health - Europe,
Journal Year:
2024,
Volume and Issue:
38, P. 100849 - 100849
Published: Feb. 8, 2024
The
short-
and
long-term
consequences
of
restricted
fetal
growth
cause
considerable
concern,
how
prenatal
exposure
to
different
antiseizure
medications
(ASMs)
affects
remains
uncertain.
This
was
a
population-based
cohort
study
liveborn
singleton
children
born
in
Denmark,
Finland,
Iceland,
Norway,
Sweden
from
1996
2017.
Prenatal
defined
as
maternal
filling
prescriptions
for
ASM
during
pregnancy
registered
national
prescription
registries
primary
outcomes
were
adjusted
odds
ratios
(aORs)
microcephaly
or
being
small
gestational
age.
We
identified
4,494,918
(males:
51.3%,
2,306,991/4,494,918),
including
38,714
(0.9%)
mothers
with
epilepsy.
In
the
overall
population,
monotherapy
carbamazepine
(aOR:
1.25
(95%
CI:
1.12–1.40)),
pregabalin
1.16
1.02–1.31)),
oxcarbazepine
1.48
1.28–1.71)),
clonazepam
1.27
1.10–1.48)),
topiramate
1.18–1.85))
associated
risk
age,
1.43
1.17–1.75)).
epilepsy,
1.11–1.47)),
1.42
1.18–1.70)),
1.40
1.03–1.89)),
1.86
1.36–2.54))
age;
carbamazepine,
1.51
1.17–1.95)).
No
associations
age
after
lamotrigine,
valproate,
gabapentin,
levetiracetam,
phenobarbital,
acetazolamide,
phenytoin,
clobazam,
primidone,
zonisamide,
vigabatrin,
ethosuximide
lacosamide,
but
except
numbers
exposed
small.
oxcarbazepine,
clonazepam,
increased
both
population
women
epilepsy
suggesting
that
these
drugs
is
restriction.
NordForsk
Nordic
Program
on
Health
Welfare
(83539),
Independent
Research
Fund
Denmark
(1133-00026B),
Danish
Epilepsy
Association,
Central
Region,
Novo
Nordisk
Foundation
(NNF16OC0019126
NNF22OC0075033),
Lundbeck
(R400-2022-1205).
CNS Drugs,
Journal Year:
2024,
Volume and Issue:
38(9), P. 733 - 742
Published: Aug. 3, 2024
Cenobamate
(CNB)
is
a
new
antiseizure
medication
(ASM)
to
treat
drug-resistant,
focal-onset
seizures.
Data
on
its
use
in
early
therapy
lines
are
not
yet
available,
and
clinicians
frequently
consider
CNB
be
later
ASM
drug
choice.
We
investigated
the
efficacy
safety
of
as
an
adjunctive
treatment
The
study
population
were
patients
with
seizures
who
initiated
after
they
did
respond
two
or
three
lifetime
ASMs,
including
all
prior
concomitant
ASMs.
These
matched
(1:2)
by
sex,
age,
seizure
frequency
controls
any
other
than
CNB.
All
participants
participated
Mainz
Epilepsy
Registry.
evaluated
retention
rate
12
months
each
control
group.
In
addition,
freedom
response
(reduction
≥
50%
from
baseline)
estimated.
included
231
aged
44.4
±
15.8
years.
Of
these,
33.3%
(n
=
77)
CNB,
19.0%
44)
valproate
(VPA),
17.3%
40)
lacosamide
(LCS),
16.4%
38)
levetiracetam
(LEV),
13.9%
32)
topiramate
(TPM).
highest
since
beginning
was
observed
(92.0%),
compared
LCS
(80.0%),
LEV
(73.3%),
VPA
(68.2%),
TPM
(62.5%)
(p
<
0.05).
Seizure
also
best
(19.5%
71.4%,
respectively)
ASMs
(8.3%
52.5%,
respectively;
p
No
significant
differences
adverse
events
between
observed.
Our
provides
evidence
that
effective
good
profile
This
data
should
support
medical
decision
making
management
refractory
epilepsy.
NCT05267405.
Neurotherapeutics,
Journal Year:
2025,
Volume and Issue:
unknown, P. e00524 - e00524
Published: Jan. 1, 2025
Electroencephalography
(EEG)
is
invaluable
in
the
management
of
acute
neurological
emergencies.
Characteristic
EEG
changes
have
been
identified
diverse
neurologic
conditions
including
stroke,
trauma,
and
anoxia,
increased
utilization
continuous
(cEEG)
has
potentially
harmful
activity
even
patients
without
overt
clinical
signs
or
diagnoses.
Manual
annotation
by
expert
neurophysiologists
a
major
resource
limitation
investigating
prognostic
therapeutic
implications
these
patterns
expanding
use
to
broader
set
who
are
likely
benefit.
Artificial
intelligence
(AI)
already
demonstrated
success
guiding
cEEG
allocation
for
at
risk
seizures,
its
potential
uses
neurocritical
care
alongside
improvements
AI
itself.
We
review
both
current
EEG-guided
as
well
ongoing
research
directions
automated
seizure
ischemia
detection,
prognostication,
guidance
medical
surgical
treatment.