Distinct virologic trajectories in chronic hepatitis B identify heterogeneity in response to nucleos/tide analogue therapy
JHEP Reports,
Год журнала:
2024,
Номер
7(1), С. 101229 - 101229
Опубликована: Окт. 9, 2024
Highlights•Virologic
responses
to
NA
therapy
in
chronic
hepatitis
B
patients
show
significant
variability.•Five
distinct
virologic
trajectory
classes
with
clinical,
laboratory
and
demographic
features
are
identified.•Over
20%
of
exhibit
suboptimal
virological
treatment.•Complete
suppression
for
on
current
standard
antiviral
treatment
can
be
slow.•Slow
is
associated
a
twofold
increased
risk
fibrosis/cirrhosis.AbstractBackground
&
AimsThe
dynamics
HBV
viral
load
(VL)
(CHB)
nucleos/tide
analogue
(NA)
its
relationship
liver
disease
poorly
understood.
We
aimed
study
longitudinal
VL
patterns
their
associations
CHB
clinical
outcomes.MethodsUtilising
large
scale,
routinely
collected
electronic
health
records
from
six
centres
England,
collated
by
the
National
Institute
Health
Care
Research
Informatics
Collaborative
(NIHR
HIC),
we
applied
latent
class
mixed
models
investigate
adults
receiving
treatment.
assessed
alanine
transaminase
(ALT),
fibrosis/cirrhosis.ResultsWe
retrieved
data
1885
(median
follow-up
6.2
years,
interquartile
range
(IQR)
3.7-9.3
years),
21,691
measurements
10
per
patient,
IQR
5-17).
Five
were
identified
derivation
cohort
(n=1367,
discrimination:
0.93,
entropy:
0.90):
1
'long
term
suppression'
(n=827,
60.5%),
2
'timely
(n=254,
18.6%),
3
'persistent
moderate
viraemia'
(n=140,
10.2%),
4
high-level
(n=44,
3.2%),
5
'slow
(n=102,
7.5%).
The
model
demonstrated
discrimination
0.93
entropy
0.88
validation
(n=518).
ALT
decreased
variably
over
time
VL-suppressed
groups
(classes
1,
2,
5;
all
p<0.001),
but
did
not
significantly
improve
those
persistent
viraemia
3,
4).
Patients
had
2-fold
hazards
fibrosis/cirrhosis
compared
(adjusted
hazard
ratio,
2.00;
95%
CI,
1.33-3.02).ConclusionsHeterogeneity
exists
response
patients,
showing
potentially
responses.
Slow
progression.Graphical
abstract
Язык: Английский
Classification of virologic trajectories during nucleos/tide analogue treatment of hepatitis B virus (HBV) infection
medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Дек. 1, 2023
Abstract
Background
&
Aims
The
dynamics
of
HBV
viral
load
(VL)
in
patients
with
chronic
hepatitis
B
(CHB)
on
nucleos/tide
analogue
(NA)
treatment
and
its
relationship
liver
disease
are
poorly
understood.
We
aimed
to
study
longitudinal
VL
patterns
their
associations
CHB
clinical
outcomes.
Methods
Utilising
large
scale,
routinely
collected
electronic
health
records
from
six
centres
England,
collated
by
the
National
Institute
for
Health
Care
Research
Informatics
Collaborative
(NIHR
HIC),
we
applied
latent
class
mixed
models
investigate
trajectory
adults
receiving
NA
treatment.
assessed
alanine
transaminase
(ALT),
fibrosis/cirrhosis.
Results
retrieved
data
1885
(median
follow-up
6.2
years,
interquartile
range
(IQR)
3.7-9.3
years),
21,691
measurements
10
per
patient,
IQR
5-17).
Five
classes
were
identified
derivation
cohort
(n=1367,
discrimination:
0.93,
entropy:
0.90):
1
‘long
term
suppression’
(n=827,
60.5%),
2
‘timely
virological
(n=254,
18.6%),
3
‘persistent
moderate
viraemia’
(n=140,
10.2%),
4
high-level
(n=44,
3.2%),
5
‘slow
(n=102,
7.5%).
model
demonstrated
a
discrimination
0.93
entropy
0.88
validation
(n=518).
ALT
decreased
variably
over
time
VL-suppressed
groups
(classes
1,
2,
5;
all
p<0.001),
but
did
not
significantly
improve
those
persistent
viraemia
3,
4).
Patients
had
2-fold
increased
hazards
fibrosis/cirrhosis
compared
(adjusted
hazard
ratio,
2.00;
95%
CI,
1.33-3.02).
Conclusions
Heterogeneity
exists
response
therapy
patients,
20%
showing
potentially
suboptimal
responses.
Slow
suppression
is
associated
progression.
Язык: Английский