Communications Medicine,
Год журнала:
2024,
Номер
4(1)
Опубликована: Ноя. 26, 2024
Diagnosing
complex
illnesses
like
Myalgic
Encephalomyelitis/Chronic
Fatigue
Syndrome
(ME/CFS)
is
complicated
due
to
the
diverse
symptomology
and
presence
of
comorbid
conditions.
ME/CFS
patients
often
present
with
multiple
health
issues,
therefore,
incorporating
comorbidities
into
research
can
provide
a
more
accurate
understanding
condition's
symptomatology
severity,
better
reflect
real-life
patient
experiences.
We
performed
association
studies
machine
learning
on
1194
individuals
blood
plasma
nuclear
magnetic
resonance
(NMR)
metabolomics
profiles,
seven
exclusive
cohorts:
hypertension
(n
=
13,559),
depression
2522),
asthma
6406),
irritable
bowel
syndrome
859),
hay
fever
3025),
hypothyroidism
1226),
migraine
1551)
non-diseased
control
group
53,009).
lipoprotein
perspective
pathophysiology,
highlighting
gender-specific
differences
identifying
overlapping
associations
conditions,
specifically
surface
lipids,
ketone
bodies
from
168
significant
individual
biomarker
associations.
Additionally,
we
searched
for,
trained,
optimised
algorithm,
resulting
in
predictive
model
using
19
baseline
characteristics
nine
NMR
biomarkers
which
could
identify
an
AUC
0.83
recall
0.70.
A
multi-variable
score
was
subsequently
derived
same
28
features,
exhibited
~2.5
times
greater
than
top
biomarker.
This
study
provides
end-to-end
analytical
workflow
that
explores
potential
clinical
utility
scores
may
have
for
other
difficult
diagnose
illness
severe
fatigue
without
known
cause.
Further
symptoms
overlap
medical
problems
making
diagnosis
difficult.
wanted
find
way
easily
people
this
condition,
so
used
data
UK
Biobank
compare
who
had
problems.
developed
mathematical
calculation,
basic
factors
markers,
classify
non-ME/CFS
correctly
83%
time,
recognise
condition
70%
time.
lead
serve
as
example
diseases
lacking
definite
laboratory
testing.
Huang
et
al.
train
optimize
predict
cases
Biobank.
works
heterogenous
condition.
World Journal of Emergency Medicine,
Год журнала:
2025,
Номер
16(3), С. 248 - 248
Опубликована: Янв. 1, 2025
Community-acquired
pneumonia
(CAP)
represents
a
significant
public
health
concern
due
to
its
widespread
prevalence
and
substantial
healthcare
costs.
This
study
was
utilize
an
integrated
proteomic
metabolomic
approach
explore
the
mechanisms
involved
in
severe
CAP.
We
proteomics
metabolomics
data
identify
potential
biomarkers
for
early
diagnosis
of
Plasma
samples
were
collected
from
46
CAP
patients
(including
27
with
19
non-severe
CAP)
healthy
controls
upon
admission.
A
comprehensive
analysis
combined
then
performed
elucidate
key
pathological
features
associated
severity.
The
metabolic
signature
markedly
different
between
CAPs
controls.
Pathway
changes
revealed
complement
coagulation
cascades,
ribosome,
tumor
necrosis
factor
(TNF)
signaling
pathway
lipid
process
as
contributors
Furthermore,
alterations
metabolism,
including
sphingolipids
phosphatidylcholines
(PCs),
dysregulation
cadherin
binding
observed,
potentially
contributing
development
Specifically,
within
group,
sphingosine-1-phosphate
(S1P)
apolipoproteins
(APOC1
APOA2)
levels
downregulated,
while
S100P
level
significantly
upregulated.
may
complexity
severity
inform
improved
diagnostic
tools.
Journal of Proteome Research,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 19, 2025
In
the
present
study,
we
investigated
biochemical,
hematological,
lipidomic,
and
metabolomic
alterations
associated
with
different
SAR-CoV-2
variants
of
concern
(VOCs),
such
as
WT,
α,
β,
γ,
δ,
well
their
impact
on
COVID-19
severity.
Across
first
second
waves
in
India,
a
machine
learning
approach
was
used
3134
patients,
nine
critical
biochemical
hematological
parameters,
namely,
C-reactive
protein
(CRP),
D-dimer,
ferritin,
neutrophil,
WBC
count,
lymphocyte,
urea,
creatine,
lactate
dehydrogenase
(LDH),
were
identified.
Furthermore,
through
metabolic
lipidomic
profiles
lung
colon
cells
transfected
spike
VOCs,
notable
dysregulation
exhibited
by
delta
variant
correlated
characteristic
pathways
catecholamine
thyroid
hormone
synthesis.
A
corroborating
meta-analysis
also
highlighted
involvement
urea
amino
acid
metabolism
pathways.
Overall,
our
study
provides
crucial
insights
into
disruptions
caused
contributing
to
better
understanding
pathogenesis
development
targeted
interventions.
Frontiers in Immunology,
Год журнала:
2025,
Номер
16
Опубликована: Май 22, 2025
Little
is
known
about
the
acute
and
long-term
sequelae
of
COVID-19
its
pathophysiology
in
African
patients,
who
are
to
have
a
distinct
immunological
profile
compared
Caucasian
populations.
Here,
we
established
protein
signatures
define
severe
outcomes
determined
whether
unique
during
first
week
illness
predict
risk
post-acute
(Long
COVID)
low-income
country
(LIC)
setting.
Using
Olink
inflammatory
panel,
measured
abundance
92
proteins
plasma
patients
(n=55)
non-COVID-19
individuals
(n=23).
We
investigated
(n=22)
asymptomatic
or
mild/moderate
cases
(n=33),
controls.
Levels
SLAMF1,
CCL25,
IL2RB,
IL10RA,
IL15RA,
IL18
CST5
were
significantly
upregulated
with
critical
negative
for
COVID-19.
The
cohort
was
followed
an
average
20
months,
23
developed
Long
COVID,
based
on
WHO's
case
definition,
while
32
recovered
fully.
Whereas
levels
TNF,
TSLP,
IL18,
ADA,
CXCL9,
CXCL10,
IL17C,
NT3
at
phase
associated
increased
COVID
risk,
TRANCE
reduced
developing
COVID.
Protein
also
predicted
risk.
Patients
exhibited
proteomic
signatures.
Unravelling
before
advent
may
contribute
designing
novel
interventions
diagnosing,
treating,
monitoring
SARS-CoV-2
infection
consequences.
PLoS ONE,
Год журнала:
2024,
Номер
19(6), С. e0304522 - e0304522
Опубликована: Июнь 5, 2024
Background
A
subset
of
individuals
(10–20%)
experience
post-COVID
condition
(PCC)
subsequent
to
initial
SARS-CoV-2
infection,
which
lacks
effective
treatment.
PCC
carries
a
substantial
global
burden
associated
with
negative
economic
and
health
impacts.
This
study
aims
evaluate
the
association
between
plasma
taurine
levels
self-reported
symptoms
adverse
clinical
outcomes
in
patients
PCC.
Methods
findings
We
analyzed
proteome
metabolome
117
during
their
acute
COVID-19
hospitalization
at
convalescence
phase
six-month
post
infection.
Findings
were
compared
28
age
sex-matched
healthy
controls.
Plasma
negatively
correlated
markers
inflammation,
tryptophan
metabolism,
gut
dysbiosis.
Stratifying
based
on
trajectories
follow-up
revealed
significant
events.
Increase
transition
reduction
events
independent
comorbidities
severity.
In
multivariate
analysis,
increased
level
was
marked
protection
from
hazard
ratio
0.13
(95%
CI:
0.05–0.35;
p<0.001).
Conclusions
Taurine
emerges
as
promising
predictive
biomarker
potential
therapeutic
target
supplementation
has
already
demonstrated
benefits
various
diseases
warrants
exploration
large-scale
trials
for
alleviating
Communications Medicine,
Год журнала:
2024,
Номер
4(1)
Опубликована: Ноя. 26, 2024
Diagnosing
complex
illnesses
like
Myalgic
Encephalomyelitis/Chronic
Fatigue
Syndrome
(ME/CFS)
is
complicated
due
to
the
diverse
symptomology
and
presence
of
comorbid
conditions.
ME/CFS
patients
often
present
with
multiple
health
issues,
therefore,
incorporating
comorbidities
into
research
can
provide
a
more
accurate
understanding
condition's
symptomatology
severity,
better
reflect
real-life
patient
experiences.
We
performed
association
studies
machine
learning
on
1194
individuals
blood
plasma
nuclear
magnetic
resonance
(NMR)
metabolomics
profiles,
seven
exclusive
cohorts:
hypertension
(n
=
13,559),
depression
2522),
asthma
6406),
irritable
bowel
syndrome
859),
hay
fever
3025),
hypothyroidism
1226),
migraine
1551)
non-diseased
control
group
53,009).
lipoprotein
perspective
pathophysiology,
highlighting
gender-specific
differences
identifying
overlapping
associations
conditions,
specifically
surface
lipids,
ketone
bodies
from
168
significant
individual
biomarker
associations.
Additionally,
we
searched
for,
trained,
optimised
algorithm,
resulting
in
predictive
model
using
19
baseline
characteristics
nine
NMR
biomarkers
which
could
identify
an
AUC
0.83
recall
0.70.
A
multi-variable
score
was
subsequently
derived
same
28
features,
exhibited
~2.5
times
greater
than
top
biomarker.
This
study
provides
end-to-end
analytical
workflow
that
explores
potential
clinical
utility
scores
may
have
for
other
difficult
diagnose
illness
severe
fatigue
without
known
cause.
Further
symptoms
overlap
medical
problems
making
diagnosis
difficult.
wanted
find
way
easily
people
this
condition,
so
used
data
UK
Biobank
compare
who
had
problems.
developed
mathematical
calculation,
basic
factors
markers,
classify
non-ME/CFS
correctly
83%
time,
recognise
condition
70%
time.
lead
serve
as
example
diseases
lacking
definite
laboratory
testing.
Huang
et
al.
train
optimize
predict
cases
Biobank.
works
heterogenous
condition.