Impact of COVID-19 on mucormycosis presentation and laboratory values: A comparative analysis
Sepideh Hejazi,
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Ali Gholampour Kargar,
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Sahar Ravanshad
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et al.
PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(5), P. e0321897 - e0321897
Published: May 2, 2025
Background
The
COVID-19
pandemic
has
led
to
an
alarming
increase
in
mucormycosis
coinfections
and
its
rapid
progression.
overlapping
risk
factors
symptoms
between
further
complicate
prompt
detection,
which
is
crucial
for
patient
survival.
This
study
aims
investigate
potential
differences
progression,
initial
symptom
presentation,
laboratory
value
alterations
patients
with
history
enhance
diagnostic
accuracy
improve
outcomes
this
complex
clinical
scenario.
Methodology
retrospective
cohort
study,
conducted
from
April
1,
2021,
March
31,
2022,
examined
102
diagnosed
at
two
primary
teaching
hospitals.
Patients
were
categorized
into
groups
based
on
history.
Variables
included
demographic
information,
parameters,
results,
outcomes.
compared
studies
presentation
history-positive
history-negative
groups,
a
particular
focus
mortality
rates
associated
comorbidities
such
as
diabetes,
cancer
immunosuppressive
treatment.
Results
Initial
presentations
differed
significantly,
eneralized
Estimating
Equations
(GEE)
analysis,
adjusted
comorbidities,
revealed
was
increased
platelet
counts
(P
=
0.0311)
decreased
facial
swelling
0.049)
fever
reporting
<
0.001).
Cancer
history,
treatment
also
showed
significant
associations
various
parameters.
Laboratory
analysis
without
group
lower
WBC
0.002),
higher
hemoglobin
levels
0.001)
controls.
Diabetes
more
prevalent
patients,
while
common
Conclusion
reveals
intricate
relationships
mucormycosis,
challenging
earlier
findings.
Mucormycosis
exhibited
altered
presentation.
research
highlights
varied
patterns
across
subgroups
underscores
the
complexity
of
interactions
COVID-19,
cancer,
diabetes
cases.
These
findings
advocate
multivariate
analytical
approaches
better
understand
these
multifaceted
relationships.
Language: Английский
Bioinformatics and system biology approach to discover the common pathogenetic processes between COVID-19 and chronic hepatitis B
PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(5), P. e0323708 - e0323708
Published: May 23, 2025
Introduction
The
ongoing
coronavirus
disease
2019
(COVID-19)
pandemic,
caused
by
the
severe
acute
respiratory
syndrome
2
(SARS-CoV-2),
presents
a
significant
global
public
health
threat.
Concurrently,
hepatitis
B
virus
(HBV)
remains
challenge.
While
previous
studies
have
indicated
an
association
between
COVID-19
and
chronic
B,
common
underlying
pathogenesis
of
these
diseases
incompletely
understood.
Methods
To
investigate
shared
molecular
mechanisms
HBV
infection
COVID-19,
comprehensive
investigation
was
conducted
using
bioinformatics
systems
biology.
Specifically,
we
utilized
RNA-seq
datasets
(GSE196822
GSE83148)
to
identify
differentially
expressed
genes
(DEGs)
associated
with
both
SARS-CoV-2
infection.
Subsequently,
DEGs
were
pathways,
hub
genes,
transcriptional
regulatory
networks,
potential
drugs.
differential
expression
in
verified
GSE171110
GSE94660
datasets,
respectively.
Results
From
106
identified,
immune-related
pathways
found
play
role
development
progression
COVID-19.
Protein-protein
interaction
(PPI)
network
analysis
revealed
8
genes:
CDK1
,
E2F7
E2F8
TYMS
KIF20A
CENPE
TPX2
HMMR
CD8A
GZMA
.
In
validation
set,
statistically
group
compared
healthy
control
group.
Transcriptional
identified
155
microRNAs
(miRNAs)
43
transcription
factors
(TFs)
as
signals.
Notably,
therapeutic
drugs
for
including
progesterone,
estradiol,
dasatinib,
aspirin,
etoposide,
irinotecan
hydrochloride,
phorbol
12-myristate
13-acetate,
lucanthone,
calcitriol.
Conclusion
This
research
elucidates
targets,
signaling
promising
small
molecule
compounds
that
could
aid
treatment
Language: Английский