Rheumatology & autoimmunity,
Journal Year:
2024,
Volume and Issue:
4(3), P. 174 - 179
Published: May 27, 2024
Abstract
Background
Polymyalgia
rheumatica
(PMR)
is
an
inflammatory
disease
that
affects
the
older
adult
population.
The
aim
of
this
study
was
to
investigate
risk
and
prognosis
associated
with
coronavirus
2019
(COVID‐19)
infection
among
patients
diagnosed
PMR
during
predominance
Omicron
variant.
Methods
In
retrospective
study,
we
included
a
cohort
who
met
2012
European
League
Against
Rheumatism/American
College
Rheumatology
classification
criteria
or
1982
diagnostic
tracked
their
progress
over
time.
diagnosis
COVID‐19
based
on
clinical
manifestations
laboratory
tests.
We
collected
demographic
information,
activity,
treatment
data,
data
related
COVID‐19.
Results
total,
101
were
enrolled.
Most
exhibited
low
activity.
Of
total
cohort,
81
(80.2%)
categorized
as
individuals
COVID‐19,
while
remaining
20
(19.8%)
not
Among
65
presence
antigen,
16
tested
positive
for
RNA.
classified
having
mild
(72,
88.9%).
Two
cases
identified
within
confirmed
infected
group,
resulting
in
recurrence
rate
2.5%
(2/81).
Conversely,
no
relapses
observed
non‐infected
group
(0/20).
our
multivariate
logistic
regression
analysis,
found
pre‐COVID‐19
activity
independent
factor
(odds
ratio
=
30.00,
95%
confidence
interval:
2.137–421.117,
p
0.012).
Conclusion
increased
susceptibility
may
be
influenced
by
pre‐existing
PMR.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 8, 2024
Introduction
Severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2)
may
trigger
autoimmune
disease
(AD)
through
initial
innate
immune
activation
with
subsequent
aberrations
in
adaptive
cells
leading
to
AD.
While
there
are
multiple
reports
of
incident
AD
diagnosed
after
COVID-19,
the
risk
context
key
circulating
strains
is
unknown.
Methods
TriNetX,
a
global,
federated,
health
research
network
providing
access
electronic
medical
records
across
74
healthcare
organizations,
was
utilized
define
an
adult
cohort
between
January
1,
2020,
and
March
3,
2023.
Exposure
defined
as
COVID-19
diagnosis
(ICD-10
code
or
positive
laboratory
test).
Age-
sex-propensity
score-matched
controls
never
had
diagnosed.
Outcomes
were
assessed
1
month
year
index
date.
Patients
prior
within
date
excluded
from
primary
analysis.
Incidence
ratios
each
assessed.
Results
A
total
3,908,592
patients
included.
Of
24
assessed,
adjusted
for
eight
who
higher
compared
those
no
COVID-19.
Cutaneous
vasculitis
(adjusted
hazard
ratio
(aHR):
1.82;
95%
CI
1.55–2.13),
polyarteritis
nodosa
(aHR:
1.76;
1.15–2.70),
hypersensitivity
angiitis
1.64;
1.12–2.38)
highest
ratios.
Overall,
psoriasis
(0.15%),
rheumatoid
arthritis
(0.14%),
type
diabetes
(0.13%)
incidence
during
study
period,
these,
more
likely
The
any
lower
if
when
Omicron
variants
predominant
strains.
antinuclear
antibody
predictive
Discussion
SARS-CoV-2
be
potential
some
AD,
but
decrease
time
given
apparent
infection
variants.
Human Vaccines & Immunotherapeutics,
Journal Year:
2024,
Volume and Issue:
20(1)
Published: April 2, 2024
We
conducted
a
national
in-depth
analysis
including
pharmacovigilance
reports
and
clinical
study
to
assess
the
reporting
rate
(RR)
determine
profile
of
polymyalgia
rheumatica
(PMR)
giant
cell
arteritis
(GCA)
in
COVID-19-vaccinated
individuals.
First,
based
on
French
database,
we
estimated
RR
PMR
GCA
cases
individuals
aged
over
50
who
developed
their
initial
symptoms
within
one
month
receiving
BNT162b2
mRNA,
mRNA-1273,
ChAdOx1
nCoV-19,
Ad26.COV2.S
vaccines.
then
nationwide
survey
gather
profiles,
therapeutic
management,
follow-up
data
from
registered
study.
A
total
70
854
684
COVID-19
vaccine
doses
were
administered
25
260
485
adults,
among
which,
179
(RR
7.
1
cases/1
000
persons)
54
2.
have
been
reported.
The
allowed
characterization
60
35
cases.
Median
time
onset
first
was
10
(range
2–30)
7
2–25)
days
for
GCA,
respectively.
Phenotype,
GCA-related
ischemic
complications
-large
vessel
vasculitis
as
well
management
seemed
similar
according
number
shots
received
when
compared
literature
unvaccinated
population.
Although
rare,
short
between
immunization
suggests
temporal
association.
Physician
should
be
aware
this
potential
vaccine-related
phenomenon.
Exploration of Immunology,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 33
Published: Jan. 31, 2024
The
coronavirus
disease
2019
(COVID-19)
pandemic
cost
7–8
million
deaths
worldwide,
creating
an
unprecedented
health
and
economic
crisis.
Affecting
700
people
globally,
the
magnitude
of
this
is
far
from
anything
that
humanity
has
encountered
in
recent
times.
A
detailed
investigation
revealed
more
than
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
virus,
hyperactive
immune
system
mediated
injury
as
real
cause
mortality.
Cytokine
storm
following
viral
infection
leads
to
surge
proinflammatory
cytokines
resulting
distress
(ARDS)
lung
injury.
Anti-inflammatory
intervention
with
anti-interleukin-6
(anti-IL-6)
receptor
monoclonal
antibodies
(mAbs;
e.g.,
sarilumab
tocilizumab)
anti-IL-6
mAbs
(i.e.,
siltuximab)
and/or
steroid-based
approach
substantial
protection
prevent
death
thereby
implying
role
inflammation
COVID-19.
In
review,
authors
have
summarized
dysregulated
COVID-19
infection,
investigating
detail
virus-host
cross
talks
presenting
possibilities
therapeutic
intervention.
Advances in Rheumatology,
Journal Year:
2025,
Volume and Issue:
65(1)
Published: Jan. 22, 2025
Abstract
Objectives
To
compare
the
impact
of
COVID-19
on
clinical
status
and
psychological
distress
patients
with
immune-mediated
rheumatic
disease
(IMRD)
caused
by
SARS-CoV-2
infection
that
noninfected
IMRD
controls
during
a
6-month
follow-up
period.
Methods
The
ReumaCoV
Brazil
is
longitudinal
study
designed
to
follow
for
6
months
after
(patients)
compared
without
(controls).
Clinical
data,
activity
measurements
current
treatments
regarding
outcomes
were
evaluated
in
all
patients.
Disease
was
assessed
through
validated
tools
at
inclusion
3
post-COVID-19.
Fatigue,
using
FACIT-F
(Functional
Assessment
Chronic
Illness
Therapy)
distress,
DASS
21
(Depression,
Anxiety
Stress
Scale
−
Items),
used
both
groups.
significance
level
set
as
p
<
0.05,
95%
confidence
interval.
Results
A
total
601
evaluated—321
(IMRD
+
patients)
280
COVID-19-
patients)—who
predominantly
female
similar
median
ages.
assessment
over
showed
no
significant
difference
between
cases
controls.
Although
mean
scores
did
not
differ
significantly,
some
reported
worsened
post-COVID-19,
particularly
rheumatoid
arthritis
(RA)
(32.2%)
systemic
lupus
erythematosus
(SLE)
(23.3%).
Post-COVID-19
worsening
RA
correlated
medical
global
(MGA)
CDAI
scores,
moderate
large
effect
size.
Diabetes
mellitus
positive
association
(OR
=
7.15),
while
TNF
inhibitors
had
protective
0.51).
depression,
anxiety,
stress
significantly
greater
than
Worse
post-COVID-19
worse
DASS-21
No
associations
found
activity,
or
DASS-21.
Conclusions
exhibited
fatigue,
stress,
which
can
be
mistaken
despite
having
scores.
variability
reports
flares
potential
triggering
autoimmune
manifestations
underscore
need
detailed
comprehensive
approach
managing
them.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: April 27, 2025
Abstract
The
safety
profile
of
COVID-19
vaccines
is
well-established,
yet
the
widespread
immunization
campaign
has
led
to
an
increase
in
reported
cases
Immune-Mediated
and
Rheumatic
Diseases
(IMDRs).
This
study
aimed
assess
reporting
Adverse
Events
Following
Immunization
(AEFIs)
related
IMDRs
after
vaccination.
We
analyzed
all
individual
case
reports
(ICSRs)
authorized
European
Union
(i.e.,
tozinameran,
elasomeran,
ChAdOx1-S
NCoV-19,
Ad26.Cov2.S)
registered
EudraVigilance
(EV)
database
from
January
1,
2021,
October
23,
2023.
Our
analysis
identified
ICSRs
with
events
indicative
conducted
disproportionality
Reporting
Odds
Ratio
(ROR)
95%
CI)
examine
frequency
different
IMDR
types
linked
each
vaccine.
In
total,
45,352
at
least
one
AEFI
associated
rheumatic
or
autoimmune
conditions,
54%
them
implicating
tozinameran
as
suspected
More
than
half
AEFIs
were
classified
serious,
approximately
45%
remaining
unresolved.
most
frequently
conditions
other
immune-mediated
diseases,
followed
by
arthritis,
vasculitis,
systemic
lupus
erythematosus,
tendinopathies.
suggested
that
mRNA
may
be
more
new
diseases.
Stratified
revealed
significant
associations
for
ChAd,
particularly
vasculitis
tendinopathies,
only
when
compared
Ad26.Cov2.S.
Real-world
pharmacovigilance
data
suggest
diseases
under-reported
following
vaccination,
highlighting
need
further
research
better
understand
underlying
mechanisms.
findings
this
studies
investigate
these
results
greater
depth.
RMD Open,
Journal Year:
2025,
Volume and Issue:
11(2), P. e005138 - e005138
Published: April 1, 2025
Background
While
several
studies
have
reported
some
cases
of
polymyalgia
rheumatica
(PMR)
following
COVID-19
vaccination,
using
large
databases
are
lacking.
Objectives
To
investigate
the
risk
PMR
after
vaccination
self-controlled
case
series
(SCCS)
analysis
Methods
We
used
National
Health
Insurance
Database,
linked
with
registry
between
February
2021
and
August
2023,
to
identify
adults
aged
50
years
or
older
who
received
at
least
one
dose
vaccine
subsequently
diagnosed
within
observation
period,
defined
as
240
days
first
vaccine.
The
window
was
28
each
control
encompassed
remainder
period.
Incidence
rate
ratios
(IRRs)
were
estimated
conditional
Poisson
regression
95%
CIs,
stratified
by
type.
Results
Among
44
818
078
recipients,
376
patients
PMR.
indicated
that
not
associated
an
increased
(IRR,
0.74;
CI
0.59
0.94).
Rather,
slightly
reduced
(0.52;
0.34
0.79),
no
significant
association
other
doses
(0.83;
1.16
for
second
dose,
0.77,
0.48
1.25
third
dose).
Conclusion
In
this
nationwide
SCCS,
there
vaccination.
these
findings
support
safety
vaccines,
interpretation
decreased
should
be
cautious.
Pediatric Rheumatology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: May 14, 2025
During
the
COVID-19
pandemic
there
were
reports
of
an
increased
association
between
COVID
19
and
various
autoimmune
diseases
(AID)
in
adults.
This
study
aims
to
investigate
incidence
AIDs
children
before
during
explores
potential
links
SARS-CoV-2
vaccination.
We
analyzed
493,705
anonymized
medical
records
from
Maccabi
Healthcare
Services,
Israel's
second-largest
healthcare
provider,
AID
2014-2022.
The
period
was
divided
into
three
phases:
two
pre-pandemic
phases
equal
duration
(A
B)
a
phase
(C).
Of
4,596
(0.9%)
patients
diagnosed
with
cohort,
rates
0.9%
for
Group
A
(2014-2016),
1.0%
B
(2017-2019),
C
(2020-2022)
(p
=
0.13).
Logistic
regression
showed
no
significant
differences
overall
disease
pre-COVID
periods.
Notably,
specific
conditions
like
celiac
reduced
(OR
0.8309,
p
0.0071)
while
arthritis
significantly
more
common
Groups
B.
Additionally,
diagnosis
not
associated
risk
(HR
1.092,
0.491);
however,
receiving
at
least
one
vaccine
linked
higher
1.2323,
0.0033).
Our
findings
suggest
that
new-onset
remained
relatively
stable
pandemic.
indicates
vaccination
developing
diseases,
necessitating
further
research
elucidate
long-term
effects
pediatric
population.