The
COVID-19
pandemic
has
presented
significant
challenges
to
healthcare
systems
worldwide,
with
the
management
of
vulnerable
patient
populations,
such
as
those
rheumatic
diseases
(RD),
being
particular
concern.
This
study
aimed
assess
impact
on
patients
RD,
focusing
disease
course,
vaccination,
and
effect
concomitant
therapy.
results
indicate
that
low
activity
inflammatory
arthritis
(IA)
or
remission
may
serve
a
reliable
predictor
course
outcomes,
56.3%
exhibiting
mild
infection
course.
Synthetic
disease-modifying
drugs
(DMARDs),
including
both
biological
targeted
agents,
be
useful
in
achieving
this
goal.
Clinical
manifestations
IA
differed
from
control
group,
lower
incidence
fever
above
38
ºС
(OR
2.84;
95%
CI
1.24
–
6.51)
higher
frequency
myalgia
0.39;
0.17
0.89).
All
other
symptoms
occurred
same
frequency.
use
vitamin
D3
prescription
scheme
proposed
I-PREVENT:
COVID
PROTECTION
PROTOCOL
FLCCC
protocol
also
effective
reducing
symptom
duration
(from
41.7
±
11.4
days
32.4
9.6
days,
p
=
0.04)
leads
greater
decrease
level
interleukin-6
(18.2
5.9
pg/ml
vs
23.7
7.2
pg/ml)
treatment
increasing
IL-4
(2.74
0.83
2.33
0.61
pg/ml),
which
is
considered
positive
marker.
Vaccination
against
safe
for
RD
immune
response
formation,
albeit
less
pronounced
than
healthy
individuals
(360
110
BAU/ml
470
150
BAU/ml,
p=0.01,
reference
values
10
BAU/ml).
Notably,
spondyloarthritis
(SpA)
general
suppression
humoral
response,
exhibited
highest
production
IgG
class
antibodies
SARS-CoV-2
Spike
protein
when
treated
DMARD
sulfasalazine:
566
159
321
98
tumor
necrosis
factor
inhibitor
p<0.0001
354
102
methotrexate
p=0.0036.
No
intake
coronavirus
was
observed
RD.
Ultimately,
optimal
during
involves
primary
Reviews in Endocrine and Metabolic Disorders,
Journal Year:
2021,
Volume and Issue:
23(2), P. 265 - 277
Published: July 29, 2021
Abstract
Vitamin
D,
best
known
for
its
role
in
skeletal
health,
has
emerged
as
a
key
regulator
of
innate
immune
responses
to
microbial
threat.
In
cells
such
macrophages,
expression
CYP27B1,
the
25-hydroxyvitamin
D
1α-hydroxylase,
is
induced
by
immune-specific
inputs,
leading
local
production
hormonal
1,25-dihydroxyvitamin
(1,25D)
at
sites
infection,
which
turn
directly
induces
genes
encoding
antimicrobial
peptides.
signaling
active
upstream
and
downstream
pattern
recognition
receptors,
promote
front-line
responses.
Moreover,
1,25D
stimulates
autophagy,
mechanism
critical
control
intracellular
pathogens
M.
tuberculosis
.
Strong
laboratory
epidemiological
evidence
links
vitamin
deficiency
increased
rates
conditions
dental
caries,
well
inflammatory
bowel
diseases
arising
from
dysregulation
handling
intestinal
flora.
also
cascades
that
antiviral
immunity;
1,25D-induced
peptide
CAMP/LL37,
originally
characterized
antibacterial
properties,
component
Poor
status
associated
with
greater
susceptibility
viral
infections,
including
those
respiratory
tract.
Although
severity
COVID-19
pandemic
been
alleviated
some
areas
arrival
vaccines,
it
remains
important
identify
therapeutic
interventions
reduce
disease
mortality,
accelerate
recovery.
This
review
outlines
our
current
knowledge
mechanisms
action
system.
It
provides
an
assessment
potential
supplementation
infectious
diseases,
up-to-date
analysis
putative
benefits
ongoing
crisis.
Nutrients,
Journal Year:
2022,
Volume and Issue:
14(9), P. 1862 - 1862
Published: April 29, 2022
A
higher
risk
for
severe
clinical
courses
of
coronavirus
disease
2019
(COVID-19)
has
been
linked
to
deficiencies
several
micronutrients.
We
therefore
studied
the
prevalence
eight
different
micronutrients
in
a
cohort
hospitalized
COVID-19-patients.
Nutrients,
Journal Year:
2025,
Volume and Issue:
17(3), P. 599 - 599
Published: Feb. 6, 2025
Clinical
trials
consistently
demonstrate
an
inverse
correlation
between
serum
25-hydroxyvitamin
D
[25(OH)D;
calcifediol]
levels
and
the
risk
of
symptomatic
SARS-CoV-2
disease,
complications,
mortality.
This
systematic
review
(SR),
guided
by
Bradford
Hill’s
causality
criteria,
analyzed
294
peer-reviewed
manuscripts
published
December
2019
November
2024,
focusing
on
plausibility,
consistency,
biological
gradient.
Evidence
confirms
that
cholecalciferol
(D3)
calcifediol
significantly
reduce
hospitalizations,
mortality,
with
optimal
effects
above
50
ng/mL.
While
vitamin
requires
3–4
days
to
act,
shows
within
24
h.
Among
329
trials,
only
11
(3%)
showed
no
benefit
due
flawed
designs.
At
USD
2/patient,
D3
supplementation
is
far
cheaper
than
hospitalization
costs
more
effective
standard
interventions.
SR
establishes
a
strong
relationship
25(OH)D
vulnerability,
meeting
criteria.
Vitamin
infections,
deaths
~50%,
outperforming
all
patented,
FDA-approved
COVID-19
therapies.
With
over
300
confirming
these
findings,
waiting
for
further
studies
unnecessary
before
incorporating
them
into
clinical
protocols.
Health
agencies
scientific
societies
must
recognize
significance
results
incorporate
prophylaxis
early
treatment
protocols
similar
viral
infections.
Promoting
safe
sun
exposure
adequate
communities
maintain
40
ng/mL
(therapeutic
range:
40–80
ng/mL)
strengthens
immune
systems,
reduces
hospitalizations
deaths,
lowers
healthcare
costs.
When
exceed
70
ng/mL,
taking
K2
(100
µg/day
or
800
µg/week)
alongside
helps
direct
any
excess
calcium
bones.
The
recommended
dosage
(approximately
IU/kg
body
weight
non-obese
adult)
50–100
cost-effective
disease
prevention,
ensuring
health
outcomes.
Life,
Journal Year:
2025,
Volume and Issue:
15(5), P. 733 - 733
Published: April 30, 2025
Vitamin
D
has
emerged
as
a
potential
modulator
of
immune
responses,
sparking
interest
in
its
role
COVID-19
susceptibility
and
clinical
outcomes.
This
review
synthesizes
current
evidence
explores
immunological
insights
into
the
relationship
between
vitamin
levels
infection
severity.
Epidemiological
studies
indicate
an
inverse
correlation
deficiency
increased
risk
severe
disease,
hospitalization,
mortality
patients.
Immunologically,
exerts
regulatory
effects
on
both
innate
adaptive
immunity,
enhancing
antimicrobial
defense
mechanisms,
reducing
excessive
inflammatory
potentially
mitigating
cytokine
storm
events
observed
cases.
Despite
promising
observational
data,
trials
evaluating
supplementation
have
shown
mixed
results,
underscoring
need
for
standardized
dosing
regimens
patient
stratification.
Future
research
should
focus
large-scale
randomized
controlled
to
conclusively
determine
therapeutic
optimal
strategies
managing
COVID-19.
Biology,
Journal Year:
2024,
Volume and Issue:
13(10), P. 831 - 831
Published: Oct. 16, 2024
The
interaction
of
the
SARS-CoV-2
spike
protein
with
membrane-bound
angiotensin-converting
enzyme-2
(ACE-2)
receptors
in
epithelial
cells
facilitates
viral
entry
into
human
cells.
Despite
this,
ACE-2
exerts
significant
protective
effects
against
coronaviruses
by
neutralizing
viruses
circulation
and
mitigating
inflammation.
While
reduces
expression,
vitamin
D
increases
it,
counteracting
virus's
harmful
effects.
Vitamin
D's
beneficial
actions
are
mediated
through
complex
molecular
mechanisms
involving
innate
adaptive
immune
systems.
Meanwhile,
status
[25(OH)D
concentration]
is
inversely
correlated
severity,
complications,
mortality
rates
from
COVID-19.
This
study
explores
which
inhibits
replication,
including
suppression
transcription
enzymes,
reduced
inflammation
oxidative
stress,
increased
expression
antibodies
antimicrobial
peptides.
Both
hypovitaminosis
elevate
renin
levels,
rate-limiting
step
renin-angiotensin-aldosterone
system
(RAS);
it
ACE-1
but
expression.
imbalance
leads
to
elevated
levels
pro-inflammatory,
pro-coagulatory,
vasoconstricting
peptide
angiotensin-II
(Ang-II),
leading
widespread
It
also
causes
membrane
permeability,
allowing
fluid
infiltrate
soft
tissues,
lungs,
vascular
system.
In
contrast,
sufficient
suppress
reducing
RAS
activity,
lowering
ACE-1,
increasing
levels.
cleaves
Ang-II
generate
Ang
Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(5), P. 1277 - 1277
Published: April 25, 2023
Vitamin
D
and
its
role
in
the
coronavirus-19
disease
(COVID-19)
pandemic
has
been
controversially
discussed,
with
inconclusive
evidence
about
vitamin
D3
(cholecalciferol)
supplementation
COVID-19
patients.
metabolites
play
an
important
initiation
of
immune
response
can
be
easily
modifiable
risk
factor
25-hydroxyvitamin
(25(OH)D3)-deficient
This
is
a
multicenter,
randomized,
placebo-controlled
double-blind
trial
to
compare
effect
single
high
dose
followed
by
treatment
as
usual
(TAU)
daily
until
discharge
versus
placebo
plus
TAU
hospitalized
patients
25(OH)D3-deficiency
on
length
hospital
stay.
We
included
40
per
group
did
not
observe
significant
difference
median
stay
(6
days
both
groups,
p
=
0.920).
adjusted
for
factors
(β
0.44;
95%
CI:
-2.17-2.22),
center
0.74;
-1.25-2.73).
The
subgroup
analysis
severe
(<25
nmol/L)
showed
non-significant
reduction
intervention
(5.5
vs.
9
days,
0.299).
competing
model
death
reveal
differences
between
(HR
0.96,
CI
0.62-1.48,
0.850).
Serum
25(OH)D3
level
increased
significantly
(mean
change
nmol/L;
intervention:
+26.35
control:
-2.73,
<
0.001).
140,000
IU
+
shorten
but
was
effective
safe
elevation
serum
levels.
Healthcare,
Journal Year:
2022,
Volume and Issue:
10(5), P. 956 - 956
Published: May 22, 2022
Objectives:
Our
study
aimed
to
evaluate
the
usefulness
of
Vitamin
D3
(VitD3)
among
patients
hospitalized
for
COVID-19.
The
primary
endpoint
was
difference
in
survival
rates
between
receiving
and
not
VitD3.
secondary
endpoints
were
clinical
outcomes,
such
as
needing
non-invasive
ventilation
(NIV),
ICU
transfer,
laboratory
findings
(inflammatory
parameters).
Methods:
We
conducted
a
retrospective,
monocentric
matched-cohort
study,
including
attending
our
ward
Patients
divided
into
two
groups
depending
on
VitD3
administration
(Group
A)
or
B)
with
low
VitD
levels
(defined
blood
<
30
ng/mL),
which
depended
physicians’
judgment.
internal
protocol
provides
100,000
UI/daily
days.
Findings:
58
included
Group
A,
B.
matched
age,
sex,
comorbidities,
COVID-19-related
symptoms,
PaO2/FiO2
ratio,
exams,
medical
treatments.
Regarding
principal
endpoint,
there
statistically
significant
[Group
A
vs.
B
=
3
11
(p
0.042)].
When
considering
endpoints,
less
likely
undergo
NIV
12
23
0.026)]
showed
an
improvement
almost
all
inflammatory
parameters.
Conclusions:
link
deficiency
course
COVID-19
during
hospitalization
suggests
that
level
is
useful
prognostic
marker.
Considering
safety
supplementation
cost,
replacement
should
be
considered
SARS-CoV-2
infected
hospitalization.
Nutrients,
Journal Year:
2022,
Volume and Issue:
14(23), P. 5029 - 5029
Published: Nov. 26, 2022
Vitamin
C,
(ascorbic
acid),
vitamin
D
(cholecalciferol)
and
zinc
(zinc
sulfate
monohydrate)
supplements
are
important
in
immunity
against
coronavirus
disease-2019
(COVID-19).
However,
a
limited
number
of
studies
have
been
conducted
on
the
association
vitamins
with
reduced
risks
COVID-19
infection.
This
study
aims
to
evaluate
as
treatment
options
reduce
severity
COVID-19.
Data
were
collected
from
962
participants
13
December
2020
4
February
2021.
The
presence
was
confirmed
by
qRT-PCR.
Chi-square
test
multivariate
regression
analyses
conducted.
ratio
uptake
C:vitamin
D:zinc
1:1:0.95.
Uptake
significantly
associated
risk
infection
(OR:
0.006
(95%
CI:
0.03–0.11)
(p
=
0.004))
0.03
0.01–0.22)
0.005)).
tendency
taking
0.001),
age
0.02),
sex
0.05)
residence
0.04).
duration
supplementation
medication
hospitalization
0.0001).
Vitamins
not
0.9)
when
taken
through
diet.
Hospitalization
0.000001)
access
health
facilities
0.0097)
survival
period
participants.
Participants
better
recovered
early
6.21,
95%
CI
1.56–24.7).
will
add
knowledge
field
using
supplements.