Hair Longevity—Evidence for a Multifactorial Holistic Approach to Managing Hair Aging Changes
Gillian E. Westgate,
No information about this author
Daniela Grohmann,
No information about this author
Manuel Sáez Moya
No information about this author
et al.
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(6), P. 1894 - 1894
Published: March 11, 2025
Loss
of
hair
density—hair
thinning
and
balding—
is
typically
referred
to
as
male
female
pattern
alopecia.
Causes
include
genetic
predisposition
links
the
impact
dihydrotestosterone
on
follicle
dermal
papilla,
which
are
characterized
by
an
increase
in
number
vellus
follicles.
Links
chronological
aging
unclear.
Proven
treatments
remain
few
still
targeting
tested
those
experiencing
classical
loss.
The
way
changes
with
aging,
especially
women,
can
be
considered
having
a
much
broader
scope.
Trends
managing
density,
length,
fiber
quality
now
mostly
cocktail
approaches—whether
topical,
injected,
or
oral—recognizing
that
solutions
more
likely
require
multifactorial
strategy.
This
review
examines
evidence
for
holistic
approach
addressing
unwanted
loss,
includes
nutrition,
lifestyle,
stress
management,
scalp
care,
well
co-morbidities
other
health
concerns.
We
discuss
strengths
limitations
clinical
study
design
investigate
efficacy
using
approaches.
propose
this
strategy
will
contribute
emerging
concept
longevity
follicle,
scalp,
targeted
maintaining
anagen
most
appropriate
route
achieving
healthy
aging.
Finally,
we
problem
facing
patients
consumers
regarding
quantity
misinformation
how
it
influences
choosing
from
fast-growing
market
bypass
pharmaceutical
thinning.
Language: Английский
Evaluation of morphological and cytotoxic effects of minoxidil on Phaseolus vulgaris L. as a plant model
Environmental Science and Pollution Research,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 16, 2024
Language: Английский
Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
Cosmetics,
Journal Year:
2024,
Volume and Issue:
11(5), P. 148 - 148
Published: Aug. 27, 2024
Androgenetic
alopecia
(AGA)
is
the
most
common
form
of
hair
loss,
significantly
affecting
both
men
and
women
worldwide.
Characterized
by
progressive
thinning
AGA
primarily
mediated
dihydrotestosterone
(DHT).
Recent
research
has
identified
numerous
single-nucleotide
polymorphisms
(SNPs)
associated
with
AGA,
particularly
in
genes
involved
androgen
metabolism,
prostaglandin
pathways,
vasodilation.
These
genetic
markers
offer
insights
into
pathophysiology
potential
therapeutic
targets.
Pharmacogenetics,
study
how
variations
influence
drug
response,
holds
promise
for
personalized
treatment.
Identifying
SNPs
that
affect
efficacy
treatments
like
minoxidil
finasteride
enables
development
tailored
strategies.
For
instance,
variants
SRD5A2
gene,
which
affects
DHT
can
predict
responsiveness
to
5-alpha-reductase
inhibitors.
Beyond
pharmacogenetics,
RNA
interference
(RNAi)
technologies,
e.g.,
small
interfering
RNAs
(siRNAs),
present
new
avenues.
Studies
have
shown
RNAi-based
targeting
receptors,
promoting
growth
models.
Integrating
pharmacogenetic
clinical
practice
transform
management,
enhancing
treatment
patient
outcomes.
In
conclusion,
are
crucial
developing
while
emerging
RNAi
technologies
promising
interventions.
advancements
represent
significant
steps
toward
more
effective
individualized
therapies.
Language: Английский
Sublingual Minoxidil 5 mg versus Oral Minoxidil 5 mg for male androgenetic alopecia: A double‐blind randomized clinical trial
Journal of the European Academy of Dermatology and Venereology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 17, 2024
Low-dose
oral
minoxidil
(OM)
is
effective
for
male
androgenetic
alopecia
(AGA).1,
2
Sublingual
(SM)
was
proposed
as
an
alternative
to
minimize
adverse
systemic
cardiovascular
effects
and
increase
clinical
response
by
bypassing
the
hepatic
first-pass
metabolism
improving
bioavailability.3
Bypassing
would
reduce
rate
of
rise
circulating
activated
drug
its
vascular
effect.
However,
efficacy
tolerability
have
yet
be
compared
OM.4
This
double-blind,
randomized
trial
compares
efficacy,
safety
SM
5
mg
per
day
versus
OM
daily
24
weeks
in
patients
with
AGA.
Men
AGA
(Norwood-Hamilton
3
V,
4
V
V)
were
(1:1)
into
two
groups:
placebo
once
a
or
sublingual
weeks.
The
primary
outcome
change
total
hair
density
vertex
region
(TrichoLab®
H2H-matching
technology).5
Secondary
outcomes
included
changes
non-vellus
photographic
evaluations.
One
hundred
ten
participants
enrolled
specialized
clinic
Brazil
(Table
1).
Eighty-five
completed
study;
43
SL
group,
42
group.
increased
24.5
hairs/cm2
(95%
CI:
18.8–30.2)
group
21.8
14.9–29.0)
Non-vellus
7.8
4.2–11.4)
7.4
(95%CI:
mean
from
baseline
greater
but
this
difference
not
statistically
significant
(p
>
0.5).
According
consensus
three
treatment-blind
dermatologists,
42%
40%
showed
improvement
vertex,
no
between
groups
=
0.69)
2).
Hypertrichosis
main
event
reported.
Palpitation
less
frequent
(0%
vs.
9%;
p
0.048).
Minoxidil
pro-drug,
order
act,
it
must
bio-activated
sulfate.6
Considerable
inter-individual
variation
both
follicular
sulfotransferase
activity
may
explain
among
patients.7-9
In
previous
40
AGA,
proven
safe
at
doses
0.45,
1.35
4.05
day.4
No
described.
study,
different
administration
methods
did
impact
improvement.
there
frequency
palpitations.
vasodilation
caused
can
lead
reflex
tachycardia,
commonly
reported
few
hours
after
ingestion.
using
low-dose
(0.25–5
daily)
loss,
palpitations
been
described
up
4%
cases.10
absence
could
explained
escaping
immediate
liver
activation.
Maybe
other
events
like
hypertrichosis,
oedema
dizziness
because
they
depend
on
drug's
long-term
So,
impacted
short
differences.
limitations
our
study
include
single-centre
design,
blood
pressure
heart
monitoring,
small
sample
size.
conclusion,
demonstrate
superiority
over
treatment
Both
treatments
well
tolerated,
palpitation
principal
investigator
had
full
access
all
data
takes
responsibility
integrity
accuracy
analysis.
None.
BS,
CC,
PMR
HAM:
RS:
patents:
loss
(telogen
effluvium);
treat
excessive
shedding;
US10226462,
us16344288,
us201990269684,
us162522107;
Stock
owner:
Samson
Clinical
Pty
Ltd.
protocol
approved
Ethics
Committee
Anhaguera—UNIDERP
(#
5.936.863).
Consent
publication
recognizable
patient
photographs
identifiable
material
obtained
authors
time
article
submission
journal,
stating
that
gave
consent
understanding
information
publicly
available.
RBR-7wsgdm8.
support
findings
are
available
corresponding
author
upon
reasonable
request.
Language: Английский