Androgenetic Alopecia Clinical Trial
Official title:
Efficacy of Platelet-Rich Plasma Therapy for Androgenetic Alopecia: A Systematic Review and Meta-analysis
assess the literature on PRP outcomes for AGA, with a focus on specific clinical outcomes in a comparative view, in accordance with PRISMA statement for reporting this meta-analysis
Androgenic alopecia (AGA) also known as androgenetic alopecia or male pattern baldness, is a
common disorder that affects both men and women. Is one of the commonest reasons for
dermatological consultation worldwide (1). It is characterized by progressive hair loss,
especially of scalp hair, and has distinct patterns of loss in women versus men. AGA is an
age-dependent disorder characterized by patterned hair loss. Based on the few prevalence data
available, Know that by the age of 30 years about 30% of men will have AGA and that this will
rise to about 50% by the age of 50 years and as many as 90% in their lifetime (2) , Although
prevalence increases with age in all populations, thinning can begin as early as puberty (3).
The hair thinning begins between the ages of 12 and 40 years in both sexes and approximately
half the population expresses this trait to some degree before the age of 50 years (4).
Androgentic alopecia is familial with a complex polygenic mode of inheritance (5) .
Polymorphism of the androgen receptor gene, the 5 a reductase gene and 2 other, as yet
unidentified genes on chromosomes 3 and 21 have been all been associated with premature
balding (6). There is a family tendency towards androgenetic alopecia and it is thought to
have a polygenic mode of inheritance. Alopecia causes major discomfort due to altered
appearance with significant implications in daily living and possible leading to depression
and anxiety symptoms with a significantly higher prevalence in AGA female compared with male
subjects (7). Pathophysiology upon entry of testosterone into the hair follicle via dermal
papilla's capillaries, binding occurs to the androgen receptors (ARs) either directly or
after its conversion to dihydrotestosterone (DHT) (8). AGA is known to be mediated by the
conversion of circulating androgens into DHT within the hair follicle .In the hair follicle
cells, testosterone converts into the biologically more active metabolite; DHT, which is
considered the key androgen required for the induction of AGA (9). This conversion is
catalyzed by the enzyme 5α-reductase type-II. Binding of androgens to their ARs leads to
conformational change of the AR-androgen complex which is then transported into the nucleus
where it can bind to DNA which has distinctive binding sites: In most men, AGA involves the
fronto temporal area and the vertex, following a pattern corresponding to the Hamilton-
Norwood scale (10). In women, typically three patterns have been 1-Diffuse thinning of the
crown region with preservation of the frontal hairline 2-Thinning and widening of the central
part of the scalp with breach of frontal hairline, 3- Thinning associated with bitemporal
recession (Hamilton-Norwood type, diagnostic evaluation form for AGA, including history,
clinical evaluation like scalp and hair examination and diagnostic techniques and test (Pull
test, Wash test), and clinical documentation . AGA can be treated medically, surgically or
cosmetically (11) The most recommended treatment for AGA is composed of local minoxidil,
hormonal therapy such as local and oral antiandrogens (12).
Platelet-rich plasma (PRP) is used as an innovative therapy in diverse fields including
dentistry, surgery, orthopedics, dermatology and aesthetics (13). Currently, PRP preparation
systems have FDA clearance for use in bone grafts and operative Orthopedics but off-label
purposes such as for hair restoration have become increasingly common. PRP is a rich source
of growth factors such as insulin-like growth factor 1 (IGF-1), platelet-derived growth
factor (PDGF), transforming growth factor-b (TGF-b), vascular endothelial growth factor
(VEGF), epidermal growth factor (EGF) and fibroblast growth factor (FGF) which together can
stimulate cell survival, proliferation, differentiation, vascularization and angiogenesis
(14). Application of these growth factors to dermal papilla (DP) cells can lead to the
initiation and prolongation of anagen phase in the hair follicle. Alpha granules within the
platelets contain the growth factors and facilitate release at high concentrations, when the
PRP preparation is activated. PRP is produced through cell separation by commercial kits or
manual methods using a laboratory centrifuge and then injected into androgen-dependent areas
of the scalp ( 15). With more hair restoration clinics choosing to offer PRP therapy, data on
treatment efficacy have begun to accumulate. The AGA application remains in the early stages
as treatment protocols are still being refined. At this time, PRP has been used in
combination with hair transplant surgery and as an injectable therapy alone. Furthermore,
diverse methods are reported as activators can be used to stimulate growth factor release;
additional components such as leukocytes and dalteparin and protamine micro particles may be
included to boost results; and quantity and frequency of treatments have varied widely (16).
The conduction of a meta-analysis provides systematic assessment of previous research studies
to derive conclusions about that body of research. Outcomes from a meta-analysis may include
a more precise estimate of the effect of treatment than any individual study .
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