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Year : 2014  |  Volume : 7  |  Issue : 4  |  Page : 213-219
Study of platelet-rich plasma injections in the treatment of androgenetic alopecia through an one-year period

1 Department of Dermatology and Venereology, Medical School, Democritus University of Thrace, Alexandroupolis, Greece
2 Laboratory of Medical Statistics, Democritus University of Thrace, Alexandroupolis, Greece
3 Department of Dermatology and Venereology, Medical School, Attikon Hospital, University of Athens, Athens, Greece

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Date of Web Publication4-Feb-2015


Background: Platelet-rich plasma (PRP) is defined as an autologous concentration of plasma with a greater count of platelets than that of whole blood. Its action depends on the released growth factors from platelets. It has been investigated and used in numerous fields of medicine. Recently, PRP has received growing attention as a potential therapeutic tool for hair loss. Aims: To evaluate the efficacy and safety of PRP injections in the scalp of patients with androgenetic alopecia. Settings and Design: Prospective cohort study. Materials and Methods: 20 patients, 18 males and 2 females, with androgenetic alopecia were enrolled in the study. PRP was prepared using a single spin method (Regenlab SA). Upon activation, it was injected in the androgen-related areas of scalp. Three treatment sessions were performed with an interval of 21 days and a booster session at 6 months following the onset of therapy. Statistical Analysis: Statistical analysis of the data was performed using the Statistical Package for the Social Sciences (SPSS), version 19.0 (IBM, NY, USA). Results: Hair loss reduced and at 3 months it reached normal levels. Hair density reached a peak at 3 months (170.70 ± 37.81, P < 0.001). At 6 months and at 1 year, it was significantly increased, 156.25 ± 37.75 (P < 0.001) and 153.70 ± 39.92 (P < 0.001) respectively, comparing to baseline. Patients were satisfied with a mean result rating of 7.1 on a scale of 1-10. No remarkable adverse effects were noted. Conclusions: Our data suggest that PRP injections may have a positive therapeutic effect on male and female pattern hair loss without remarkable major side effects. Further studies are needed to confirm its efficacy.

Keywords: Androgenetic alopecia, hair loss, platelet-rich plasma

How to cite this article:
Gkini MA, Kouskoukis AE, Tripsianis G, Rigopoulos D, Kouskoukis K. Study of platelet-rich plasma injections in the treatment of androgenetic alopecia through an one-year period. J Cutan Aesthet Surg 2014;7:213-9

How to cite this URL:
Gkini MA, Kouskoukis AE, Tripsianis G, Rigopoulos D, Kouskoukis K. Study of platelet-rich plasma injections in the treatment of androgenetic alopecia through an one-year period. J Cutan Aesthet Surg [serial online] 2014 [cited 2022 Jun 24];7:213-9. Available from:

   Introduction Top

Androgenetic alopecia (AGA) is a common chronic hair loss disorder. It is characterised by progressive hair loss, affecting both sexes. It affects up to 80% Caucasian men and 40% women. Its frequency increases with age, despite the fact that it may start at puberty. [1],[2] Independent of age and gender, patients diagnosed with AGA may undergo significant impairment of quality of life, since hair is considered to be an important feature of self-image. [3] Hair loss affects self-esteem, personal attractiveness and may lead even to depression and other negative effects of life, especially in women. [2],[3],[4]

A number of products have been proposed as hair loss therapies. Drug therapies specifically approved by Food and Drug Administration (FDA) for treating AGA are limited to minoxidil and finasteride. Both can be used alone or combined. [5] Despite the therapeutic options available, low patient compliance and satisfaction rate as well as the plethora of topical and often important systematic adverse effects lead to the search of new treatment options for AGA. [1],[5]

PRP is defined as a volume of the plasma fraction of autologous blood with an above baseline platelet concentration. [6] The regenerative potential of PRP depends on the levels of growth factors released upon activation. [7],[8] Main growth factors (GFs) involved in androgenetic alopecia are platelet-derived growth factor (PDGF), transforming growth factor (TGF),vascular endothelial growth factor (VEGF) and insulin-like growth factor (IGF) with their isoforms. [9],[10],[11],[12] GFs appear to act in the bulge area of the follicle, where they bind to their respective receptors located in stem cells. In the bulge area, primitive stem cells of ectodermal origin are found, giving origin to epidermal cells and sebaceous glands. In matrix, germinative cells of mesenchymal origin are found at the dermal papilla (DP). Interactions between these two kind of cells as well as with binding growth factors (PDGF, TGF-b and VΕGF) activate the proliferative phase of the hair, giving rise to the future follicular unit.[13] Therefore, PRP could serve as a potential treatment of AGA.

Aim of our study was to investigate the clinical efficacy and safety of PRP injections in the scalp of patients with AGA.

   Materials and Methods Top

From October 2012 to September 2013, 22 volunteers (20 men, 2 women) enrolled our study. All participants were ≥18, who had not received any topical or systematic treatment for their hair loss during the last 6 months. Patients with present or a history of immunosuppression (malignancy, chemotherapy, steroid therapy), dermatological diseases affecting the scalp, autoimmune disorders, hematologic disorders, platelet dysfunction syndrome and on anticoagulation therapy were excluded from our study. Patients with a tendency for keloids were also excluded. Patients taking aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs) discontinued their use 7 days before treatment.

Diagnosis of AGA was made in all patients based on a detailed medical history (any drugs causing hair loss), clinical examination and laboratory tests. Laboratory tests included:

  1. CBC;
  2. Serum iron, serum ferritin, TIBC (Total Iron-Binding capacity);
  3. Folic acid;
  4. T3, T4, TSH, fT3, fT4, anti-TPO;
  5. VDRL and
  6. For women, female hormone profile (DHEAS, testosterone, and rostenedione, prolactin, follicle stimulating and leutinising hormone).

Laboratory tests were assessed in order to exclude other hair loss causes, such as anaemia, poor nutrition, thyroid dysfunction, syphilis or polycystic ovary syndrome.

The stage of alopecia was evaluated according to the Hamilton-Norwood scale for men and Ludwig scale for women.

For the preparation of PRP, RegenKit BCT-3 (Regenlab ® ) was used. Initially, whole blood was collected from the antecubital vein of the patient (16 ml). The blood was then introduced into two tubes (RegenBCT) and centrifugated for 5 min at 1500 g using the laboratory centrifuge RegenA-PRPCentri. Each tube contained a thixotropic gel composed of a mixture of polymers for plasma separation (elimination of red blood cells) and sodium citrate solution, as an anticoagulant, located above the separator gel. Therefore, after centrifugation, the blood was fractionated with the red blood cells being trapped under the gel and cellular elements settling on the surface of the gel. After removal of 2 ml of upper supernatant plasma (PPP, platelet-poor plasma) from each tube, 3 ml of PRP was yielded, which was resuspended by gentle inversions of the tube. Total amount of yielded PRP was about 6 ml and it was loaded in 1 ml syringes, ready for injections. The activation process included the addition of calcium gluconate in a 1:9 ratio (0.1 ml calcium gluconate per 0.9 ml of PRP). The platelets in whole blood and PRP were microscopically counted and mean platelet counts were 1.9 × 10 5 and 1.102 × 10 6 platelets/μl, respectively. The concentration of platelets in PRP was approximately 5.8 times as great as that in whole blood.

Before the PRP applications, all patients were informed about the process and its potent adverse effects and they signed a consent form. They did not have their hair washed two days prior to the treatment. Local anaesthesia was applied in the treatment area and scalp was cleaned using 0.1% octenidine hydrochloride spray. None of the patients received any other treatment for hair loss during PRP treatment.

PRP (0,05-0,1 ml/cm 2 ) was injected, with a 27-G needle, into the androgen-related areas (frontal, parietal, occipital) of the scalp in men and into the problematic areas in women, using BD-Luer LokTM 1 ml syringes. Nappage technique was performed in a depth of 1.5-2.5 mm [Figure 1]. Our protocol proposed three treatment sessions with an interval of 3 weeks. At 6 months from the beginning of the treatment, a booster session was also performed.
Figure 1: Injecting activated PRP

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In our study, we evaluated hair loss, hair density (hair/cm 2 ) and patients' satisfaction. We also noted any reported adverse effects. The evaluation of results was performed by two independent evaluators, who were not involved in the administration of PRP treatment. Evaluation methods included hair pull test, dermoscopic photomicrographs, macroscopic photographs and a satisfaction questionnaire. All patients were evaluated at six time points: T1, beginning of study; T2, 3 weeks; T3, 6 weeks; T4, 3 months; T5, 6 months; and T6, 1 year.

In order to check the same area at all time points, we used 'V' (Kang's point), as proposed by Lee et al. [14] 'V' is the point of intersection between the midsagittal line and the coronal line connecting the tips of the tragus. By using a plastic headband and a tapeline, 'V' can be measured conveniently because the headband presents the coronal line connecting the roots of the ear vagus, and the tapeline easily shows the midsagittal line [Figure 2]. We measured 'V', which is located roughly 1 to 1.3 cm in front of the anterior margin of the headband and record the distance from the headband to the midpoint of the line connecting the lower margins of the eyebrows for reproducibility.
Figure 2: Defining V point using a headband and a tapeline

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Statistical analysis of the data was performed using the Statistical Package for the Social Sciences (SPSS), version 19.0 (IBM, NY, USA). The normality of quantitative variables was tests by Kolmogorov-Smirnov test. Hair density was expressed as mean ± standard deviation (SD). Hair density differences between the different time points were assessed by one-way repeated measures ANOVA (rmANOVA); post hoc analysis was performed using the Sidak test. All tests were two tailed and statistical significance was considered for P values less than 0.05.

   Results Top

A total of 22 patients enrolled in the study. Nevertheless, there was a dropout of two patients, who did not complete the therapy protocol and were not included in the statistical analysis. Therefore, 20 patients (18 men, 2 women) were finally included in the study. In [Table 1], a summary of patients' characteristics is presented. The mean age of patients was 34 years (24-72). Among men, according to the Hamilton-Norwood scale, five patients suffered from type II androgenetic alopecia, eight from type III, four from type IV and one from type V alopecia. Both women suffered from I-3 androgenetic alopecia, according to the Ludwig scale. Six patients had previously soughtb medical help for their hair loss and they had been treated with topical minoxidil lotion 5%. During the last 6 months since the onset of PRP therapy, they had not received any medication. None had undergone hair transplantation. Two male patients had been taking NSAIDs due to musculoskeletal problems and they stopped those 8 days before PRP injections.
Table 1: Patients' characteristics

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In [Figure 3], we present the number of hairs taken at the hair pull test. It was performed in a standardised manner by the two evaluators. Despite the fact that it is not an objective evaluation method, it gives a satisfactory general image of hair loss. At T1, the mean number of hairs pulled was eight while at T3 and at T4 reached normal levels, since less than three hairs pulled are considered to constitute normal hair loss. At T5 and at T6, the mean hair loss increased with a number of five and six hairs respectively pulled during hair pull test.
Figure 3: Number of hairs pulled during hair pull test

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Hair density (hair/cm 2 ) significantly increased at T3 (154.80 ± 34.39), at T4 (170.70 ± 37.81) at T5 (156.23 ± 37.75) and at T6 (153.70 ± 39.92) (P < 0.001) compared to the onset of therapy (T1). The highest hair density recorded was at T4 [Table 2], [Figure 4]. The % increase rate from baseline (T1) was 0.45%, 8.18%, 19.9%, 9.19% and 7.41% at T2, T3, T4, T5 and at T6, respectively. Regarding failure rate, at T3 and T4, none of the patients presented decreased hair density compared to that of baseline and only one of them presented no change (5%). At T5, one patient (5%) presented a decrease of 1 hair/cm 2 in hair density comparing to that of T1, while at T6 30% presented a mean decrease of 2 hair/cm 2 .
Figure 4: The effect of activated platelet-rich plasma injections on hair density through a 1-year period. Statistical significance is considered for P values less than 0.05

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Table 2: Hair density (mean ± SD) in different time points

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Macroscopic photographs showed an overall improvement in hair density and quality, as laguno-like hair became thicker, normal hair [Figure 5], [Figure 6], [Figure 7] and [Figure 8].
Figure 5: Male, 29-year-old, before treatment

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Figure 6: The same patient at 6 months following the onset of PRP treatment

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Figure 7: Male, 26 years old, before treatment

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Figure 8: The same patient at three months after treatment

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Patients filled in the patients' satisfaction questionnaire and reported any adverse effects. They were satisfied with a mean result rating of 7.1 on a linear analogue scale of 1-10 (1 = no result, 10 = best result). 85% of patients reported an improvement in hair quality and thickness flash»), while 65% reported an increase in hair density. At T5, all patients (100%) claimed that they want and/or need the booster session, while, at T6, 75% of needed them.

Regarding PRP›s safety profile, in the satisfaction questionnaire patients reported any adverse effects. During application, 100% of them felt mild pain, despite local anaesthesia. After application, 25% of them felt a mild pain feeling, which subsided after 4 hours, while 60% had scalp sensitivity during first hair wash after treatment injections. None reported any worsened hair shedding, infection or ecchymosis.

   Discussion Top

AGA remains the most common hair disorder without satisfactory treatment. Since androgenetic alopecia is characterised by a shortened anagen phase and miniaturisation of terminal to vellus hair, [5] current therapeutic strategies target cellular proliferation and differentiation during the hair cycle.

Except scalp surgery, which is a surgical treatment option, FDA-approved drug therapies include finasteride and minoxidil. [1],[5],[15] Minoxidil appears to prolong anagen phase and to promote survival of dermal papilla cells and increase in hair follicle size. [16],[17] Finasteride also promotes hair growth of anagen hairs leading to gradual increase in hair diameter and hair elongation [18] and appears to activate anagen hair growth. [19],[20]

Presently, there are limited published data regarding PRP's potential effect on hair. Activated PRP seems to promote differentiation of stem cells into hair follicle cells through the upregulation of transcriptional activity of β-catenin. It also induces in vitro proliferation of dermal papilla cells, and increases dermal papilla cell growth by activating ERK signalling. PRP also appears to prolong anagen phase of hair growth cycle through increased expression of FGF-7 and to increase cell survival by inhibiting apoptosis (associated with increased Bcl-2 protein levels as well as activated Akt signalling). [21] It also appears to increase the perifollicular vascular plexus, through the increase of VEGF and PDGF levels, which have an angiogenic potential. Therefore, it constitutes a potent useful tool for androgenetic alopecia treatment. [12]

In our study using non-invasive evaluation methods, such as dermoscopic photomicrographs, [Figure 9] and [Figure 10] a significant increase rate in hair density of 19,29% and 9,19% was noted at 3 and 6 months respectively with large variability in results (from no improvement to significant improvement). Hair density followed an upward curve, reached a peak at 3 months, decreased at 6 months but its value was significant higher than that of baseline (T1). At 1 year (T6), hair density continued its downward trend although remaining significantly higher than that of T1. Hair loss after the second treatment session (T3) decreased and at T4 reached normal levels. Nevertheless, at 6 months (T5), number of hairs pulled during hair pull test were increased to five, without, however, reaching the number of eight hairs of T1. Taking these in account, the booster session at 6 months was necessary, in order to maintain and improve the results achieved. Finally, at 1 year (T6), number of hairs pulled increased to six, less than eight (T1).
Figure 9: Dermoscopic photomicrographs from a male, 32-year-old, with grade III androgenetic alopecia, before the onset of treatment (x10 magnification)

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Figure 10: Dermoscopic photomicrographs, from the same 32-year-old patient, at 3 months following treatment (x10 magnification)

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Patients with grade II-III alopecia according to the Norwood-Hamilton scale had better results compared to patients with more advanced alopecia. Both women were satisfied with the results. Furthermore, patients with vellus hair had better results compared to those who had few but normal hair, as PRP appeared to act on hair diameter causing thin hair to become thicker.

Advantage of our study was that we used a standardised approved PRP preparation kit (Regenkit-BCT-3), since automated kits appear to give better results as mentioned in the literature. Furthermore, we described in detail our protocol of PRP preparation and application, making our results reproducible. Our follow-up, also, was longer (1 year) compared to most other studies.

Nevertheless, our study was not a randomised, double-blind, controlled trial and potent bias might be present. In our case, for instance, most of our patients had vellus hair and were non-smokers. Smoking is mentioned since PRP promotes and improves hair follicle vascularisation. Therefore, smoking as well as other factors affecting microcirculation may play a role in trial results.

Apart from these, hair evaluation methods were not objective. Hair pull test was performed in a standardised manner by the two evaluators, but it remains a subjective evaluation method. Macroscopic photographs showed an overall image of hair growth and hair density. Dermoscopic photomicrographs showed an increase in hair density as number of hairs were counted manually by the evaluators twice and was the most objective method. Phototrichogram, a more objective evaluation method was not performed as it needs to be performed on a shaven part of the patient's scalp which is not accepted by most patients, particularly women. Nevertheless, an adequate means of measuring hair growth over time in a reproducible, economical and non-invasive manner is not available and all the above methods give a relatively fair assessment of the results after treatment.

Finally, sample size was small, despite the fact that we had statistical significant results.

   Conclusion Top

In conclusion, PRP injections appeared to be effective in the treatment of androgenetic alopecia in both males and females, without remarkable adverse effects, while they were accompanied by a high patients' satisfaction rate. Nevertheless, more randomised, controlled, double-blind studies with approved devices for PRP preparation, details in PRP preparation and application, with larger sample size, longer follow-up and objective evaluation methods are needed. The questions are whether PRP will provide as much benefit as existing treatment options, such as minoxidil and whether it could be used as monotherapy or in combination with other treatments. Nevertheless, it seems to be a good choice especially for women of childbearing age, who cannot take oral medication such as finasteride, and for patients with adverse effects and/or no results from finasteride or minoxidil.

   References Top

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Cash TF, Price VH, Savin RC. Psychological effects of androgenetic alopecia on women: Comparisons with balding men and with female control subjects. J Am Acad Dermatol 1993;29:568-75.  Back to cited text no. 4
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Correspondence Address:
Dr. Maria-Angeliki Gkini
6th km Alexandroupolis-Makris, 68100, Alexandroupolis
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0974-2077.150743

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  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10]

  [Table 1], [Table 2]

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23 Comparison between single- versus double-spin prepared platelet-rich plasma injection in treatment of female pattern hair loss: clinical effect and relation to vascular endothelial growth factor
Rania Mahmoud El-Husseiny, Haitham M. Saleh, Afaf A. Moustafa, Samar A. Salem
Archives of Dermatological Research. 2021; 313(7): 557
[Pubmed] | [DOI]
24 Successful Treatment of Corticosteroid-Induced Rosacea-Like Dermatitis with Platelet-Rich Plasma Mesotherapy: Report of Seven Cases
Xing Fan, Yue Yin, Wenjie Dou, Tong Li, Ping Xue, Qing Yang, Qiaoxin Ma
Dermatology and Therapy. 2021; 11(2): 615
[Pubmed] | [DOI]
25 Effects of Intraovarian Injection of Autologous Platelet-Rich Plasma on Ovarian Rejuvenation in Poor Responders and Women with Primary Ovarian Insufficiency
Abbas Aflatoonian, Marzieh Lotfi, Lida Saeed, Nasim Tabibnejad
Reproductive Sciences. 2021; 28(7): 2050
[Pubmed] | [DOI]
26 Platelet-rich Plasma and Cell Therapy
Aditya K. Gupta, Helen J. Renaud, Jeffrey A. Rapaport
Dermatologic Clinics. 2021; 39(3): 429
[Pubmed] | [DOI]
27 Physiology and Medical Treatments for Alopecia
Tymon Tai, Amit Kochhar
Facial Plastic Surgery Clinics of North America. 2020; 28(2): 149
[Pubmed] | [DOI]
28 Platelet-Rich Plasma for Hair Restoration
Natalie Justicz, Adeeb Derakhshan, Jenny X. Chen, Linda N. Lee
Facial Plastic Surgery Clinics of North America. 2020; 28(2): 181
[Pubmed] | [DOI]
29 Evaluation of platelet-rich plasma as a treatment for androgenetic alopecia: A randomized controlled trial
Jerry Shapiro, Anthony Ho, Kumar Sukhdeo, Lu Yin, Kristen Lo Sicco
Journal of the American Academy of Dermatology. 2020; 83(5): 1298
[Pubmed] | [DOI]
30 Platelet-Rich Plasma in the Treatment of Alopecia Areata: A Review
Hind M. Almohanna, Azhar A. Ahmed, Jacob W. Griggs, Antonella Tosti
Journal of Investigative Dermatology Symposium Proceedings. 2020; 20(1): S45
[Pubmed] | [DOI]
31 A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review
Sumel Ashique, Navjot Kaur Sandhu, Sk. Niyamul Haque, Kartick Koley
Natural Products and Bioprospecting. 2020; 10(6): 345
[Pubmed] | [DOI]
32 Platelet-Rich Plasma and its Use for Cicatricial and Non-Cicatricial Alopecias: A Narrative Review
Rubina Alves, Ramon Grimalt
Dermatology and Therapy. 2020; 10(4): 623
[Pubmed] | [DOI]
33 The Physician's Guide to Platelet-Rich Plasma in Dermatologic Surgery Part I: Definitions, Mechanisms of Action, and Technical Specifications
Amelia K. Hausauer, Shannon Humphrey
Dermatologic Surgery. 2020; 46(3): 348
[Pubmed] | [DOI]
34 The Physician's Guide to Platelet-Rich Plasma in Dermatologic Surgery Part II: Clinical Evidence
Amelia K. Hausauer, Shannon Humphrey
Dermatologic Surgery. 2020; 46(4): 447
[Pubmed] | [DOI]
35 A Randomized, Controlled Pilot Trial Comparing Platelet-Rich Plasma to Topical Minoxidil Foam for Treatment of Androgenic Alopecia in Women
Alison J. Bruce, Thais P. Pincelli, Michael G. Heckman, Cheryl M. Desmond, Jennifer R. Arthurs, Nancy N. Diehl, Erika J. Douglass, Charles J. Bruce, Shane A. Shapiro
Dermatologic Surgery. 2020; 46(6): 826
[Pubmed] | [DOI]
36 Platelet-rich plasma as a therapy for androgenic alopecia: a systematic review and meta-analysis
Adam G. Evans, James M. Mwangi, Rand W. Pope, Mirjana G. Ivanic, Mina A. Botros, Gabriella E. Glassman, F. Bennett Pearce, Salam Kassis
Journal of Dermatological Treatment. 2020; : 1
[Pubmed] | [DOI]
37 Evaluation of the effect of autologous platelet-rich plasma on androgenic alopecia
Mahmoud Makki, Abdel-Khalek Hassan Younes, Islam Salah
Journal of Cosmetic and Laser Therapy. 2020; 22(4-5): 190
[Pubmed] | [DOI]
38 Growth factor concentrations in platelet-rich plasma for androgenetic alopecia: An intra-subject, randomized, blinded, placebo-controlled, pilot study
Tee Wei Siah, Hongwei Guo, Thomas Chu, Leopoldo Santos, Hisae Nakamura, Gigi Leung, Jerry Shapiro, Kevin J. McElwee
Experimental Dermatology. 2020; 29(3): 334
[Pubmed] | [DOI]
39 Platelet-rich plasma associated with hair transplants for the treatment of androgenetic alopecia showed no benefits
C. Graf Guimarães, F. Mulinari-Brenner, B. Werner, S. Kusma
Journal of the European Academy of Dermatology and Venereology. 2020; 34(7)
[Pubmed] | [DOI]
40 QR 678 & QR678 Neo Vs PRP—A randomised, comparative, prospective study
Rinky Kapoor, Debraj Shome, Sapna Vadera, M. Shiva Ram
Journal of Cosmetic Dermatology. 2020; 19(11): 2877
[Pubmed] | [DOI]
41 Review of the Use of Platelet-Rich Plasma in the Treatment of Alopecia
Emma Coleman
Plastic Surgical Nursing. 2020; 40(2): 68
[Pubmed] | [DOI]
42 Platelet-rich plasma for androgenetic alopecia: Efficacy differences between men and women
Aditya K. Gupta, Helen J. Renaud, Mary Bamimore
Dermatologic Therapy. 2020; 33(6)
[Pubmed] | [DOI]
43 Platelet Rich Plasma in Androgenetic Alopecia- A Prospective Study
Mary Vineetha, Seena Palakkal, Jaya K. V.
Journal of Evolution of Medical and Dental Sciences. 2020; 9(22): 1696
[Pubmed] | [DOI]
44 Treatment of Male-Pattern Alopecia with Platelet-Rich Plasma
Aline Lissa Okita, Denise Steiner, Sineida Berbert Ferreira, Paulo Müller Ramos, Walter Ferreira, Rebecca Silveira, Maria Luiza Mussi, Rafael Eliahu Vaidergorn, Rachel Berbert Ferreira
Skin Appendage Disorders. 2020; 6(2): 97
[Pubmed] | [DOI]
45 Using platelet-rich plasma to treat hair loss and thinning
Daniel Sister
Journal of Aesthetic Nursing. 2020; 9(10): 420
[Pubmed] | [DOI]
46 Using platelet-rich plasma to treat hair loss and thinning
Daniel Sister
Journal of Aesthetic Nursing. 2020; 9(8): 326
[Pubmed] | [DOI]
47 Bone regeneration in rabbit calvarial defects using PRGF and adipose-derived stem cells: histomorphometrical analysis
Arturas Stumbras, Povilas Kuliesius, Adas Darinskas, Ricardas Kubilius, Vilma Zigmantaite, Gintaras Juodzbalys
Regenerative Medicine. 2020; 15(4): 1535
[Pubmed] | [DOI]
48 Androgenetic alopecia in women and men: Italian guidelines adapted from European Dermatology Forum/European Academy of Dermatology and Venereology guidelines
Aurora Alessandrini, Michela Starace, Roberto D'''''Ovidio, Lucia Villa, Alfredo Rossi, Teodora R. Stan, Piergiacomo Calzavara-Pinton, Bianca M. Piraccini
Giornale Italiano di Dermatologia e Venereologia. 2020; 155(5)
[Pubmed] | [DOI]
49 Therapeutic efficacy of TriCell CD34+ cell-containing, platelet-rich plasma in alopecia patients
Kyung Bong Kim, Dae Kwan Kim
Journal of Cosmetic Medicine. 2020; 4(1): 36
[Pubmed] | [DOI]
50 Systematic Review of Platelet-Rich Plasma Use in Androgenetic Alopecia Compared with Minoxidil®, Finasteride®, and Adult Stem Cell-Based Therapy
Pietro Gentile, Simone Garcovich
International Journal of Molecular Sciences. 2020; 21(8): 2702
[Pubmed] | [DOI]
51 Comparative Evaluation of the Clinical Efficacy of PRP-Therapy, Minoxidil, and Their Combination with Immunohistochemical Study of the Dynamics of Cell Proliferation in the Treatment of Men with Androgenetic Alopecia
Elena E. Pakhomova, Irina O. Smirnova
International Journal of Molecular Sciences. 2020; 21(18): 6516
[Pubmed] | [DOI]
52 Comparison of efficacy of platelet-rich plasma therapy with or without topical 5% minoxidil in male-type baldness: A randomized, double-blind placebo control trial
SatyendraKumar Singh, Vijay Kumar, Tulika Rai
Indian Journal of Dermatology, Venereology and Leprology. 2020; 86(2): 150
[Pubmed] | [DOI]
53 Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
Samuel H. Wood, E. Scott Sills
Clinical and Experimental Reproductive Medicine. 2020; 47(2): 94
[Pubmed] | [DOI]
54 Cyberspace Chat: Platelet Rich Plasma (PRP) and Its Use in Hair Restoration
Robin Unger
International Society of Hair Restoration Surgery. 2017; 27(3): 105
[Pubmed] | [DOI]
55 Injections of platelet-rich plasma for androgenic alopecia: A systematic review
F. Picard, B. Hersant, J. Niddam, J.-P. Meningaud
Journal of Stomatology, Oral and Maxillofacial Surgery. 2017; 118(5): 291
[Pubmed] | [DOI]
56 Using platelet-enriched autologous plasma for treatment of non-scarring alopecias (androgenetic and circumscribed alopecia)
A. N. Mareyeva, I. N. Kondrakhina, M. G. Abuladze
Vestnik dermatologii i venerologii. 2015; 91(3): 62
[Pubmed] | [DOI]
57 The Effect of Platelet-Rich Plasma in Hair Regrowth: A Randomized Placebo-Controlled Trial
Pietro Gentile, Simone Garcovich, Alessandra Bielli, Maria Giovanna Scioli, Augusto Orlandi, Valerio Cervelli
Stem Cells Translational Medicine. 2015; 4(11): 1317
[Pubmed] | [DOI]


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