Short-Term Efficacy of Autologous Cellular Micrografts in Male and Female Androgenetic Alopecia: A Retrospective Cohort Study

Shadi Zari, Shadi Zari

Abstract

Purpose: Autologous cellular micrografts (ACM) is a novel treatment method in hair loss, and few data are available regarding its efficacy. The present study was carried out to assess the short-term clinical efficacy of a single application of ACM in the treatment of male and female androgenetic alopecia (AGA).

Materials and methods: This was a single-center retrospective study involving 140 consecutive adults with confirmed AGA, who received a single session of ACM (Regenera Activa®). Efficacy was evaluated 1-6 months after treatment, by analyzing the change of trichometry parameters, which were assessed using TrichoScan digital image analysis.

Results: Depending on the scalp region, there was increase in mean hair density by 4.5-7.12 hair/cm2, average hair thickness by 0.96-1.88 μm, % thick hair by 1.74-3.26%, and mean number of follicular units by 1.30-2.77, resulting in an increase of cumulative hair thickness by 0.48-0.56 unit. Additionally, the frontal region showed a significant decrease in % thin hair (-1.81%, p = 0.037) and yellow dots (-1.93 N/cm2, p = 0.003). A favorable response was observed in 66.4% of the participants in the frontal region. Further, a gender-specific effect of treatment was observed.

Conclusion: ACM is a promising treatment in AGA with a short-term favorable response observed in up to approximately two-thirds of patients.

Keywords: androgenetic alopecia; autologous cellular micrografts; efficacy; pattern hair loss; regrowth.

Conflict of interest statement

The author reports no conflicts of interest for this work and has no financial interests to disclose.

© 2021 Zari.

Figures

Figure 1
Figure 1
Area coverage index (ACI) definition, calculation formula and pixel transformation method. The figure describes the method proposed by the author to portray the visual aspect of the scalp as a function of the hair density and average hair thickness, by the (A) unit definition, (B) calculation and (C) pixel transformation of an area coverage index (ACI).
Figure 2
Figure 2
Change in key indicators of hair growth, by scalp region, in male and female androgenic alopecia after treatment with autologous cellular micrografts (ACM). Pictures depict: 1) relative pre- to post-intervention change (in percent, left panels) of the 5 positive (green bars) and 2 negative (Orange bars) parameters as adjusted by the respective baseline population mean, that is, bar heights represent the percentage of change in the given parameter by reference to the baseline population mean; 2) mean derived Sinclair grade (right panels) in baseline versus after treatment with ACM. Panels correspond to findings in different scalp regions including frontal (A), temporal (B), and occipital (C) regions.
Figure 3
Figure 3
Short-term hair growth in male and female androgenic alopecia after treatment with autologous cellular micrografts (ACM). Pictures depict pre- to post-intervention change in area coverage index (ACI) in the frontal (A), temporal (B), and occipital (C) regions. Each grid represents 9cm2 (3×3cm) of scalp area; where gray cells represent the scalp area covered by hair, white cells represent the scalp areas not covered by hair, and dark gray cells represent highly dense areas indicating ACI > 1cm2.
Figure 4
Figure 4
Pre and post treatment scalp photographs of a sample female and male patients with androgenetic alopecia, before and after treatment with autologous cellular micrografts (ACM). Photographs show cosmetic improvement after autologous cellular micrografts in a female (1) and a male (2) patient. In the female patient (1), there was increase in CHT from 10.3, 7.5 and 9.9 to 10.5, 8.3 and 12 mm/cm2 in frontal, temporal and occipital areas, respectively. In the male patient (2), there was increase in CHT from 12.7 to 13.2 mm/cm2 in the frontal and 8.8 to 12.3 mm/cm2 in the occipital area, while CHT decreased from 8.5 to 7.5 mm/cm2 in the temporal area.

References

    1. Bolduc C, Shapiro J. Management of androgenetic alopecia. Am J Clin Dermatol. 2000;1(3):151–158. doi:10.2165/00128071-200001030-00002
    1. Price VH. Treatment of hair loss. N Engl J Med. 1999;341(13):964–973.
    1. Bienenfeld A, Azarchi S, Lo Sicco K, Marchbein S, Shapiro J, Nagler AR. Androgens in women: androgen-mediated skin disease and patient evaluation. J Am Acad Dermatol. 2019;80(6):1497–1506. doi:10.1016/j.jaad.2018.08.062
    1. Villez RL. Topical minoxidil therapy in hereditary androgenetic alopecia. Arch Dermatol. 1985;121(2):197–202. doi:10.1001/archderm.1985.01660020055017
    1. Olsen EA, DeLong ER, Weiner MS. Dose-response study of topical minoxidil in male pattern baldness. J Am Acad Dermatol. 1986;15(1):30–37. doi:10.1016/S0190-9622(86)70138-2
    1. Katz HI. Topical minoxidil: review of efficacy. Clin Dermatol. 1988;6(4):195–199. doi:10.1016/0738-081X(88)90087-9
    1. Olsen EA, Whiting D, Bergfeld W, et al. A multicenter, randomized, placebo-controlled, double-blind clinical trial of a novel formulation of 5% minoxidil topical foam versus placebo in the treatment of androgenetic alopecia in men. J Am Acad Dermatol. 2007;57(5):767–774. doi:10.1016/j.jaad.2007.04.012
    1. Tsuboi R, Tanaka T, Nishikawa T, et al. A randomized, placebo-controlled trial of 1% topical minoxidil solution in the treatment of androgenetic alopecia in Japanese women. Eur J Dermatol. 2007;17(1):37–44.
    1. Blume-Peytavi U, Hillmann K, Dietz E, Canfield D, Garcia Bartels N. A randomized, single-blind trial of 5% minoxidil foam once daily versus 2% minoxidil solution twice daily in the treatment of androgenetic alopecia in women. J Am Acad Dermatol. 2011;65(6):1126.e2–1134.e2. doi:10.1016/j.jaad.2010.09.724
    1. Friedman ES, Friedman PM, Cohen DE, Washenik K. Allergic contact dermatitis to topical minoxidil solution: etiology and treatment. J Am Acad Dermatol. 2002;46(2):309–312. doi:10.1067/mjd.2002.119104
    1. Wilton L, Pearce G, Edet E, Freemantle S, Stephens MDB, Mann RD. The safety of finasteride used in benign prostatic hypertrophy: a non-interventional observational cohort study in 14,772 patients. Br J Urol. 1996;78(3):379–384. doi:10.1046/j.1464-410X.1996.00091.x
    1. Irwig MS, Kolukula S. Persistent sexual side effects of finasteride for male pattern hair loss. J Sex Med. 2011;8(6):1747–1753. doi:10.1111/j.1743-6109.2011.02255.x
    1. Ganzer CA, Jacobs AR, Iqbal F. Persistent sexual, emotional, and cognitive impairment post-finasteride: a survey of men reporting symptoms. Am J Men’s Health. 2015;9(3):222–228. doi:10.1177/1557988314538445
    1. Ekmekci TR, Sakiz D, Koslu A. Occipital involvement in female pattern hair loss: histopathological evidences. J Eur Acad Dermatol Venereol. 2010;24(3):299–301. doi:10.1111/j.1468-3083.2009.03411.x
    1. Birch MP, Lalla SC, Messenger AG. Female pattern hair loss. Clin Exp Dermatol. 2002;27(5):383–388. doi:10.1046/j.1365-2230.2002.01085.x
    1. Olsen EA. Androgenetic alopecia. In: Olsen EA, editor. Disorders of Hair Growth. McGraw-Hill; 1994:257–284.
    1. Owczarczyk-Saczonek A, Krajewska-Włodarczyk M, Kruszewska A, et al. Therapeutic potential of stem cells in follicle regeneration. Stem Cells Int. 2018;2018:1049641. doi:10.1155/2018/1049641
    1. Elmaadawi IH, Mohamed BM, Ibrahim ZAS, et al. Stem cell therapy as a novel therapeutic intervention for resistant cases of alopecia areata and androgenetic alopecia. J Dermatolog Treat. 2018;29(5):431–440. doi:10.1080/09546634.2016.1227419
    1. Gentile P, Scioli MG, Bielli A, Orlandi A, Cervelli V. Stem cells from human hair follicles: first mechanical isolation for immediate autologous clinical use in androgenetic alopecia and hair loss. Stem Cell Investig. 2017;4:58. doi:10.21037/sci.2017.06.04
    1. Álvarez X, Valenzuela M, Tuffet J. Clinical and histological evaluation of the Regenera®method for the treatment of androgenetic alopecia. Int Educ Appl Sci Res J. 2018;3(1):2456–5040.
    1. Ruiz RG, Rosell JMC, Ceccarelli G, et al. Progenitor-cell-enriched micrografts as a novel option for the management of androgenetic alopecia. J Cell Physiol. 2020;235(5):4587–4593. doi:10.1002/jcp.29335
    1. Kohn T, Zari S. Local anesthesia techniques in hair restoration surgery. J Cutan Med Surg. 2016;20(6):610–612. doi:10.1177/1203475416651052
    1. Kasprzak M, Sicińska J, Sinclair R. The trichoscopy derived Sinclair scale: enhancing visual assessment through quantitative trichoscopy. Australas J Dermatol. 2019;60(2):134–136. doi:10.1111/ajd.12964
    1. Purba TS, Haslam IS, Poblet E, et al. Human epithelial hair follicle stem cells and their progeny: current state of knowledge, the widening gap in translational research and future challenges. Bioessays. 2014;36(5):513–525. doi:10.1002/bies.201300166
    1. Turksen K. Tissue-Specific Stem Cell Niche. Springer; 2015.
    1. Zhang P, Kling RE, Ravuri SK, et al. A review of adipocyte lineage cells and dermal papilla cells in hair follicle regeneration. J Tissue Eng. 2014;5:2041731414556850. doi:10.1177/2041731414556850
    1. Greco V, Chen T, Rendl M, et al. A two-step mechanism for stem cell activation during hair regeneration. Cell Stem Cell. 2009;4(2):155–169. doi:10.1016/j.stem.2008.12.009
    1. Rabbani P, Takeo M, Chou W, et al. Coordinated activation of Wnt in epithelial and melanocyte stem cells initiates pigmented hair regeneration. Cell. 2011;145(6):941–955. doi:10.1016/j.cell.2011.05.004
    1. Tanimura S, Tadokoro Y, Inomata K, et al. Hair follicle stem cells provide a functional niche for melanocyte stem cells. Cell Stem Cell. 2011;8(2):177–187. doi:10.1016/j.stem.2010.11.029
    1. Lolli F, Pallotti F, Rossi A, et al. Androgenetic alopecia: a review. Endocrine. 2017;57(1):9–17. doi:10.1007/s12020-017-1280-y
    1. Goodarzi HR, Abbasi A, Saffari M, Fazelzadeh Haghighi M, Tabei MB, Noori Daloii MR. Differential expression analysis of balding and nonbalding dermal papilla microRNAs in male pattern baldness with a microRNA amplification profiling method. Br J Dermatol. 2012;166(5):1010–1016. doi:10.1111/j.1365-2133.2011.10675.x
    1. Inui S, Fukuzato Y, Nakajima T, Yoshikawa K, Itami S. Identification of androgen-inducible TGF- beta1 derived from dermal papilla cells as a key mediator in androgenetic alopecia. J Invest Dermatol Symp Proc. 2003;8(1):69–71. doi:10.1046/j.1523-1747.2003.12174.x
    1. Itami S, Inui S. Role of androgen in mesenchymal epithelial interactions in human hair follicle. J Invest Dermatol Symp Proc. 2005;10(3):209–211. doi:10.1111/j.1087-0024.2005.10107.x
    1. Leirós GJ, Ceruti JM, Castellanos ML, Kusinsky AG, Balañá ME. Androgens modify Wnt agonists/antagonists expression balance in dermal papilla cells preventing hair follicle stem cell differentiation in androgenetic alopecia. Mol Cell Endocrinol. 2017;439:26–34. doi:10.1016/j.mce.2016.10.018
    1. Shin H, Yoo HG, Inui S, et al. Induction of transforming growth factor-beta 1 by androgen is mediated by reactive oxygen species in hair follicle dermal papilla cells. BMB Rep. 2013;46(9):460–464. doi:10.5483/BMBRep.2013.46.9.228
    1. Yoo HG, Kim JS, Lee SR, et al. Perifollicular fibrosis: pathogenetic role in androgenetic alopecia. Biol Pharm Bull. 2006;29(6):1246–1250. doi:10.1248/bpb.29.1246
    1. Vasserot AP, Geyfman M, Poloso NJ. Androgenetic alopecia: combing the hair follicle signaling pathways for new therapeutic targets and more effective treatment options. Expert Opin Ther Targets. 2019;23(9):755–771. doi:10.1080/14728222.2019.1659779
    1. Zanzottera F, Lavezzari E, Trovato L, Icardi A, Graziano A. Adipose derived stem cells and growth factors applied on hair transplantation. Follow-up of clinical outcome. J Cosmetics Dermatol Sci Appl. 2014;2014. doi:10.4236/JCDSA.2014.44036

Source: PubMed

3
Suscribir