Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions

Review paper

Authors

  • Rinky Kapoor Department of Dermatology, Cosmetic Dermatology & Dermato-Surgery, The Esthetic Clinics, Mumbai, Maharashtra, India https://orcid.org/0009-0002-2443-878X
  • Depti Bellani Department of Medical Affairs, The Esthetic Creations International Pvt. Ltd. (ECIPL), Mumbai, Maharashtra, India https://orcid.org/0000-0003-1045-9758
  • Raji Patil Department of Medical Affairs, The Esthetic Creations International Pvt. Ltd. (ECIPL), Mumbai, Maharashtra, India. https://orcid.org/0009-0003-2725-7578
  • Debalina Bose Department of Research, The Esthetic Clinics Clinical Research Organization (TECCRO), Mumbai, Maharashtra, India https://orcid.org/0009-0005-0350-3839
  • Madhuri Pola Department of Research, The Esthetic Clinics Clinical Research Organization (TECCRO), Mumbai, Maharashtra, India https://orcid.org/0000-0003-3959-0223
  • Prashant Anilkumar Singh Department of Medical Affairs, The Esthetic Creations International Pvt. Ltd. (ECIPL), Mumbai, Maharashtra, India https://orcid.org/0009-0006-0427-6866
  • Mamata Mishra Department of Research, The Esthetic Clinics Clinical Research Organization (TECCRO), Mumbai, Maharashtra, India https://orcid.org/0000-0003-3797-7133
  • Debraj Shome Department of Facial Plastic Surgery & Facial Cosmetic Surgery, The Esthetic Clinics, Mumbai, Maharashtra, India https://orcid.org/0009-0007-8026-4629

DOI:

https://doi.org/10.5599/admet.3030

Keywords:

Androgenetic alopecia, alopecia areata, genome-wide association studies and next-generation sequencing, wingless-related integration sit/beta-catenin signalling pathway, Janus kinase-signal transducer and activator of transcription pathway, artificial intelligence

Abstract

Background and purpose: Non-scarring alopecia, principally androgenetic alopecia and alopecia areata is highly prevalent and psychologically burdensome; androgenetic alopecia is androgen-driven, whereas alopecia areata is autoimmune. This review synthesizes genetic architecture and pathway biology to outline a precision framework for targeted interventions. Experimental approach: We reviewed full-text studies from the past decade across PubMed, Web of Science and Google Scholar, applying explicit inclusion/ex­clusion criteria; emphasis was placed on Genome wide association studies and Next generation sequencing findings, immune and androgen-axis biology, environmental modifiers, and therapeutic evidence (conven­tional, targeted, and regenerative), alongside artificial Intelligence-enabled diagnostics. Key results: Andro­genetic alopecia risk converges on androgen-receptor signalling and related loci, with perifollicular inflam­mation and oxidative stress as modifiers; finasteride remains a cornerstone therapy. Alopecia areata reflects polygenic immune dysregulation (e.g. Human leukocyte antigen/cytokine axes) with Janus Kinase-pathway inhibition yielding robust regrowth; across phenotypes, wingless-related integration sit/β-catenin and stem-cell programs are central targets. Regenerative options (Protein Rich Plasma, stem-cell/exosome appro­aches) and artificial Intelligence-assisted stratification are emerging adjuncts. Conclusion: A pathway-guided, genotype and phenotype-informed strategy, targeting the androgen axis for androgenetic alopecia, immune circuits for alopecia areata, and adding regenerative or microenvironmental therapies where indicated-promises earlier diagnosis and more durable, individualized outcomes, especially as genome-wide association study/next-generation sequencing and artificial Intelligence tools are integrated into care.

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References

[1] L. Alhanshali, M.G. Buontempo, K.I. Lo Sicco, J. Shapiro. Alopecia Areata: Burden of Disease, Approach to Treatment, and Current Unmet Needs. Clinical, Cosmetic and Investigational Dermatology 16 (2023) 803-820. https://dx.doi.org/10.2147/ccid.S376096 DOI: https://doi.org/10.2147/CCID.S376096

[2] T.C. Anudeep, M. Jeyaraman, S. Muthu, R.L. Rajendran, P. Gangadaran, P.C. Mishra, S. Sharma, S.K. Jha, B.C. Ahn. Advancing Regenerative Cellular Therapies in Non-Scarring Alopecia. Pharmaceutics 14 (2022) 612. https://dx.doi.org/10.3390/pharmaceutics14030612 DOI: https://doi.org/10.3390/pharmaceutics14030612

[3] A. Martinez-Lopez, T. Montero-Vilchez, Á. Sierra-Sánchez, A. Molina-Leyva, S. Arias-Santiago. Advanced Medical Therapies in the Management of Non-Scarring Alopecia: Areata and Androgenic Alopecia. International Journal of Molecular Sciences 21 (2020) 8390. https://dx.doi.org/10.3390/ijms21218390 DOI: https://doi.org/10.3390/ijms21218390

[4] Y. Ibrahim, A. Hamed, A. Saeed, G. Khalik, E. Behiry. Evaluation of oxidative stress markers in Androgenetic Alopecia Patients. Benha Journal of Applied Sciences 8 (2023) 105-110. https://dx.doi.org/10.21608/bjas.2024.261687.1307 DOI: https://doi.org/10.21608/bjas.2024.261687.1307

[5] A. Kakunje, A. Prabhu, R. Pookoth, S. e S, R. Karkal, P. Kumar, N. Gupta. A perspective on predictive markers of alopecia. Archives of Medicine and Health Sciences 8 (2020) 263. https://dx.doi.org/10.4103/amhs.amhs_228_20 DOI: https://doi.org/10.4103/amhs.amhs_228_20

[6] M. van Dalen, K.S. Muller, J.M. Kasperkovitz-Oosterloo, J.M.E. Okkerse, S. Pasmans. Anxiety, depression, and quality of life in children and adults with alopecia areata: A systematic review and meta-analysis. Frontiers in Medicine (Lausanne) 9 (2022) 1054898. https://dx.doi.org/10.3389/fmed.2022.1054898 DOI: https://doi.org/10.3389/fmed.2022.1054898

[7] I. Šutić Udović, N. Hlača, L.P. Massari, I. Brajac, M. Kaštelan, M. Vičić. Deciphering the Complex Immunopathogenesis of Alopecia Areata. International Journal of Molecular Sciences 25 (2024) 5652. https://dx.doi.org/10.3390/ijms25115652 DOI: https://doi.org/10.3390/ijms25115652

[8] X. Luo, X. Ni, J. Zhi, X. Jiang, R. Bai. Small molecule agents against alopecia: Potential targets and related pathways. European Journal of Medicinal Chemistry 276 (2024) 116666. https://dx.doi.org/10.1016/j.ejmech.2024.116666 DOI: https://doi.org/10.1016/j.ejmech.2024.116666

[9] R.S. Ho. Ongoing Concerns Regarding Finasteride for the Treatment of Male-Pattern Androgenetic Alopecia. JAMA Dermatology 157 (2021) 25-26. https://dx.doi.org/10.1001/jamadermatol.2020.3384 DOI: https://doi.org/10.1001/jamadermatol.2020.3384

[10] X. Wang, Y. Liu, J. He, J. Wang, X. Chen, R. Yang. Regulation of signaling pathways in hair follicle stem cells. Burns & Trauma 10 (2022) tkac022. https://dx.doi.org/10.1093/burnst/tkac022 DOI: https://doi.org/10.1093/burnst/tkac022

[11] L.A. Mendoza, G.G. Ocampo, Y.A. Abarca-Pineda, M. Ahmad Khan, Y. Ahmadi, N. Brown, D. Deowan, Z. Nazir. Comprehensive Review on Hair Loss and Restorative Techniques: Advances in Diagnostic, Artistry, and Surgical Innovation. Cureus 17 (2025) e82991. https://dx.doi.org/10.7759/cureus.82991 DOI: https://doi.org/10.7759/cureus.82991

[12] C.Y. Ho, C.Y. Wu, J.Y. Chen, C.Y. Wu. Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review. Genes (Basel) 14 (2023) 1362. https://dx.doi.org/10.3390/genes14071362 DOI: https://doi.org/10.3390/genes14071362

[13] H. Englander, B. Paiewonsky, L. Castelo-Soccio. Alopecia Areata: A Review of the Genetic Variants and Immunodeficiency Disorders Associated with Alopecia Areata. Skin Appendage Disorders 9 (2023) 325-332. https://dx.doi.org/10.1159/000530432 DOI: https://doi.org/10.1159/000530432

[14] N. Gokce, N. Basgoz, S. Kenanoglu, H. Akalin, Y. Ozkul, M.C. Ergoren, T. Beccari, M. Bertelli, M. Dundar. An overview of the genetic aspects of hair loss and its connection with nutrition. Journal of Preventive Medicine and Hygiene 63 (2022) E228-e238. https://dx.doi.org/10.15167/2421-4248/jpmh2022.63.2S3.2765

[15] F.B. Basmanav, R.C. Betz. Translational impact of omics studies in alopecia areata: recent advances and future perspectives. Expert Review of Clinical Immunology 18 (2022) 845-857. https://dx.doi.org/10.1080/1744666x.2022.2096590 DOI: https://doi.org/10.1080/1744666X.2022.2096590

[16] K. Anastassakis. Androgenetic Alopecia From A to Z: Vol.1 Basic Science, Diagnosis, Etiology, and Related Disorders, Springer Nature, 2022. https://dx.doi.org/10.1007/978-3-030-76111-0 DOI: https://doi.org/10.1007/978-3-030-76111-0

[17] S. Amir, S.T.A. Shah, C. Mamoulakis, A.O. Docea, O.I. Kalantzi, A. Zachariou, D. Calina, F. Carvalho, N. Sofikitis, A. Makrigiannakis, A. Tsatsakis. Endocrine Disruptors Acting on Estrogen and Androgen Pathways Cause Reproductive Disorders through Multiple Mechanisms: A Review. International Journal of Environmental Research and Public Health 18 (2021) 1464. https://dx.doi.org/10.3390/ijerph18041464 DOI: https://doi.org/10.3390/ijerph18041464

[18] Z. Zhou, S. Song, Z. Gao, J. Wu, J. Ma, Y. Cui. The efficacy and safety of dutasteride compared with finasteride in treating men with androgenetic alopecia: a systematic review and meta-analysis. Clinical Interventions in Aging 14 (2019) 399-406. https://dx.doi.org/10.2147/cia.S192435 DOI: https://doi.org/10.2147/CIA.S192435

[19] U. Panich, G. Sittithumcharee, N. Rathviboon, S. Jirawatnotai. Ultraviolet Radiation-Induced Skin Aging: The Role of DNA Damage and Oxidative Stress in Epidermal Stem Cell Damage Mediated Skin Aging. Stem Cells International 2016 (2016) 7370642. https://dx.doi.org/10.1155/2016/7370642 DOI: https://doi.org/10.1155/2016/7370642

[20] A.A. Alotiby. Integrating Psychological Support and Topical Therapy for the Effective Management of Stress-Induced Alopecia Areata: A Case Report. Cureus 17 (2025) e77317. https://dx.doi.org/10.7759/cureus.77317 DOI: https://doi.org/10.7759/cureus.77317

[21] R. Cuevas-Diaz Duran, E. Martinez-Ledesma, M. Garcia-Garcia, D. Bajo Gauzin, A. Sarro-Ramírez, C. Gonzalez-Carrillo, D. Rodríguez-Sardin, A. Fuentes, A. Cardenas-Lopez. The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia. International Journal of Molecular Sciences 25 (2024) 2542. https://dx.doi.org/10.3390/ijms25052542 DOI: https://doi.org/10.3390/ijms25052542

[22] X. Zong, S. Yang, Z. Tang, X. Li, D. Long, D. Wang. 1,25-(OH)(2)D(3) promotes hair growth by inhibiting NLRP3/IL-1β and HIF-1α/IL-1β signaling pathways. Journal of Nutritional Biochemistry 132 (2024) 109695. https://dx.doi.org/10.1016/j.jnutbio.2024.109695 DOI: https://doi.org/10.1016/j.jnutbio.2024.109695

[23] R.M. Trüeb, H. Dutra Rezende, M.F.R. Gavazzoni Dias, D. Silva Polito, S. de Abreu Neves Salles. Bacterial diseases, in Hair in Infectious Disease: Recognition, Treatment, and Prevention, Springer, Cham, Switzerland, 2023, p. 35-127. https://doi.org/10.1007/978-3-031-30754-6 DOI: https://doi.org/10.1007/978-3-031-30754-6_3

[24] Y. Lin, X. Wu, Y. Yang, Y. Wu, L. Xiang, C. Zhang. The multifaceted role of autophagy in skin autoimmune disorders: a guardian or culprit? Frontiers in Immunology 15 (2024) 1343987. https://dx.doi.org/10.3389/fimmu.2024.1343987 DOI: https://doi.org/10.3389/fimmu.2024.1343987

[25] Y. Li, S. Yang, M. Liao, Z. Zheng, M. Li, X. Wei, M. Liu, L. Yang. Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study. Frontiers in Immunology 13 (2022) 1072573. https://dx.doi.org/10.3389/fimmu.2022.1072573 DOI: https://doi.org/10.3389/fimmu.2022.1072573

[26] P. Wu, K. Tian, S. Gao, Z. Jia, W. Xu, X. Wang, L. Wu. Interleukin-33 links asthma to alopecia areata: Mendelian randomization and mediation analysis. Skin Research and Technology 30 (2024) e13864. https://dx.doi.org/10.1111/srt.13864 DOI: https://doi.org/10.1111/srt.13864

[27] L. Pan, P. Moog, C. Li, L. Steinbacher, S. Knoedler, H. Kükrek, U. Dornseifer, H.G. Machens, J. Jiang. Exploring the Association Between Multidimensional Dietary Patterns and Non-Scarring Hair Loss Using Mendelian Randomization. Nutrients 17 (2025) 2569. https://dx.doi.org/10.3390/nu17152569 DOI: https://doi.org/10.3390/nu17152569

[28] A. Borde, A. Åstrand. Alopecia areata and the gut-the link opens up for novel therapeutic interventions. Expert Opinion on Therapeutic Targets 22 (2018) 503-511. https://dx.doi.org/10.1080/14728222.2018.1481504 DOI: https://doi.org/10.1080/14728222.2018.1481504

[29] J.Y. Lee, H.J. Lim, S.H. Kim, G.J. Lee, K.H. Nam, J. Park, J.K. Choi. Decreased CD19(+)CD24(hi)CD38(hi) Regulatory B Cells in Alopecia Areata. Journal of Investigative Dermatology 144 (2024) 2080-2083.e2087. https://dx.doi.org/10.1016/j.jid.2024.02.004 DOI: https://doi.org/10.1016/j.jid.2024.02.004

[30] N.A. Hibberts, A.E. Howell, V.A. Randall. Balding hair follicle dermal papilla cells contain higher levels of androgen receptors than those from non-balding scalp. Journal of Endocrinology 156 (1998) 59-65. https://dx.doi.org/10.1677/joe.0.1560059 DOI: https://doi.org/10.1677/joe.0.1560059

[31] R.C. Stone, A. Aviv, R. Paus. Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research. Journal of Investigative Dermatology 141 (2021) 1031-1040. https://dx.doi.org/10.1016/j.jid.2020.12.006 DOI: https://doi.org/10.1016/j.jid.2020.12.006

[32] M.P. Francès, L. Vila-Vecilla, V. Russo, H. Caetano Polonini, G.T. de Souza. Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment. Dermato-logy and Therapy (Heidelberg) 14 (2024) 971-981. https://dx.doi.org/10.1007/s13555-024-01142-y DOI: https://doi.org/10.1007/s13555-024-01142-y

[33] M. Murugan, I.P. Sadasivam, A. Manoharan, S. Jayakumar, Y. Vetriselvan, M.S. Samuel, R. Sambandam. Association between PITX2 polymorphism and androgenetic alopecia in the Indian population. Indian Journal of Dermatology, Venereology and Leprology 91 (2025) 158-162. https://dx.doi.org/10.25259/ijdvl_1147_2023 DOI: https://doi.org/10.25259/IJDVL_1147_2023

[34] R. Kucerova, M. Bienova, M. Kral, J. Bouchal, K.S. Trtkova, A. Burdova, V. Student, Z. Kolar. Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer. Journal of the European Academy of Dermatology and Venereology 29 (2015) 91-96. https://dx.doi.org/10.1111/jdv.12468 DOI: https://doi.org/10.1111/jdv.12468

[35] L. Vila-Vecilla, V. Russo, G. Souza. Genomic Markers and Personalized Medicine in Androgenetic Alopecia. Cosmetics 11 (2024) 148. https://dx.doi.org/10.3390/cosmetics11050148 DOI: https://doi.org/10.3390/cosmetics11050148

[36] M. Pu, J. Chen, Z. Tao, L. Miao, X. Qi, Y. Wang, J. Ren. Regulatory network of miRNA on its target: coordination between transcriptional and post-transcriptional regulation of gene expression. Cellular and Molecular Life Sciences 76 (2019) 441-451. https://dx.doi.org/10.1007/s00018-018-2940-7 DOI: https://doi.org/10.1007/s00018-018-2940-7

[37] S. Paul, I. Licona-Vázquez, F.I. Serrano-Cano, N. Frías-Reid, C. Pacheco-Dorantes, S. Pathak, S. Chakraborty, A. Srivastava. Current insight into the functions of microRNAs in common human hair loss disorders: a mini review. Human Cell 34 (2021) 1040-1050. https://dx.doi.org/10.1007/s13577-021-00540-0 DOI: https://doi.org/10.1007/s13577-021-00540-0

[38] D. Papukashvili, N. Rcheulishvili, C. Liu, F. Xie, D. Tyagi, Y. He, P.G. Wang. Perspectives on miRNAs Targeting DKK1 for Developing Hair Regeneration Therapy. Cells 10 (2021). https://dx.doi.org/10.3390/cells10112957 DOI: https://doi.org/10.3390/cells10112957

[39] H. Wei, T. Yi, Q. Li, Y. Guo, C. Shen, P. Jin. Application of lncRNA-miRNA-mRNA ceRNA network analysis in the treatment of androgenic alopecia. Journal of Clinical Laboratory Analysis 37 (2023) e24791. https://dx.doi.org/10.1002/jcla.24791 DOI: https://doi.org/10.1002/jcla.24791

[40] O.M. Atrooz, N. Reihani, M.R. Mozafari, A. Salawi, E. Taghavi. Enhancing hair regeneration: Recent progress in tailoring nanostructured lipid carriers through surface modification strategies. ADMET & DMPK 12 (2024) 431-462. https://dx.doi.org/10.5599/admet.2376 DOI: https://doi.org/10.5599/admet.2376

[41] Q. Chen, T. Yang, J. Cheng, Q. Zhao. Exploring the shared genetic mechanisms of atopic dermatitis and alopecia areata via bioinformatics approaches. Archives of Dermatological Research 317 (2025) 448. https://dx.doi.org/10.1007/s00403-025-04004-5 DOI: https://doi.org/10.1007/s00403-025-04004-5

[42] Y. Du, C. Lu, L. Bi, C. Wang, M. Zhao, Y. Ding, W. Fan. Causal effects of genetically determined metabolites on androgenetic alopecia: A two-sample Mendelian randomization analysis. Skin Research and Technology 30 (2024) e13732. https://dx.doi.org/10.1111/srt.13732 DOI: https://doi.org/10.1111/srt.13732

[43] J.A. Ellis, K.J. Scurrah, J.E. Cobb, S.G. Zaloumis, A.E. Duncan, S.B. Harrap. Baldness and the androgen receptor: the AR polyglycine repeat polymorphism does not confer susceptibility to androgenetic alopecia. Human Genetics 121 (2007) 451-457. https://dx.doi.org/10.1007/s00439-006-0317-8 DOI: https://doi.org/10.1007/s00439-006-0317-8

[44] D.A. Prodi, N. Pirastu, G. Maninchedda, A. Sassu, A. Picciau, M.A. Palmas, A. Mossa, I. Persico, M. Adamo, A. Angius, M. Pirastu. EDA2R is associated with androgenetic alopecia. Journal of Investigative Dermatology 128 (2008) 2268-2270. https://dx.doi.org/10.1038/jid.2008.60 DOI: https://doi.org/10.1038/jid.2008.60

[45] A. Elgobashy, N. El-Nefiawy, S. El-Sayed, S. Magdy, W. Abdelmoez. A Review on Androgenic Alopecia: Etiology, Pathogenesis, Pharmacological and Non-Pharmacological Treatment Approaches. Ain Shams Medical Journal 75 (2024) 587-602. https://dx.doi.org/10.21608/asmj.2024.299393.1282 DOI: https://doi.org/10.21608/asmj.2024.299393.1282

[46] Y. Shimomura, D. Agalliu, A. Vonica, V. Luria, M. Wajid, A. Baumer, S. Belli, L. Petukhova, A. Schinzel, A.H. Brivanlou, B.A. Barres, A.M. Christiano. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex. Nature 464 (2010) 1043-1047. https://dx.doi.org/10.1038/nature08875 DOI: https://doi.org/10.1038/nature08875

[47] G.J. Leirós, A.I. Attorresi, M.E. Balañá. Hair follicle stem cell differentiation is inhibited through cross-talk between Wnt/β-catenin and androgen signalling in dermal papilla cells from patients with androgenetic alopecia. British Journal of Dermatology 166 (2012) 1035-1042. https://dx.doi.org/10.1111/j.1365-2133.2012.10856.x DOI: https://doi.org/10.1111/j.1365-2133.2012.10856.x

[48] P. Mirmirani, M. Consolo, P. Oyetakin-White, E. Baron, P. Leahy, P. Karnik. Similar response patterns to topical minoxidil foam 5% in frontal and vertex scalp of men with androgenetic alopecia: a microarray analysis. British Journal of Dermatology 172 (2015) 1555-1561. https://dx.doi.org/10.1111/bjd.13399 DOI: https://doi.org/10.1111/bjd.13399

[49] T. Midorikawa, T. Chikazawa, T. Yoshino, K. Takada, S. Arase. Different gene expression profile observed in dermal papilla cells related to androgenic alopecia by DNA macroarray analysis. Journal of Dermatological Science 36 (2004) 25-32. https://dx.doi.org/10.1016/j.jdermsci.2004.05.001 DOI: https://doi.org/10.1016/j.jdermsci.2004.05.001

[50] L.A. Garza, Y. Liu, Z. Yang, B. Alagesan, J.A. Lawson, S.M. Norberg, D.E. Loy, T. Zhao, H.B. Blatt, D.C. Stanton, L. Carrasco, G. Ahluwalia, S.M. Fischer, G.A. FitzGerald, G. Cotsarelis. Prostaglandin D2 inhibits hair growth and is elevated in bald scalp of men with androgenetic alopecia. Science Translational Medicine 4 (2012) 126ra134. https://dx.doi.org/10.1126/scitranslmed.3003122 DOI: https://doi.org/10.1126/scitranslmed.3003122

[51] S. Heilmann, A.K. Kiefer, N. Fricker, D. Drichel, A.M. Hillmer, C. Herold, J.Y. Tung, N. Eriksson, S. Redler, R.C. Betz, R. Li, A. Kárason, D.R. Nyholt, K. Song, S.H. Vermeulen, S. Kanoni, G. Dedoussis, N.G. Martin, L.A. Kiemeney, V. Mooser, K. Stefansson, J.B. Richards, T. Becker, F.F. Brockschmidt, D.A. Hinds, M.M. Nöthen. Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. Journal of Investigative Dermatology 133 (2013) 1489-1496. https://dx.doi.org/10.1038/jid.2013.43 DOI: https://doi.org/10.1038/jid.2013.43

[52] V.H. Price. Treatment of hair loss. New England Journal of Medicine 341 (1999) 964-973. https://dx.doi.org/10.1056/nejm199909233411307 DOI: https://doi.org/10.1056/NEJM199909233411307

[53] D. Rathnayake, R. Sinclair. Male androgenetic alopecia. Expert Opinion on Pharmacotherapy 11 (2010) 1295-1304. https://dx.doi.org/10.1517/14656561003752730 DOI: https://doi.org/10.1517/14656561003752730

[54] M.H. Kwack, M.K. Kim, J.C. Kim, Y.K. Sung. Dickkopf 1 promotes regression of hair follicles. Journal of Investigative Dermatology 132 (2012) 1554-1560. https://dx.doi.org/10.1038/jid.2012.24 DOI: https://doi.org/10.1038/jid.2012.24

[55] K. Lingappan. NF-κB in Oxidative Stress. Current Opinion in Toxicology 7 (2018) 81-86. https://dx.doi.org/10.1016/j.cotox.2017.11.002 DOI: https://doi.org/10.1016/j.cotox.2017.11.002

[56] Z. Liu, X. Liu. Gut microbiome, metabolome and alopecia areata. Frontiers in Microbiology 14 (2023) 1281660. https://dx.doi.org/10.3389/fmicb.2023.1281660 DOI: https://doi.org/10.3389/fmicb.2023.1281660

[57] B. Liu, A. Li, Y. Liu, X. Ke, Q. Liu, X. Zuo, J. Xu, Y. Cui. Identification of Distinct Immune Signatures and Chemokine Networks in Scalp Inflammatory Diseases. Research Square (2023). https://doi.org/10.21203/rs.3.rs-3074741/v1 DOI: https://doi.org/10.21203/rs.3.rs-3074741/v1

[58] A.B. Coda, A.A. Sinha. Integration of genome-wide transcriptional and genetic profiles provides insights into disease development and clinical heterogeneity in alopecia areata. Genomics 98 (2011) 431-439. https://dx.doi.org/10.1016/j.ygeno.2011.08.009 DOI: https://doi.org/10.1016/j.ygeno.2011.08.009

[59] J.A. Ellis, M. Stebbing, S.B. Harrap. Polymorphism of the androgen receptor gene is associated with male pattern baldness. Journal of Investigative Dermatology 116 (2001) 452-455. https://dx.doi.org/10.1046/j.1523-1747.2001.01261.x DOI: https://doi.org/10.1046/j.1523-1747.2001.01261.x

[60] C.H. Ho, T. Sood, P.M. Zito. Androgenetic alopecia, in StatPearls [Internet], StatPearls Publishing, Treasure Island, Florida, 2024. https://www.ncbi.nlm.nih.gov/books/NBK430924/

[61] D. Bellani, R. Patil, A. Prabhughate, R. Shahare, M. Gold, R. Kapoor, D. Shome. Pathophysiological mechanisms of hair follicle regeneration and potential therapeutic strategies. Stem Cell Research & Therapy 16 (2025) 302. https://dx.doi.org/10.1186/s13287-025-04420-4 DOI: https://doi.org/10.1186/s13287-025-04420-4

[62] J. Kim, J. An, Y.K. Lee, G. Ha, H. Ban, H. Kong, H. Lee, Y. Song, C.K. Lee, S.B. Kim, K. Kim. Hair Growth Promoting Effects of Solubilized Sturgeon Oil and Its Correlation with the Gut Microbiome. Pharmaceuticals (Basel) 17 (2024) 1112. https://dx.doi.org/10.3390/ph17091112 DOI: https://doi.org/10.3390/ph17091112

[63] J. Li, X. Duan, F. Cheng, G. Li, Z.-L. Deng, L. Yang, J. Zhang, F. Liu, Y. Li, Z. Wu, T. Chen, B. Wang, X. Zhao, W. Shi, F. Xie, Y. Tang. Impaired Arginine Metabolism in Hair Follicles: A Potential Mechanism in Androgenetic Alopecia, Research square (2023). https://dx.doi.org/10.21203/rs.3.rs-3629594/v1 DOI: https://doi.org/10.21203/rs.3.rs-3629594/v1

[64] L.B. Zhou, Q. Cao, Q. Ding, W.L. Sun, Z.Y. Li, M. Zhao, X.W. Lin, G.P. Zhou, W.X. Fan. Transcription factor FOXC1 positively regulates SFRP1 expression in androgenetic alopecia. Experimental Cell Research 404 (2021) 112618. https://dx.doi.org/10.1016/j.yexcr.2021.112618 DOI: https://doi.org/10.1016/j.yexcr.2021.112618

[65] Y. Liu, S. Yang, Y. Zeng, Z. Tang, X. Zong, X. Li, C. Yang, L. Liu, X. Tong, L. Zhou, D. Wang. Dysregulated behaviour of hair follicle stem cells triggers alopecia and provides potential therapeutic targets. Experimental Dermatology 31 (2022) 986-992. https://dx.doi.org/10.1111/exd.14600 DOI: https://doi.org/10.1111/exd.14600

[66] W. Yu, Y. Mei, Z. Lu, L. Zhou, F. Jia, S. Chen, Z. Wang. The causal relationship between genetically determined telomere length and meningiomas risk. Frontiers in Neurology 14 (2023) 1178404. https://dx.doi.org/10.3389/fneur.2023.1178404 DOI: https://doi.org/10.3389/fneur.2023.1178404

[67] J. Xiong, B. Wu, Q. Hou, X. Huang, L. Jia, Y. Li, H. Jiang. Comprehensive Analysis of LncRNA AC010789.1 Delays Androgenic Alopecia Progression by Targeting MicroRNA-21 and the Wnt/β-Catenin Signaling Pathway in Hair Follicle Stem Cells. Frontiers in Genetics 13 (2022) 782750. https://dx.doi.org/10.3389/fgene.2022.782750 DOI: https://doi.org/10.3389/fgene.2022.782750

[68] P. Mohammadi, M.A. Nilforoushzadeh, K.K. Youssef, A. Sharifi-Zarchi, S. Moradi, P. Khosravani, R. Aghdami, P. Taheri, G. Hosseini Salekdeh, H. Baharvand, N. Aghdami. Defining microRNA signatures of hair follicular stem and progenitor cells in healthy and androgenic alopecia patients. Journal of Dermatological Science 101 (2021) 49-57. https://dx.doi.org/10.1016/j.jdermsci.2020.11.002 DOI: https://doi.org/10.1016/j.jdermsci.2020.11.002

[69] W. Deng, T. Hu, L. Han, B. Liu, X. Tang, H. Chen, X. Chen, M. Wan. miRNA microarray profiling in patients with androgenic alopecia and the effects of miR-133b on hair growth. Experimental and Molecular Pathology 118 (2021) 104589. https://dx.doi.org/10.1016/j.yexmp.2020.104589 DOI: https://doi.org/10.1016/j.yexmp.2020.104589

[70] S.W. Choi, T.S. Mak, P.F. O'Reilly. Tutorial: a guide to performing polygenic risk score analyses. Nature Protocols 15 (2020) 2759-2772. https://dx.doi.org/10.1038/s41596-020-0353-1 DOI: https://doi.org/10.1038/s41596-020-0353-1

[71] H. Moravvej, M.R. Pourani, M. Baghani, F. Abdollahimajd. Androgenetic alopecia and COVID-19: A review of the hypothetical role of androgens. Dermatologic Therapy 34 (2021) e15004. https://dx.doi.org/10.1111/dth.15004 DOI: https://doi.org/10.1111/dth.15004

[72] J. Xiong, G. Chen, Z. Liu, X. Wu, S. Xu, J. Xiong, S. Ji, M. Wu. Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms. Precision Clinical Medicine 6 (2023) pbad009. https://dx.doi.org/10.1093/pcmedi/pbad009 DOI: https://doi.org/10.1093/pcmedi/pbad009

[73] Q. Zhou, L. Lan, W. Wang, X. Xu. Identifying effective immune biomarkers in alopecia areata diagnosis based on machine learning methods. BMC Medical Informatics and Decision Making 25 (2025) 23. https://dx.doi.org/10.1186/s12911-025-02853-8 DOI: https://doi.org/10.1186/s12911-025-02853-8

[74] D. Ahn, H. Kim, B. Lee, D.H. Hahm. Psychological Stress-Induced Pathogenesis of Alopecia Areata: Autoimmune and Apoptotic Pathways. International Journal of Molecular Sciences 24 (2023) 11711. https://dx.doi.org/10.3390/ijms241411711 DOI: https://doi.org/10.3390/ijms241411711

[75] F. Lolli, F. Pallotti, A. Rossi, M.C. Fortuna, G. Caro, A. Lenzi, A. Sansone, F. Lombardo. Androgenetic alopecia: a review. Endocrine 57 (2017) 9-17. https://dx.doi.org/10.1007/s12020-017-1280-y DOI: https://doi.org/10.1007/s12020-017-1280-y

[76] P. Suchonwanit, S. Thammarucha, K. Leerunyakul. Minoxidil and its use in hair disorders: a review. Drug Design, Development and Therapy 13 (2019) 2777-2786. https://dx.doi.org/10.2147/dddt.S214907 DOI: https://doi.org/10.2147/DDDT.S214907

[77] A.K. Gupta, M. Venkataraman, M. Talukder, M.A. Bamimore. Finasteride for hair loss: a review. Journal of Dermatological Treatment 33 (2022) 1938-1946. https://dx.doi.org/10.1080/09546634.2021.1959506 DOI: https://doi.org/10.1080/09546634.2021.1959506

[78] V.W.Y. Lai, R. Sinclair. Utility of azathioprine, methotrexate and cyclosporine as steroid-sparing agents in chronic alopecia areata: a retrospective study of continuation rates in 138 patients. Journal of the European Academy of Dermatology and Venereology 34 (2020) 2606-2612. https://dx.doi.org/10.1111/jdv.16858 DOI: https://doi.org/10.1111/jdv.16858

[79] M. Lensing, A. Jabbari. An overview of JAK/STAT pathways and JAK inhibition in alopecia areata. Frontiers in Immunology 13 (2022) 955035. https://dx.doi.org/10.3389/fimmu.2022.955035 DOI: https://doi.org/10.3389/fimmu.2022.955035

[80] A. Samadi, S. Ahmad Nasrollahi, A. Hashemi, M. Nassiri Kashani, A. Firooz. Janus kinase (JAK) inhibitors for the treatment of skin and hair disorders: a review of literature. Journal of Dermatological Treatment 28 (2017) 476-483. https://dx.doi.org/10.1080/09546634.2016.1277179 DOI: https://doi.org/10.1080/09546634.2016.1277179

[81] K.D. Kaufman, E.A. Olsen, D. Whiting, R. Savin, R. DeVillez, W. Bergfeld, V.H. Price, D. Van Neste, J.L. Roberts, M. Hordinsky, J. Shapiro, B. Binkowitz, G.J. Gormley. Finasteride in the treatment of men with androgenetic alopecia. Finasteride Male Pattern Hair Loss Study Group. Journal of the American Academy of Dermatology 39 (1998) 578-589. https://dx.doi.org/10.1016/s0190-9622(98)70007-6 DOI: https://doi.org/10.1016/S0190-9622(98)70007-6

[82] R.M. Trüeb. Oxidative stress in ageing of hair. International Journal of Trichology 1 (2009) 6-14. https://dx.doi.org/10.4103/0974-7753.51923 DOI: https://doi.org/10.4103/0974-7753.51923

[83] N.J. Hawkshaw, J.A. Hardman, I.S. Haslam, A. Shahmalak, A. Gilhar, X. Lim, R. Paus. Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles. PLoS Biology 16 (2018) e2003705. https://dx.doi.org/10.1371/journal.pbio.2003705 DOI: https://doi.org/10.1371/journal.pbio.2003705

[84] D.H. Bak, M.J. Choi, S.R. Kim, B.C. Lee, J.M. Kim, E.S. Jeon, W. Oh, E.S. Lim, B.C. Park, M.J. Kim, J. Na, B.J. Kim. Human umbilical cord blood mesenchymal stem cells engineered to overexpress growth factors accelerate outcomes in hair growth. Korean Journal of Physiology & Pharmacology 22 (2018) 555-566. https://dx.doi.org/10.4196/kjpp.2018.22.5.555 DOI: https://doi.org/10.4196/kjpp.2018.22.5.555

[85] A.R. Yuan, Q. Bian, J.Q. Gao. Current advances in stem cell-based therapies for hair regeneration. European Journal of Pharmacology 881 (2020) 173197. https://dx.doi.org/10.1016/j.ejphar.2020.173197 DOI: https://doi.org/10.1016/j.ejphar.2020.173197

[86] P. Gentile, M.G. Scioli, A. Bielli, B. De Angelis, C. De Sio, D. De Fazio, G. Ceccarelli, A. Trivisonno, A. Orlandi, V. Cervelli, S. Garcovich. Platelet-Rich Plasma and Micrografts Enriched with Autologous Human Follicle Mesenchymal Stem Cells Improve Hair Re-Growth in Androgenetic Alopecia. Biomolecular Pathway Analysis and Clinical Evaluation. Biomedicines 7 (2019) 27. https://dx.doi.org/10.3390/biomedicines7020027 DOI: https://doi.org/10.3390/biomedicines7020027

[87] D.W. Shin. The physiological and pharmacological roles of prostaglandins in hair growth. Korean Journal of Physiology & Pharmacology 26 (2022) 405-413. https://dx.doi.org/10.4196/kjpp.2022.26.6.405 DOI: https://doi.org/10.4196/kjpp.2022.26.6.405

[88] J.Y. Choi, M.Y. Boo, Y.C. Boo. Can Plant Extracts Help Prevent Hair Loss or Promote Hair Growth? A Review Comparing Their Therapeutic Efficacies, Phytochemical Components, and Modulatory Targets. Molecules 29 (2024) 2288. https://dx.doi.org/10.3390/molecules29102288 DOI: https://doi.org/10.3390/molecules29102288

[89] B. Rafidi, K. Kondapi, M. Beestrum, S. Basra, P. Lio. Psychological Therapies and Mind-Body Techniques in the Management of Dermatologic Diseases: A Systematic Review. American Journal of Clinical Dermatology 23 (2022) 755-773. https://dx.doi.org/10.1007/s40257-022-00714-y DOI: https://doi.org/10.1007/s40257-022-00714-y

[90] Y. Zou, F. Tang, P. Li, W. Qiu, M. Lei. Wnt10b Regulation of Hair Follicle Development, Regeneration, and Skin Diseases. Stem Cell Reviews and Reports 21 (2025) 1728-1737. https://dx.doi.org/10.1007/s12015-025-10898-5 DOI: https://doi.org/10.1007/s12015-025-10898-5

[91] R. Kapoor, D. Shome, S. Vadera, V. Kumar, M.S. Ram. QR678 & QR678 Neo Hair Growth Formulations: A Cellular Toxicity & Animal Efficacy Study. Plastic and Reconstructive Surgery Global Open 8 (2020) e2843. https://dx.doi.org/10.1097/gox.0000000000002843 DOI: https://doi.org/10.1097/GOX.0000000000002843

[92] BioSpace. Scientists Decode Hair Loss at the Molecular Level, Paving the Way for Regrowth Without Transplants. BioSpace (2025). https://www.biospace.com/press-releases/scientists-decode-hair-loss-at-the-molecular-level-paving-the-way-for-regrowth-without-transplants (date accessed on 30th July 2025)

[93] D. Shome, R. Kapoor, K. Doshi, G. Patel, S. Vadera, V. Kumar. Effectiveness of QR678 and QR678 Neo(®) with intralesional corticosteroid vs. intralesional corticosteroid alone in the treatment of alopecia areata - A randomized, comparative, prospective study. Journal of Cosmetic Dermatology 21 (2022) 358-367. https://dx.doi.org/10.1111/jocd.14630 DOI: https://doi.org/10.1111/jocd.14630

[94] D. Shome, R. Kapoor, M. Surana, S. Vadera, R. Shah. Efficacy of QR678 Neo(®) hair growth factor formulation for the treatment of hair loss in Covid-19-induced persistent Telogen Effluvium - A prospective, clinical, single-blind study. Journal of Cosmetic Dermatology 21 (2022) 16-23. https://dx.doi.org/10.1111/jocd.14626 DOI: https://doi.org/10.1111/jocd.14626

[95] A. Clinic, A. Asper, A. Mittal, D. Shome, D. Parbhoo, J. Thanzama, K. Doshi, N. Sachde, R. Gaunkar, R. Kapoor, R. Thakkar, S. Sion, S. Shetty, V. Kumar, V. Parveen, V. Singhal. Evaluation of the safety and effectiveness of intradermal administration of QR678 Neo(®) hair growth factor formulation: A phase-IV, open-label, single-arm multi-ethnicity clinical trial. Journal of Cosmetic Dermatology 21 (2022) 580-589. https://dx.doi.org/10.1111/jocd.14715 DOI: https://doi.org/10.1111/jocd.14715

[96] R. Kapoor, D. Shome, K. Doshi, G. Patel, S. Vadera. Evaluation of efficacy of QR 678 and QR678 neo hair growth factor formulation for the treatment of female pattern alopecia in patients with PCOS - A prospective study. Journal of Cosmetic Dermatology 19 (2020) 2637-2646. https://dx.doi.org/10.1111/jocd.13673 DOI: https://doi.org/10.1111/jocd.13673

[97] R. Kapoor, D. Shome, S. Vadera, M.S. Ram. QR 678 & QR678 Neo Vs PRP - A randomised, comparative, prospective study. Journal of Cosmetic Dermatology 19 (2020) 2877-2885. https://dx.doi.org/10.1111/jocd.13398 DOI: https://doi.org/10.1111/jocd.13398

[98] V. Kumar, D. Shome, S. Atre, A. Nagarsekar, R. Gaunkar, R. Kapoor, K. Doshi. The iceberg phenomenon of alopecia associated public health ramifications on the quality of life among adults in India. Dermatological Reviews (2022). https://dx.doi.org/10.1002/der2.109 DOI: https://doi.org/10.1002/der2.109

[99] V. Kumar, M. Gold, A. Jain, P. Mhatre, U. Zaman, R. Kapoor, D. Shome. Effectiveness of minimally invasive injectable modalities in the management of androgenetic alopecia among adults - A systematic review. Journal of Cosmetic Dermatology 23 (2024) 3144-3157. https://dx.doi.org/10.1111/jocd.16493 DOI: https://doi.org/10.1111/jocd.16493

[100] R. Kapoor, D. Shome, K. Doshi, G. Patel, H. Tandel, V. Kumar. A newer approach in the treatment of seborrheic dermatitis with QR678® and QR678 Neo® - A prospective pilot study. Journal of Cosmetic Dermatology 22 (2023) 3078-3087. https://dx.doi.org/10.1111/jocd.15957 DOI: https://doi.org/10.1111/jocd.15957

[101] R. Kapoor, D. Shome, K. Doshi, S. Vadera, G. Patel, V. Kumar. Evaluation of efficacy of QR678® and QR678® Neo hair growth factor formulation in the treatment of persistent chemotherapy‐induced alopecia caused due to cytotoxic chemotherapy—A prospective pilot study. Journal of Cosmetic Dermatology 19 (2020) 3270-3279. https://dx.doi: 10.1111/jocd.13759 DOI: https://doi.org/10.1111/jocd.13759

[102] D. Shome, R. Kapoor, S. Vadera, K. Doshi, G. Patel, T. Mohammad Khan. Evaluation of efficacy of intradermal injection therapy vs derma roller application for administration of QR678 Neo(®) hair regrowth formulation for the treatment of Androgenetic Alopecia - A prospective study. Journal of Cosmetic Dermatology 20 (2021) 3299-3307. https://dx.doi.org/10.1111/jocd.14139 DOI: https://doi.org/10.1111/jocd.14139

[103] D. Shome, H. Tandel, V. Kumar, R. Kapoor. Evaluation of efficacy of derma roller sizes vs topical application for administration of QR678 Neo® hair regrowth formulation in the treatment of androgenetic alopecia. Journal of Cosmetic Dermatology 21 (2022) 6528-6530. https://dx.doi.org/10.1111/jocd.15336 DOI: https://doi.org/10.1111/jocd.15336

[104] R. Kapoor, D. Shome. Intradermal injections of a hair growth factor formulation for enhancement of human hair regrowth - safety and efficacy evaluation in a first-in-man pilot clinical study. Journal of Cosmetic and Laser Therapy 20 (2018) 369-379. https://dx.doi.org/10.1080/14764172.2018.1439965 DOI: https://doi.org/10.1080/14764172.2018.1439965

[105] D. Shome, R. Kapoor, K. Doshi, G. Patel, S. Vadera, V. Kumar. Comparison of QR 678(®) & QR678(®) Neo as monotherapy and as combination therapy with 5% Minoxidil solution and oral Finasteride in the treatment of male androgenetic alopecia - Which is better? Journal of Cosmetic Dermatology 20 (2021) 1763-1765. https://dx.doi.org/10.1111/jocd.14154 DOI: https://doi.org/10.1111/jocd.14154

[106] M. Gold, U. Zaman, V. Chouksey, M. Gosavi. Evaluation of the efficacy of a biomimetic peptide solution for rejuvenation of donor scalp and as storage media for hair follicle grafts during FUE hair transplantation. Journal of Cosmetic and Laser Therapy 27 (2025) 64-70. https://dx.doi.org/10.1080/14764172.2025.2468499 DOI: https://doi.org/10.1080/14764172.2025.2468499

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16-12-2025

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Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions: Review paper. (2025). ADMET and DMPK, 14, 3030. https://doi.org/10.5599/admet.3030

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