# Research Progress on Platelet‐Rich Plasma (PRP) in the Treatment of Androgenetic Alopecia

**Authors:** Zetian Zhong, Li Luo, Lixiang Zhao, Xupeng Yue, Yanxin Lu

PMC · DOI: 10.1111/jocd.70809 · 2026-03-24

## TL;DR

This review explores how platelet-rich plasma (PRP) can help treat hair loss, showing it's safe and effective when combined with other therapies.

## Contribution

The paper provides a comprehensive review of PRP's mechanisms, clinical outcomes, and protocol recommendations for treating androgenetic alopecia.

## Key findings

- PRP promotes hair growth by activating key signaling pathways like Wnt/β-catenin and MAPK.
- Combining PRP with minoxidil or microneedling improves hair density and patient satisfaction.
- Adverse effects are mild, but protocol inconsistencies limit outcome reliability.

## Abstract

Androgenetic alopecia (AGA) is the most common cause of progressive hair loss, significantly affecting quality of life. Current therapies, such as minoxidil, finasteride, and hair transplantation, show variable efficacy and may be associated with adverse effects. Platelet‐rich plasma (PRP), an autologous preparation enriched with platelets and growth factors, has recently gained attention as a regenerative option for hair restoration.

This review summarizes advances in PRP therapy for AGA, focusing on preparation techniques, mechanisms of action, clinical efficacy, and safety, and provides recommendations for protocol optimization and future research.

A systematic search of PubMed, Web of Science, Embase, Cochrane Library, and CNKI was conducted for studies published between 2000 and 2025. Eligible articles included randomized controlled trials, cohort studies, case–control studies, and meta‐analyses evaluating PRP preparation methods or therapeutic outcomes. Study quality was appraised using the Cochrane Risk of Bias, ROBINS‐I, and GRADE frameworks.

PRP promotes follicular regeneration through angiogenesis and activation of Wnt/β‐catenin, MAPK, Akt/ERK, and Notch signaling pathways. Clinical trials demonstrate improved hair density, thickness, and patient satisfaction, particularly when PRP is combined with minoxidil, microneedling, or laser therapy. Reported adverse events are mild and transient, such as localized pain or erythema. Nevertheless, heterogeneity in centrifugation, activation, and delivery protocols contributes to inconsistent outcomes across studies.

PRP represents a promising, safe, and minimally invasive therapy for AGA. Establishing standardized preparation protocols and conducting large‐scale randomized studies are essential to confirm long‐term efficacy and integrate PRP into routine, personalized AGA management.

## Linked entities

- **Chemicals:** minoxidil (PubChem CID 4201), finasteride (PubChem CID 57363)
- **Diseases:** androgenetic alopecia (MONDO:0005339)

## Full-text entities

- **Genes:** CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, FGF7 (fibroblast growth factor 7) [NCBI Gene 2252] {aka HBGF-7, KGF}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, Lgr5 (leucine rich repeat containing G protein coupled receptor 5) [NCBI Gene 14160] {aka FEX, Gpr49}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345] {aka D630048A14Rik, Ki-67, Ki67}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** erectile dysfunction (MESH:D007172), hypertrichosis (MESH:D006983), inflammatory (MESH:D007249), diminished libido (MESH:D015354), suicidal ideation (MESH:D001072), swelling (MESH:D004487), follicular degeneration (MESH:D009410), erythema (MESH:D004890), sexual dysfunction (MESH:D012735), ejaculate volume (MESH:D061686), AGA (MESH:D000505), pain (MESH:D010146), seborrheic alopecia (MESH:D012628), hematologic disorders (MESH:D006402), allergic contact dermatitis (MESH:D017449), infection (MESH:D007239), pruritus (MESH:D011537), depression (MESH:D003866), contact dermatitis (MESH:D003877), hair (MESH:D006201)
- **Chemicals:** CO2 (MESH:D002245), calcium gluconate (MESH:D002125), finasteride (MESH:D018120), calcium chloride (MESH:D002122), Minoxidil (MESH:D008914), LDOM (-), calcium (MESH:D002118), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13013732/full.md

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Source: https://tomesphere.com/paper/PMC13013732