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Hair regrowth treatment efficacy and resistance in androgenetic alopecia: A systematic review and continuous Bayesian network meta-analysis.
Feldman, Peter R; Gentile, Pietro; Piwko, Charles; Motswaledi, Hendrik M; Gorun, Samantha; Pesachov, Jacob; Markel, Michael; Silver, Maxwell I; Brenkel, Megan; Feldman, Oriel J; Kamen, Corey L; Uleryk, Elizabeth; Guevara-Aguirre, Jaime; Fiebig, Klaus M.
Afiliação
  • Feldman PR; Arbor Life Labs, Toronto, ON, Canada.
  • Gentile P; Norwich Medical School, University of East Anglia, Norwich, United Kingdom.
  • Piwko C; Surgical Science Department, University of Rome Tor Vergata, Rome, Italy.
  • Motswaledi HM; CHP Pharma Inc., Thornhill, ON, Canada.
  • Gorun S; Department of Dermatology, Sefako Makgatho Health Sciences University, Pretoria, South Africa.
  • Pesachov J; Faculty of Epidemiology and Biostatistics, Western University, London, ON, Canada.
  • Markel M; School or Mathematics and Statistics, University of Glasgow, Glasgow, United Kingdom.
  • Silver MI; Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
  • Brenkel M; Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
  • Feldman OJ; Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.
  • Kamen CL; Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.
  • Uleryk E; Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
  • Guevara-Aguirre J; Arbor Life Labs, Toronto, ON, Canada.
  • Fiebig KM; Faculty of Science, Wilfrid Laurier University, Waterloo, ON, Canada.
Front Med (Lausanne) ; 9: 998623, 2022.
Article em En | MEDLINE | ID: mdl-36755885
ABSTRACT

Background:

Androgenetic alopecia (AGA) affects almost half the population, and several treatments intending to regenerate a normal scalp hair phenotype are used. This is the first study comparing treatment efficacy response and resistance using standardized continuous outcomes.

Objective:

To systematically compare the relative efficacy of treatments used for terminal hair (TH) regrowth in women and men with AGA.

Methods:

A systematic literature review was conducted (from inception to August 11, 2021) to identify randomized, Placebo-controlled trials with ≥ 20 patients and reporting changes in TH density after 24 weeks. Efficacy was analyzed by sex at 12 and 24 weeks using Bayesian network meta-analysis (B-NMA) and compared to frequentist and continuous outcomes profiles.

Results:

The search identified 2,314 unique articles. Ninety-eight were included for full-text review, and 17 articles met the inclusion criteria for data extraction and analyses. Eligible treatments included ALRV5XR, Dutasteride 0.5 mg/day, Finasteride 1 mg/day, low-level laser comb treatment (LLLT), Minoxidil 2% and 5%, Nutrafol, and Viviscal. At 24 weeks, the B-NMA regrowth efficacy in TH/cm2 and significance (**) in women were ALRV5XR 30.09**, LLLT 16.62**, Minoxidil 2% 12.13**, Minoxidil 5% 10.82**, and Nutrafol 7.32**, and in men; ALRV5XR 21.03**, LLLT 18.75**, Dutasteride 18.37**, Viviscal 13.23, Minoxidil 5% 13.13**, Finasteride 12.38, and Minoxidil 2% 10.54. Two distinct TH regrowth response profiles were found; Continuous ALRV5XR regrowth rates were linear in men and accelerated in women; Resistant after 12 weeks, LLLT, Nutrafol, and Viviscal regrowth rates attenuated while Dutasteride and Finasteride plateaued; Minoxidil 2% and 5% lost some regrowth. There were no statistical differences for the same treatment between women and men. B-NMA provided more accurate, statistically relevant, and conservative results than the frequentist-NMA.

Conclusion:

Some TH regrowth can be expected from most AGA treatments with less variability in women than men. Responses to drug treatments were rapid, showing strong early efficacy followed by the greatest resistance effects from flatlining to loss of regrowth after 12-16 weeks. Finasteride, Minoxidil 2% and Viviscal in men were not statistically different from Placebo. LLLT appeared more efficacious than pharmaceuticals. The natural product formulation ALRV5XR showed better efficacy in all tested parameters without signs of treatment resistance (see Graphical abstract). Systematic review registration www.crd.york.ac.uk/PROSPERO/display_record.asp?ID=CRD42021268040, identifier CRD42021268040.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article