Retinoids in the treatment of photoageing: A histological study of topical retinoid efficacy in black skin

Author:

Halai P.1,Kiss O.1,Wang R.2,Chien A. L.2,Kang S.2,O'Connor C.3,Bell M.3,Griffiths C. E. M.14ORCID,Watson R. E. B.15,Langton A. K.1ORCID

Affiliation:

1. Centre for Dermatology Research The University of Manchester & Salford Royal NHS Foundation Trust, Manchester Academic Health Science Centre Manchester UK

2. Department of Dermatology Johns Hopkins University School of Medicine Baltimore Maryland USA

3. No7 Beauty Company, Walgreens Boots Alliance Nottingham UK

4. Department of Dermatology, King's College Hospital King's College London London UK

5. A*STAR Skin Research Laboratory (A*SRL) Agency for Science, Technology and Research (A*STAR) Singapore Singapore

Abstract

AbstractBackgroundPhotoageing describes complex cutaneous changes that occur due to chronic exposure to solar ultraviolet radiation (UVR). The ‘gold standard’ for the treatment of photoaged white skin is all‐trans retinoic acid (ATRA); however, cosmetic retinol (ROL) has also proven efficacious. Recent work has identified that black skin is susceptible to photoageing, characterized by disintegration of fibrillin‐rich microfibrils (FRMs) at the dermal–epidermal junction (DEJ). However, the impact of topical retinoids for repair of black skin has not been well investigated.ObjectivesTo determine the potential of retinoids to repair photoaged black skin.MethodsAn exploratory intervention study was performed using an in vivo, short‐term patch test protocol. Healthy but photoaged black volunteers (>45 years) were recruited to the study, and participant extensor forearms were occluded with either 0.025% ATRA (n = 6; 4‐day application due to irritancy) or ROL (12‐day treatment protocol for a cosmetic) at concentrations of 0.3% (n = 6) or 1% (n = 6). Punch biopsies from occluded but untreated control sites and retinoid‐treated sites were processed for histological analyses of epidermal characteristics, melanin distribution and dermal remodelling.ResultsTreatment with ATRA and ROL induced significant acanthosis (all p < 0.001) accompanied by a significant increase in keratinocyte proliferation (Ki67; all p < 0.01), dispersal of epidermal melanin and restoration of the FRMs at the DEJ (all p < 0.01), compared to untreated control.ConclusionsThis study confirms that topical ATRA has utility for the repair of photoaged black skin and that ROL induces comparable effects on epidermal and dermal remodelling, albeit over a longer timeframe. The effects of topical retinoids on black photoaged skin are similar to those reported for white photoaged skin and suggest conserved biology in relation to repair of UVR‐induced damage. Further investigation of topical retinoid efficacy in daily use is warranted for black skin.

Funder

Manchester Biomedical Research Centre

Biotechnology and Biological Sciences Research Council

Publisher

Wiley

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