Evidence map›Paper›PMID 42234321›Full record

ReviewDermatology and therapy2026

Decoding Hyperpigmentation from Biological Mechanisms to Actives with Clinically Proven Topical Efficacy: A Narrative Review.

Christine Duval, Jie Qiu, Emilie Warrick, Peggy Sextius, Isabelle Castiel-Higounenc, Leihong Xiang, Francoise Bernerd, Thierry Passeron

Abstract readReview
In one paragraph

Review in Dermatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Microorganisms · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Christine Duval *L'Oréal Research and Innovation, 1, Avenue Eugène Schueller, 93601, Aulnay-Sous-Bois, France.ORCID http://orcid.org/0000-0003-0982-2177
Jie Qiu *L'Oréal Research and Innovation, Shanghai, People's Republic of China.ORCID http://orcid.org/0009-0006-9149-3550
Emilie WarrickL'Oréal Research and Innovation, 1, Avenue Eugène Schueller, 93601, Aulnay-Sous-Bois, France.ORCID http://orcid.org/0000-0001-7589-7965
Peggy SextiusL'Oréal Research and Innovation, 1, Avenue Eugène Schueller, 93601, Aulnay-Sous-Bois, France.ORCID http://orcid.org/0000-0002-8710-6582
Isabelle Castiel-HigounencL'Oréal Research and Innovation, Clichy, France.ORCID http://orcid.org/0009-0008-8540-0834
Leihong XiangDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, People's Republic of China.ORCID http://orcid.org/0000-0003-2080-0550
Francoise BernerdL'Oréal Research and Innovation, 1, Avenue Eugène Schueller, 93601, Aulnay-Sous-Bois, France. fbernerd1@gmail.com.ORCID http://orcid.org/0000-0001-5426-7948
Thierry PasseronDepartment of Dermatology, Université Côte d'Azur, CHU Nice, Nice, France. passeron@unice.fr.ORCID http://orcid.org/0000-0002-0797-6570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperpigmentation disorders affect a large proportion of the population, significantly impacting their quality of life and carrying considerable social stigma. This growing global concern results in a strong demand for effective treatments. A rich body of literature proposes numerous active ingredients to solve hyperpigmentation concerns. At the same time, the complex regulation of skin pigmentation is much better understood with increased knowledge on the physiopathology of pigmentary disorders, beyond the sole melanogenesis, including the whole tissue environment of melanocytes. The abundance of mechanistic in vitro and in vivo scientific data makes it challenging for non-expert clinicians to identify the optimal care for patients. The aim of this review is to propose state-of-the-art of topical solutions with actives that have demonstrated conclusive clinical efficacy. It analyzes the different mechanisms involved, including the melanogenesis pathway and others addressing the melanocyte microenvironment. This review first examines the prevention of pigmentary disorders and the importance of a broad-spectrum photoprotection including the whole UV spectrum but also visible light in managing hyperpigmentation. The use of antioxidants to combat oxidative stress and complement photoprotection is also discussed. The following section reviews actives targeting the modulation of melanogenesis. It examines tyrosinase inhibitors, which are still widely used to manage hyperpigmentation problems, as well as new compounds targeting downstream pathways. Other clinically effective interventions include the normalization of epidermal homeostasis and the active restoration of the dermal fibroblastic microenvironment, together with anti-inflammatory agents and those aimed at reducing vascularization impact. Finally, this review highlights the value of combined approaches which have been shown to improve clinical efficacy. This suggests that future research should focus on well-tolerated, multifaceted therapies to effectively treat melanin hyperpigmentary disorders.

Indexed as

HyperpigmentationMelanogenesisPigmentary disorderTopical actives

Identifiers

PMID42234321
PMCPMC13280301

What Socratic holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.