Evidence map›Paper›PMID 40485245›Full record

ArticleJournal of the European Academy of Dermatology and Venereology : JEADV2026

Clinical heterogeneity in vitiligo: Identification of clinical markers based patient clusters.

Laura Galissi, Tristan Benoît, Ribal Merhi, Claire Drullion, Nicolas Andreu, Khaled Ezzedine, Thomas Darde, Katia Boniface, Julien Seneschal

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In one paragraph

Article in Journal of the European Academy of Dermatology and Venereology : JEADV, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Clinical heterogeneity in vitiligo: Identification of clinical markers based patient clusters.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Article
  2. 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

9 authors.

Laura GalissiCHU de Bordeaux, Department of Dermatology and Pediatric Dermatology, National Reference Center for Rare Skin Disorders, Hôpital Saint-André, Bordeaux, France.
Tristan BenoîtSciLicium, Rennes, France.
Ribal MerhiCHU de Bordeaux, Department of Dermatology and Pediatric Dermatology, National Reference Center for Rare Skin Disorders, Hôpital Saint-André, Bordeaux, France.
Claire DrullionUniv. Bordeaux, CNRS, ImmunoConcEpT, Bordeaux, France.
Nicolas AndreuCHU de Bordeaux, Department of Dermatology and Pediatric Dermatology, National Reference Center for Rare Skin Disorders, Hôpital Saint-André, Bordeaux, France.
Khaled EzzedineDepartment of Dermatology, Henri Mondor University Hospital, Créteil, France.ORCID https://orcid.org/0000-0002-5468-4589
Thomas DardeSciLicium, Rennes, France.
Katia BonifaceUniv. Bordeaux, CNRS, ImmunoConcEpT, Bordeaux, France.ORCID https://orcid.org/0000-0003-4428-1222
Julien SeneschalCHU de Bordeaux, Department of Dermatology and Pediatric Dermatology, National Reference Center for Rare Skin Disorders, Hôpital Saint-André, Bordeaux, France.ORCID https://orcid.org/0000-0003-1139-0908

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVitiligo (non-segmental) is a chronic autoimmune skin disease leading to white patches. Although vitiligo has been delineated previously, the endophenotypes of the disease are still to be defined.

objectivesThe aim of this study was to investigate, without prior hypotheses, whether different clinical phenotypes of vitiligo could be identified and differ based on their demographic and clinical characteristics.

methodsThis retrospective, non-interventional, single-centre study included patients with vitiligo. Demographic and clinical characteristics of vitiligo were recorded. Hierarchical cluster analysis was then performed.

resultsA total of 399 patients were included. The cluster analysis classified the patients into five clusters as follows: (1) 'highly active patients' with elevated frequency of disease activity signs, receiving combinatorial topical and systemic therapy; (2) mild vitiligo patients with younger patients, low surface area involved and absence of signs of disease activity; (3) extensive vitiligo patients, with older patients and the largest surface area involved; (4) and (5) mild or moderate to severe disease, with localization of the lesions on site of chronic skin friction (type 2A koebner phenomenon).

conclusionsPatients with vitiligo can be classified into five phenotypes, with two defining the highly active and extensive patients.

Indexed as

VitiligoAdolescentAdultAgedChildCluster AnalysisFemaleHumansMaleMiddle AgedPhenotypeRetrospective StudiesSeverity of Illness IndexYoung Adult

Identifiers

PMID40485245
PMCPMC13014437

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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 OpenQuestion graph.