Evidence map›Paper›PMID 36529602›Full record

ArticleAnais brasileiros de dermatologia

Experimental approaches to assess melanocytes mosaicism in segmental vitiligo.

Gerson Dellatorre, Vinicius M Fava, Marcelo Távora Mira, Caio Cesar Silva de Castro

Open access · goldAbstract read
In one paragraph

Article in Anais brasileiros de dermatologia. 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
0.5field-weighted citation impact, top 41% of its field
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, 5 citations in OpenAlex.

  1. Article
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

4 authors at 3 institutions in 2 countries.

Gerson DellatorreSanta Casa de Misericórdia Hospital, Curitiba, PR, Brazil.
Vinicius M FavaInfectious Diseases and Immunity in Global Health Program, The Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Marcelo Távora MiraSanta Casa de Misericórdia Hospital, Curitiba, PR, Brazil; Graduate Program in Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil; School of Life Sciences, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil.
Caio Cesar Silva de CastroSanta Casa de Misericórdia Hospital, Curitiba, PR, Brazil; School of Medicine, Pontifícia Universidade Católica do Paraná, Curitiba, PR, Brazil. Electronic address: caio.castro@pucpr.br.
Pontifícia Universidade Católica do Paraná · BRMcGill University Health Centre · CASanta Casa de Misericórdia de Passos · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitiligo is an autoimmune disease of the skin that results in localized or disseminated white macules. One common feature of several existing classification protocols is the distribution of the disease into two main subtypes, non-segmental vitiligo (NSV) and segmental vitiligo (SV). SV is characterized by depigmentation spreading within one or more skin segments while NSV is widespread. Several clinical-epidemiological observations suggest that SV has distinct autoimmune pathophysiology compared to NSV. Furthermore, the clinical distribution pattern of SV lesions closely resembles other melanocyte mosaicism diseases. These observations led us to hypothesize that SV is caused by a localized autoimmune reaction targeting epidermal mosaicism melanocytes. Here, we proposed examples of experimental approaches to assess mosaicism in SV patients.

Indexed as

VitiligoEpidermisHumansMelanocytesMosaicismSkinGeneticsMosaicismVitiligo

Identifiers

PMID36529602
PMCPMC9984711
OpenAlexW4311934120

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.